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[[Image:DNA-Animation.gif|thumb|220px|Three-dimensional model of the structure of part of a DNA double helix.]]
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Deoxyribonucleic acid (DNA) is a very large biological molecule found in almost every cell and is responsible for providing information required for the development and reproduction of living things. Every living organism has its own unique DNA sequence (code) similar to a 'barcode' or 'fingerprint'. This code, called a genome, is used primarily to control the synthesis of proteins. The important genetic discoveries in DNA research are the complementary duplex structure, often referred to as the "double-helix", that enables the accurate replication of DNA in living organisms, and that the internally coded, inheritible information defines the genotype which provides the necessary instructions to produce the phenotype, or outward physical manifestation an organism.[1]
''' DNA''' (''D''eoxyribo''n''ucleic ''a''cid) provides the genetic information necessary for the development and reproduction of all [[Life|living]] organisms and is often described as a genetic blueprint.<ref>All ''living'' organisms use DNA as their genetic material with the exception of some [[RNA viruses]]. Whether viruses are alive is also a [[Virus (biology)#Lifeform_debate|debatable question]] among biologists since they do not qualify based on some the the prerequisites for [[life]], such as having a [[metabolism]]].</ref>  <!--DNA is an enormously long and narrow biological [[molecule]] usually packaged in very compact structures called [[chromosome]]s which are located in the [[nucleus]] of a cell.
 
-->Every living organism has its own [[Genetic code|DNA code]] that is organized in the ladder-like structure of the DNA molecule as a series of complementary paired molecules called bases. DNA is found within the nucleus of many cells, including those of animal and plant life.
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DNA functions as a template: information is transferred from the sequence of base pairs within the DNA, by a molecule called messenger RNA (mRNA), to an enzyme called a [[ribosome]] (a biochemical assembly machine). The ribosome [[translation|translate]]s the code by assembling a [[protein]] molecule from [[amino acid]]s (the building blocks of proteins) according to the base pair sequence brought to it by the mRNA. Proteins are very complex molecules used for signaling, regulation, metabolism and structural components. [[Cell (biology)|Cell]]s containing DNA in any one organism have the same DNA, but each different cell type will synthesize its  own characteristic combination of proteins, some common to most cells, while others are more specialized and help to define the functions of that particular cell type.
 
It is the complementary structure of DNA which enables it to function as a template for translating the genetic code and the assembly of the proteins. This complementary structure also enables the double stranded DNA to be separated and replicated as two exact duplicates during cell division (replication). <ref>Kornberg, Arthur. ''DNA Replication''. W.H.Freeman and Co. (1980) "Complementarity has come to explain transcription and translation and thus the entire sequence of events in the expression of genetic functions. It is also the basis for exchange of DNA segments between chromosomes in several forms of recombination." </ref>
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{{Image|DNA_chemical_structure.png|right|280px|Shown here are the four "letters" of DNA.</onlyinclude> The complementary base pairs are red & yellow and blue & green. The sugars in the backbone are shown in light blue. The twin strands of DNA are held together by hydrogen bonds between bases in a ladderlike structure.  A codon is composed of a sequence of three of complementary base pairs. Each codon codes for one amino acid residue. It is a series of codons, along with a start codon and three stop codons that is transcribed and translated into a protein molecule. <onlyinclude>}}
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== Overview ==
In most organisms, DNA is formed as a very long and narrow double-helix formation of two DNA strands coiled around each other in a head-to-toe "antiparallel" orientation. The strands provide  structural support for a complementary pair of bases located between the strands (a base pair is like a letter of a genetic word). A sequence of three base pairs forms a codon (a DNA word) on the DNA strand that encodes the information for one amino acid residue. A series of codons, and associated start/stop codons (a DNA sentence or gene), form the genetic code for the selection of particular amino acids and their specific arrangement necessary for the assembly of a particular protein molecule. The protein molecules, as many as 20,000 different types, are used in the cell, or are transported, often via small containers (vesicles), to other areas of the organism. 
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Each single strand of DNA is a long biopolymer composed of repeating units called [[nucleotide]]s.  A nucleotide is a base linked to a sugar and phosphate group which form a sugar/phosphate backbone.  Attached to each sugar molecule (deoxyribose) is one of the four ''[[Nucleobase|bases]]'':
* [[Adenine]] (A)<ref name=Adenin>[https://hmdb.ca/metabolites/HMDB0000034 Adenine (HMDB0000034)] in the Human Metabolome Database (HMDB).</ref>
* Thymine (T)<ref name=Thymin>[https://hmdb.ca/metabolites/HMDB0000262 Thymine (HMDB0000262)] in the Human Metabolome Database (HMDB).</ref>
* [[Guanine]] (G)<ref name=Guanin>[https://hmdb.ca/metabolites/HMDB0000132 Guanine (HMDB0000132)] in the Human Metabolome Database (HMDB).</ref>
* Cytosine (C)<ref name=Cytosin>[https://hmdb.ca/metabolites/HMDB0000630 Cytosine (HMDB0000630)] in the Human Metabolome Database (HMDB).</ref>
 
The corresponding deoxynucleosides are:
* Deoxyadenosine<ref name=Deoxyaden>[https://hmdb.ca/metabolites/HMDB0000101 Deoxyadenosine (HMDB0000101)] in the Human Metabolome Database (HMDB).</ref>
* Thymidine<ref name=Thymid>[https://hmdb.ca/metabolites/HMDB0000273 Thymidine (HMDB0000273)] in the Human Metabolome Database (HMDB).</ref>
* Deoxyguanosine<ref name=Deoxyguan>[https://hmdb.ca/metabolites/HMDB0000085 Deoxyguanosine (HMDB0000085)] in the Human Metabolome Database (HMDB).</ref>
* Deoxycytidine<ref name=Deoxycyt>[https://hmdb.ca/metabolites/HMDB0000014 Deoxycytidine (HMDB0000014)] in the Human Metabolome Database (HMDB).</ref>
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Double-stranded DNA is formed by a weak [[hydrogen bond]] between the bases holding the nucleotides  together. Each base is a structural complement of its opposing base, so both together form the base pair. The complementarity base pairs, A&T,  C&G, are identical in size and shape and  only one of the four arrangements - TA, AT, GC and CG, will fit between the backbones of double stranded DNA;  e.g., adenine always pairs with thymine and guanine always pairs with cytosine. This ''complementarity'', is at work in all DNA functions, and makes it possible for DNA to be copied and repaired relatively easily, while accurately preserving its information content. Thus it forms the basis of "semi-conservative DNA replication".<ref name=?>[https://www.nature.com/scitable/topicpage/semi-conservative-dna-replication-meselson-and-stahl-421/ Pray, L. (2008) Semi-conservative DNA replication: Meselson and Stahl. Nature Education 1(1):98]</ref> {{TOC|left}}<onlyinclude>
 
Nuclear DNA is organized and stored as [[chromosome]]s within the nucleus. The nucleus is a double membrane separating the DNA from the cytoplasm of the cell enabling certain processing to occur prior to protein synthesis. Each chromosome holds hundreds or thousands of genes. A gene can be described in different ways but in general can be thought of as a whole unit of genetic information.
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At conception for the human animal, the male sperm (a half-stranded DNA with a protein coat), and female ovum (an unfertilized egg also containing a single strand of DNA), each contribute 23 chromosomes for a total of 46 chromosomes in the fertilized embryo. The total sum of chromosomes is called the karyotype in [[eukaryote]]s (organisms such as plants, yeasts and animals whose cells have a nucleus)
 
Some organelles in eukaryotic cells ([[mitochondrion|mitochondria]] and [[chloroplast]]s) have their own DNA with a similar organization to bacterial genomes. This DNA encodes for some of the functions in these organelles. Both the mitochondrial DNA (mtDNA) and the chloroplast DNA (cpDNA) originate in the female egg, so the organelle DNA is always inherited from the mother. Some cells, such as blood cells, do not have a nucleus and do not contain DNA. In prokaryote cells (organisms such as common bacteria), DNA is located in a region called the ''nucleoid''. [[Virus]]es have a single type of [[nucleic acid]], either DNA or RNA, directly encased in a protein coat called the capsid.
 
The entire DNA sequence of genes as a whole in any organism is called its [[genome]]. The genome provides the necessary genetic instructions to produce the [[phenotype]], the outward physical manifestation of an organism, as well as the necessary processes involved in the replication of nuclear DNA.
 
==Seeking the secret of life==
Important genetic discoveries in DNA research spanned many decades. It was taken for granted by early researchers that only a protein molecule was complex enough to contain genetic information. A major discovery included the unexpected realization that the seemingly simple DNA molecule, and not the more complex protein molecule, is responsible for the internally coded, inheritable information defining the [[genotype]].  A further significant discovery was that the paired bases exist in equal proportions. These initial discoveries led to the important discovery of the duplex structure of DNA, usually referred to as the "''double-helix''", that enables the complementary replication of DNA in living organisms.  The most important feature of the duplex model is the introduction of the concept of complementarity. Complementarity has come to explain the entire sequence of events in the expression of genetic functions.<ref>Kornberg, Arthur. ''DNA Replication''. W.H.Freeman and Co. (1980) p13</ref>


====Isolating genetic material====
DNA was first isolated in 1869 by [[Friedrich Miescher]] who discovered a microscopic substance in the pus of discarded surgical bandages. Because it resided in the nuclei of cells, he called it "nuclein".<ref>{{cite journal | author = Dahm R | title = Friedrich Miescher and the discovery of DNA | journal = Dev Biol | volume = 278 | pages = 274-88 | year = 2005 | id = PMID 15680349}}</ref> In 1929, [[Phoebus Levene]]'s identified  the base, sugar and phosphate nucleotide unit  .<ref>{{cite journal|author = Levene P|title = The structure of yeast nucleic acid | url=http://www.jbc.org/cgi/reprint/40/2/415|journal = J Biol Chem|volume = 40|pages = 415-24 | year = 1919}}</ref> Levene suggested that DNA consisted of a string of nucleotide units linked together through the phosphate groups. However Levene thought the chain was short and the bases repeated in a fixed order.


In 1928, [[Frederick Griffith]] demonstrated a "transforming factor" that can transmit the ability of ''Pneumococcus'' bacteria to cause pneumonia in mice. Although DNA had been identified in cells, it was not considered a strong candidate for the genetic material due to its simple form. 


DNA is a long [[polymer]] comprised of simple units called [[nucleotides]] which are held together by a [[sugar]] [[phosphate]] backbone (called a nucleoside). Attached to each sugar molecule ([[deoxyribose]]) is a molecule of one of four ''[[bases]]''; [[Adenine]] (A), [[Thymine]] (T), [[Guanine]] (G) or [[Cytosine]] (C). Each base is complemented by the opposing base.  Because of the chemical and physical structure of these bases, adenine always pairs with thymine and guanine always pairs with cytosine. These pairs are identical in size and shape and will fit between the backbones in any configuration. Each base pair can have one of four configurations TA, AT, GC and CG. It is the sequence of at least three of these base pairs that form a codon on the DNA strand that encodes the information. This ''complementarity'' forms the basis of [[semi-conservative DNA replication]] &mdash; making it possible for DNA to be copied relatively easily, while accurately preserving its information content. A series of condons then make up a gene. The series of genes make up the chromosome. There are 23 pairs of chromosomes in a typical human cell.  
In 1943, [[Oswald Theodore Avery]] extended Griffith's work and discovered that traits of the virulent form of ''Pneumococcus'' could be transferred to the avirulent form of the same bacteria by mixing killed virulent bacteria with the live avirulent form. Avery identified DNA as the ''transforming factor''.<ref>{{cite journal | author = Avery O, MacLeod C, McCarty M | title = Studies on the chemical nature of the substance inducing transformation of pneumococcal types. Inductions of transformation by a desoxyribonucleic acid fraction isolated from pneumococcus type III | url=http://www.jem.org/cgi/reprint/149/2/297 | journal = J Exp Med | volume = 149 | issue = 2 | pages = 297-326 | year = 1979 | id = PMID 33226}}</ref> This discovery is considered by some to be a major breakthrough enabling new research methods and a new focus on DNA itself and therefore represents the birth of [[molecular biology]].<ref>Asimov, Isaac. (1962) The Genetic Code. pg viii New American Library. Written while he was Associate Professor of Biochemistry at Boston University School of Medicine. "It launched in a new direction the investigation into the nature of life and brought about a new research methods. The branch of science now called "molecular biology" came into its own."</ref>
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In most organisms, DNA is in a double-helix formation consisting of two DNA strands coiled around each other, in a head-to-tail "antiparallel" orientation, held together by [[hydrogen bonds]] between bases on opposing strands. The entire DNA sequence of genes in any organism is called its [[genome]]. DNA replicates by separating the hydrogen bonds between the strands and then (reattaching) the/a complementary molecule to each separate strand resulting in two identical copies.


In animals and plants, most DNA is stored inside the [[cell nucleus]]. In [[bacteria]], there is no nuclear membrane around the DNA, which is in a region called the ''[[nucleoid]]''. Some organelles in eukaryotic cells ([[mitochondria]] and [[chloroplast]]s) have their own DNA with a similar organisation to bacterial DNA. [[Viruses]] have a single type of [[nucleic acid]], either DNA or RNA, directly encased in a [[protein]] coat called the [[capsid]].
DNA's role in heredity was confirmed in 1953, when [[Alfred Hershey]] and [[Martha Chase]] in the [[Hershey-Chase experiment]], showed that DNA is the [[genetic material]] of the [[T2 phage]].<ref>{{cite journal | author = Hershey A, Chase M | title = Independent functions of viral protein and nucleic acid in growth of bacteriophage | url=http://www.jgp.org/cgi/reprint/36/1/39.pdf | journal = J Gen Physiol | volume = 36 | issue = 1 | pages = 39-56 | year = 1952 | id = PMID 12981234}}</ref> This experiment provided the  crucial evidence that it was DNA itself, (which was shown to enter the cell), and not a protein,(which remained outside the cell), that was the carrier of information.


== History of DNA ==
====Discovering the double helix and code====
DNA was first isolated by [[Friedrich Miescher]] who, in 1869, discovered a microscopic substance in the pus of discarded surgical bandages. As it resided in the nuclei of cells, he called it "nuclein".<ref>{{cite journal | author = Dahm R | title = Friedrich Miescher and the discovery of DNA | journal = Dev Biol | volume = 278 | issue = 2 | pages = 274-88 | year = 2005 | id = PMID 15680349}}</ref> In 1929 this discovery was followed by [[Phoebus Levene]]'s identification of the base, sugar and phosphate nucleotide unit.<ref>{{cite journal | author = Levene P, | title = The structure of yeast nucleic acid | url=http://www.jbc.org/cgi/reprint/40/2/415 | journal = J Biol Chem | volume = 40 | pages = 415-24 | year = 1919}}</ref> Levene suggested that DNA consisted of a string of nucleotide units linked together through the phosphate groups. However Levene thought the chain was short and the bases repeated in a fixed order. In 1937 [[William Astbury]] produced the first [[X-ray diffraction]] patterns that showed that DNA had a regular structure.<ref>{{cite journal | author =Astbury W, | title = Nucleic acid | journal = Symp. Soc. Exp. Biol | volume = 1 | issue = 66 | year = 1947}}</ref>
In 1950, Erwin Chargaff published a paper in which he described something he found extraordinary: the ratios of adenine to thymine were equal, as well as cytosine to guanine. He called this ''the complementary situation'', but later it became known as the ''Chargaff Ratios''This discovery would  play a crucial role in determining the structure of DNA. <ref>Interview of Chargaff at DNA interactive web site.</ref>


In 1943, [[Oswald Theodore Avery]] discovered that traits of the "smooth" form of the ''Pneumococcus'' could be transferred to the "rough" form of the same bacteria by mixing killed "smooth" bacteria with the live "rough" form. Avery identified DNA as this [[transforming principle]].<ref>{{cite journal | author = Avery O, MacLeod C, McCarty M | title = Studies on the chemical nature of the substance inducing transformation of pneumococcal types. Inductions of transformation by a desoxyribonucleic acid fraction isolated from pneumococcus type III | url=http://www.jem.org/cgi/reprint/149/2/297 | journal = J Exp Med | volume = 149 | issue = 2 | pages = 297-326 | year = 1979 | id = PMID 33226}}</ref>
As early as 1937, William Astbury produced the first [[X-ray diffraction]] patterns that showed that DNA had a regular structure.<ref>{{cite journal | author =Astbury W | title = Nucleic acid | journal = Symp Soc Exp Biol | volume = 1 | | year = 1947}}</ref> But it was not until 1953, based on the high-quality X-ray diffraction images<ref name=FWPUB>Watson JD, Crick FHC (1953) A structure for deoxyribose nucleic acid. 'Nature'' [http://www.nature.com/nature/dna50/watsoncrick.pdf 171:737–8] Accessed 13 Feb 2007.</ref> taken by Rosalind Franklin and the information provided by Erwin Chargaff that the bases were paired, that [[James D. Watson]] and [[Francis Crick]] constructed a cardboard model that led to <ref name=FWPUB/> what is now accepted as the first accurate model of [[Molecular structure of Nucleic Acids|DNA structure]]. Their discovery on the morning of February 28, 1953, was reported in the journal ''Nature''.<ref name=Watson>{{cite journal | author = Watson J, Crick F | title = Molecular structure of nucleic acids; a structure for deoxyribose nucleic acid | url=http://profiles.nlm.nih.gov/SC/B/B/Y/W/_/scbbyw.pdf | journal = Nature | volume = 171 | pages = 737-8 | year = 1953 | id = PMID 13054692}}</ref>


In 1950, Erwin Chargaff published a paper in which he described the equal ratios of adenine to thymine, as well as cytosine to guanine, something he found extraordinary, and which he called the complementary situation, but later was known as the Chargaff Ratios  This discovery would  play a crucial role in determining the structure of DNA.  
Experimental evidence for Watson and Crick's model was published in five articles in the same issue of ''Nature''.<ref name=NatureDNA50>Nature Archives [http://www.nature.com/nature/dna50/archive.html Double Helix of DNA: 50 Years]</ref> Of these, Franklin and Raymond Gosling's paper<ref name=NatFranGos> Franklin R, Gosling RG (1953)Molecular configuration in sodium thymonucleate. ''Nature'' [http://www.nature.com/nature/dna50/franklingosling.pdf N 171, 740–1]</ref> saw the publication of the X-ray diffraction image <ref>[http://osulibrary.oregonstate.edu/specialcollections/coll/pauling/dna/pictures/franklin-typeBphoto.html Original X--ray diffraction image]</ref>, which was key in Watson and Crick's interpretation, as well as another article, co-authored by Maurice Wilkins and his colleagues.<ref name=NatWilk>  Wilkins MHF, Stokes AR, Wilson HR (1953) Molecular structure of deoxypentose nucleic acids.''Nature'' [http://www.nature.com/nature/dna50/wilkins.pdf 171:738–40 </ref> Franklin and Gosling's subsequent paper identified the distinctions between the A and B structures of the double helix in DNA.<ref name=NatFrankGos2> Franklin R, Gosling RG (1953) Evidence for 2-chain helix in crystalline structure of Sodium Deoxyribonucleate. ''Nature'' [http://www.nature.com/nature/dna50/franklingosling2.pdf 172:156–7]</ref> In 1962, Watson, Crick, and Maurice Wilkins jointly received the [[Nobel Prize]] in [[Nobel Prize in Physiology or Medicine|Physiology or Medicine]] (Franklin didn't share the prize with them as she had died earlier).<ref>[http://nobelprize.org/nobel_prizes/medicine/laureates/1962/ The Nobel Prize in Physiology or Medicine 1962] Nobelprize .org Accessed 22 Dec 06</ref>


DNA's role in heredity was confirmed in 1953, when [[Alfred Hershey]] and [[Martha Chase]] in the [[Hershey-Chase experiment]], showed that DNA is is the [[genetic material]] of the [[T2 phage]].<ref>{{cite journal | author = Hershey A, Chase M | title = Independent functions of viral protein and nucleic acid in growth of bacteriophage | url=http://www.jgp.org/cgi/reprint/36/1/39.pdf | journal = J Gen Physiol | volume = 36 | issue = 1 | pages = 39-56 | year = 1952 | id = PMID 12981234}}</ref>
In an influential presentation in 1957, Crick laid out the "central dogma" of molecular biology, which foretold the relationship between DNA, RNA, and proteins and articulated the "adaptor hypothesis".<ref>Crick FHC (1955) On degenerate templates and the adaptor hypothesis[http://genome.wellcome.ac.uk/assets/wtx030893.pdf  (PDF)] genome.wellcome.ac.uk (Accessed 22 Dec 2006</ref> Final confirmation of the replication mechanism that was implied by the double-helical structure followed in 1958 through the [[Meselson-Stahl experiment]].<ref>{{cite journal | author = Meselson M, Stahl F | title = The replication of DNA in Escherichia coli | journal = Proc Natl Acad Sci USA | volume = 44 | pages = 671-82 | year = 1958 | id = PMID 16590258}}</ref> Further work by Crick and coworkers showed that the genetic code was based on non-overlapping triplets of bases, called codons, allowing [[Har Gobind Khorana]], [[Robert W. Holley]] and [[Marshall Warren Nirenberg]] to decipher the [[genetic code]].<ref>[http://nobelprize.org/nobel_prizes/medicine/laureates/1968/ The Nobel Prize in Physiology or Medicine 1968] Nobelprize.org Accessed 22 Dec 06</ref>
This experiment provided the crucial evidence that it was DNA itself, which was shown to enter the cell, and not a protein, which remained outside the cell, that was the carrier of information. But the structure of DNA remained unknown.  


In 1953, based on [[Photo 51|X-ray diffraction images]]<ref name=FWPUB>Watson J.D. and Crick F.H.C. [http://www.nature.com/nature/dna50/watsoncrick.pdf "A Structure for Deoxyribose Nucleic Acid".] (PDF) ''Nature'' 171, 737 – 738 (1953). Accessed 13 Feb 2007.</ref> taken by [[Rosalind Franklin]] and the information provided by Erwin Chargaff that the bases were paired, [[James D. Watson]] and [[Francis Crick]] constructed a cardboard model that led to <ref name=FWPUB/> what is now accepted as the first accurate model of [[Molecular structure of Nucleic Acids|DNA structure]] in the journal [[Nature (journal)|''Nature'']].<ref name=Watson/>
==== Big science: the Human Genome Project====
Initially biologists could only clone and sequence genes one by one, which required large amounts of labor and time in laboratories that were in scattered locations. As technology improved in the 1980's, some scientists such as [[Craig Venter]] and [[Leroy Hood]] believed their research could focus on sequencing whole genomes and they advocated a era of big science epitomised by the [[Human Genome Project]] (HGP). Their goal was to automate the mapping and sequencing to produce resources that would give science a valuable shortcut to addressing the biology of the genome.  


Experimental evidence for Watson and Crick's model were published in a series of five articles in the same issue of ''Nature''.<ref name=NatureDNA50>Nature Archives [http://www.nature.com/nature/dna50/archive.html Double Helix of DNA: 50 Years]</ref> Of these, [[Rosalind Franklin|Franklin]] and [[Raymond Gosling]]'s paper<ref name=NatFranGos>Molecular Configuration in Sodium Thymonucleate. Franklin R. and Gosling R.G.Nature 171, 740 – 741 (1953)[http://www.nature.com/nature/dna50/franklingosling.pdf Nature Archives Full Text (PDF)]</ref> saw the publication of the X-ray diffraction image <ref>[http://osulibrary.oregonstate.edu/specialcollections/coll/pauling/dna/pictures/franklin-typeBphoto.html Original X--ray diffraction image]</ref>, which was key in Watson and Crick interpretation, as well as another article, co-authored by [[Maurice Wilkins]] and his colleagues.<ref name=NatWilk>Molecular Structure of Deoxypentose Nucleic Acids. Wilkins M.H.F., A.R. Stokes A.R. & Wilson, H.R. Nature 171, 738 – 740 (1953)[http://www.nature.com/nature/dna50/wilkins.pdf Nature Archives (PDF)]</ref> Franklin and Gosling's subsequent paper identified the distinctions between the A and B structures of the double helix in DNA.<ref name=NatFrankGos2>Evidence for 2-Chain Helix in Crystalline Structure of Sodium Deoxyribonucleate. Franklin R. and Gosling R.G. Nature 172, 156 – 157 (1953)[http://www.nature.com/nature/dna50/franklingosling2.pdf Nature Archives, full text (PDF)]</ref> In 1962 Watson, Crick, and [[Maurice Wilkins]] jointly received the [[Nobel Prize]] in [[Nobel Prize in Physiology or Medicine|Physiology or Medicine]] (Franklin didn't share the prize with them since she had died earlier).<ref>[http://nobelprize.org/nobel_prizes/medicine/laureates/1962/ The Nobel Prize in Physiology or Medicine 1962] Nobelprize .org Accessed 22 Dec 06</ref>
Leroy Hood designed DNA sequencing machines to automate the process and thus massively reduce the cost of large scale sequencing. The chemistry of dideoxy sequencing devised by [[Frederick Sanger]] in 1977 was still the primary tool but new fluorescent labeling techniques, polymerase chain reaction ([[PCR]]) and genomic [[BAC]]/[[YAC]] libraries, were technological advances that made automation possible. Craig Venter advocated a random "shotgun" approach in the form of sequencing a massive number of randomly picked expressed sequence tags ([[EST]]'s). Each tag represented a cDNA clone and the whole collection represented a catalog of expressed genes in a genome. This approach transitioned to sequencing random BAC's from the whole genome and was coined [[shotgun sequencing]].  


In an influential presentation in 1957, Crick laid out [[the "central dogma" of molecular biology]], which foretold the relationship between DNA, RNA, and proteins, and articulated the "adaptor hypothesis".<ref>Crick FHC [http://genome.wellcome.ac.uk/assets/wtx030893.pdf On degenerate templates and the adaptor hypothesis (PDF).] genome.wellcome.ac.uk (Lecture, 1955). Accessed 22 Dec 2006</ref> Final confirmation of the replication mechanism that was implied by the double-helical structure followed in 1958 through the [[Meselson-Stahl experiment]].<ref>{{cite journal | author = Meselson M, Stahl F | title = The replication of DNA in Escherichia coli | journal = Proc Natl Acad Sci USA | volume = 44 | pages = 671-82 | year = 1958 | id = PMID 16590258}}</ref> Further work by Crick and coworkers showed that the genetic code was based on non-overlapping triplets of bases, called codons, allowing [[Har Gobind Khorana]], [[Robert W. Holley]] and [[Marshall Warren Nirenberg]] to decipher the [[genetic code]].<ref>[http://nobelprize.org/nobel_prizes/medicine/laureates/1968/ The Nobel Prize in Physiology or Medicine 1968] Nobelprize.org Accessed 22 Dec 06</ref> These findings represent the birth of [[molecular biology]].
The HGP started out as an academic pursuit that used the traditional and slower target driven approach, a methodological tactic of establishing unique genetic markers, breaking the DNA into smaller bits which were then sequenced and, using the markers as a guide, reassembled. The public consortium was joined by a private effort at Celera Genomics that used the shotgun sequencing approach and a race to finish the project ensued. With the use of computers the vast number of fragments from Celera were assembled using the framework established by the HGP and in June of 2000, the completion of the draft sequence was announced by the leaders of the public and private projects. In January of 2008, the 1000 Genome Project, a mapping of 1000 genomes, was announced.


==Overview of biological functions==
==Assembled according to code==
DNA contains the genetic information that is the basis for living functions including growth, reproduction and evolution. This information is held in segments of the DNA called ''genes'' that may span in size from scores of DNA base-pairs to many thousands of base-pairs. DNA usually occurs as several large, linear [[chromosome]]s, each of which may contain hundreds or thousands of genes in [[eukaryotes]] (organisms such as plants, yeasts and animals whose cells have a nucleus). The set of chromosomes in a cell makes up its [[genome]]; the [[human genome]] has about three billion base pairs of DNA arranged into 46 chromosomes <ref name=Venter>{{cite journal | author = Venter J ''et al.'' | title = The sequence of the human genome | journal = Science | volume = 291 | pages = 1304–51 | year = 2001 | id = PMID 11181995}}</ref> and contains 20-25,000 genes<ref>Human Genome Project Information [http://www.ornl.gov/sci/techresources/Human_Genome/home.shtml]</ref>. [[Prokaryotes]] (organisms such as common bacteria) generally have a single large circular chromosome, but they often possess other miniature chromosomes called [[plasmid]]s.
[[Image:DNA-Animation.gif|thumb|220px|Three-dimensional model of the structure of part of a DNA double helix.]]
There are many interactions that happen between DNA and other molecules to coordinate its functions.
DNA is structured as a tightly-associated repeating pair of molecules (nucleotides) <ref name=Watson/><ref name=berg>Berg J ''et al.'' (2002) ''Biochemistry.'' WH Freeman and Co. ISBN 0-7167-4955-6</ref> entwined in the shape of a [[helix|double helix]]. Looking much like a ladder, a typical DNA strand is about 5cm long and only a few atoms in width. The nucleotide  repeats contain both the backbone of the molecule, which holds the chain together, and a base, which is a complement of the other DNA strand's base and backbone.  
When cells divide, the genetic information must be duplicated to produce two complementary copies of DNA in a process called ''[[DNA replication]]''. When a cell uses the information in a gene, the DNA sequence is copied into a complementary single strand of [[RNA]] in a process called ''[[transcription]]''. Of the transcribed sequences, some are used to directly make a matching protein sequence by a process called ''[[translation]]'' (meaning translation from a nucleic acid polymer to an [[amino acid]] polymer). The other transcribed RNA sequences may have regulatory, structural or catalytic roles.  


===Replication===
====Building blocks====
{{further|[[Replication of a circular bacterial chromosome]]}}
The backbone of the DNA strand has alternating phosphate and sugar residues<ref name=Ghosh>{{cite journal | author = Ghosh A, Bansal M | title = A glossary of DNA structures from A to Z | journal = Acta Crystallogr D Biol Crystallogr | volume = 59 | pages = 620-6 | year = 2003 | id = PMID 12657780}}</ref>: the sugar is the [[pentose]] (five carbon) sugar 2-deoxyribose. One of the major differences between DNA and RNA is the sugar: 2-deoxyribose is replaced by [[ribose]] in RNA.
[[Image:DNAreplicationFORK.jpg|thumb|400px| '''DNA-replication''' illustrated by the bacterial [[replication fork]]. The helix unwinds and both strands replicate simultaneously as they unwind. The ''[[leading strand]]'' replicates continuously from the 3' end, with the newest end of the forming strand facing into the replication fork. The ''[[lagging strand]]'' replicates by a series of fragments ([[Okazaki fragments]] placed end-to-end, with the newest ends  facing away from the fork; the Okazaki fragments are later joined together by DNA ligase. During replication, DNA polymerase III proofreads for mismatched bases]]


For an organism to grow, its cells must multiply, and this occurs by [[cell division]]: one cell splits to create two new 'daughter' cells. When a cell divides it must replicate its DNA so that the two daughter cells have the same genetic information as the parent cell. The double-stranded structure of DNA provides a simple mechanism for this replication. The two strands of DNA separate, and then each strand's complementary DNA sequence is recreated by an enzyme called [[DNA polymerase]]. This makes the complementary strand by finding the correct base (through complementary base pairing), and bonding it to the original strand. DNA polymerases can only extend a DNA strand in a 5' to 3' direction, so other mechanisms are needed to copy the antiparallel strands of the double helix.<ref>{{cite journal | author = Albà M | title = Replicative DNA polymerases | url=http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=11178285 | journal = Genome Biol | volume = 2 | pages = REVIEWS3002 | year = 2001 | id = PMID 11178285}}</ref> In this way, the base on the old strand dictates which base appears on the new strand, and the cell (usually) ends up with a perfect copy of its DNA. However, occasionally mistakes (called [[mutation]]s) occur, contributing to the [[genetic variation]] that is the raw material for evolutionary change.  
The sugar molecules are joined together by phosphate groups that form [[phosphodiester bond]]s between the third and fifth carbon atoms in the sugar rings. A strand of DNA has a 'direction'. In a double helix, the direction of the nucleotides in one strand is opposite to that in the other strand. Because these bonds are asymmetric, this arrangement of DNA strands is called ''antiparallel''. The asymmetric ends of a strand of DNA bases are referred to as the [[5' end|5']] (''five prime'') and [[3' end|3']] (''three prime'') ends.  


DNA replication requires a complex set of proteins, each dedicated to one of several different tasks needed to replicate this large molecule in an orderly and precise fashion. Further capacity for DNA replication with substantial rearrangement (which has major implications for understanding mechanisms of [[molecular evolution]], is provided by mechanisms for DNA movement, inversion, and duplication, illustrated by various [[Mobile DNA|mobile DNA]]s such as [[transposons]] and [[proviruses]].
The double helix is a right-handed spiral. As the DNA strands wind around each other, gaps, called the major and a minor grooves, between the two phosphate backbones reveal the sides of the bases inside (see animation). Two grooves twist around the surface of the double helix: the major groove is 22&nbsp;Å wide and the minor groove is 12&nbsp;Å wide.<ref>{{cite journal | author = Wing R ''et al.''|title = Crystal structure analysis of a complete turn of B-DNA | journal = Nature|volume = 287|pages = 755–8|year = 1980|id = PMID 7432492}}</ref> The edges of the bases are more accessible in the major groove, so proteins like [[transcription factor]]s that can bind to specific sequences in double-stranded DNA usually make contacts to the sides of the bases exposed in the major groove. <ref name=Pabo>{{cite journal | author = Pabo C, Sauer R| title = Protein-DNA recognition|journal = Ann Rev Biochem|volume = 53|pages = 293-321 | year = | id = PMID 6236744}}</ref>  For many DNA: protein complexes, up to one-half of the contacts involve the DNA phosphate groups, and thus many DNA binding proteins have more positive amino acids (lysine and arginine) than usual.  


===Transcription and translation===
The double helix is held together by weak [[hydrogen bond]]s between the complementary bases attached to the two strands. If many nucleotides are linked together, as in DNA, the [[polymer]] is referred to as a [[polynucleotide]].<ref name=IUPAC>[http://www.chem.qmul.ac.uk/iupac/misc/naabb.html Abbreviations and Symbols for Nucleic Acids, Polynucleotides and their Constituents] IUPAC-IUB Commission on Biochemical Nomenclature (CBN) Accessed 03 Jan 2006</ref>
Within most (but not all) genes, the nucleotides define a [[messenger RNA]] (mRNA) which in turn defines one or more protein sequences. This is possible because of the [[genetic code]] which [[Translation (genetics)|translate]]s the nucleic acid sequence to an [[amino acid|amino-acid]] sequence. The genetic code consists of three-letter 'words' called ''[[codon]]s'' formed from a sequence of three nucleotides. For example, the sequences ACU, CAG and UUU in mRNA are translated to threonine, glutamine and phenylalanine, respectively.


In transcription, the codons are copied into mRNA by [[RNA polymerase]]. This copy is then decoded by a [[ribosome]] that reads the RNA sequence by base-pairing the mRNA to a specific [[aminoacyl-tRNA]]; an amino acid carried by a [[transfer RNA]] (tRNA). As there are four bases in three-letter combinations, there are 64 possible codons, and these encode the twenty [[list of standard amino acids|standard amino acids]]. Most amino acids, therefore, have more than one possible codon (for example, ACU and ACA both code for threonine). There is one start codon (AUG, which also encodes for [[methionine]]) and three 'stop' or 'nonsense' codons (UAA, UGA and UAG) that signify the end of the coding region.
==== Base pairing ====
Each type of base on one strand of DNA forming a bond with a complementary base on the other strand, is called [[base pair]]ing'. Purines form hydrogen bonds to pyrimidines; for example, A bonds only to T, and C bonds only to G. This arrangement of two nucleotides joined together across the double helix is called a ''base pair''.  


===Genes===
The four bases in DNA are adenine (A), cytosine (C), guanine (G) and thymine (T), and these bases are attached to the sugar/phosphate to form the complete nucleotide. Adenine and guanine are fused five- and six-membered [[heterocyclic compound]]s called [[purine]]s, while cytosine and thymine are six-membered rings called [[pyrimidine]]s.<ref name=IUPAC/> A fifth pyrimidine base, [[uracil]] (U), replaces thymine in RNA. Uracil is normally only found in DNA as a breakdown product of cytosine, but [[phage|bacterial viruses]] contain uracil in their DNA.<ref name="nature1963-takahashi">{{cite journal | author=Takahashi I, Marmur J | title=Replacement of thymidylic acid by deoxyuridylic acid in the deoxyribonucleic acid of a transducing phage for Bacillus subtilis | journal=Nature | year=1963 | pages=794-5 | volume=197 | id=PMID 13980287}}</ref> In contrast, following synthesis of certain RNA molecules, many uracils are converted to thymines. This occurs mostly on structural and enzymatic RNAs like tRNAs and [[ribosomal RNA]].<ref>{{cite journal |author=Agris P |title=Decoding the genome: a modified view |
Our understanding of the various ways in which genes play a role in cells has been continually revised throughout the history of genetics, starting from abstract concepts of inheritable particles whose composition was unknown. This has led to several modern different definitions of a gene. One way to define a gene is simply as a segment of DNA that is transcribed into RNA - that is - ''the gene is a unit of transcription''. This definition encompasses genes for non-translated RNAs, such as [[ribosomal RNA]] ([[rRNA]]) and [[transfer RNA]] ([[tRNA]]), as well as [[messenger RNA]] ([[mRNA]]) which ''is'' used for encoding the sequences of proteins.
url=http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=14715921 |journal=Nucleic Acids Res |volume=32 |pages=223 – 38 |year=2004 |pmid=14715921}}</ref>


A second approach is to define a gene as ''a region of DNA that encodes a single polypeptide''. By this definition, any particular mRNA transcription unit can cover more than one gene, and thus a mRNA can carry regions encoding one or more polypeptides. Such a multi-genic transcription unit is called an [[operon]].
In a double helix, the two strands are also held together by [[hydrophobic effect]]s and by a variation of [[pi stacking]].<ref>{{cite journal | author = Ponnuswamy P, Gromiha M| title = On the conformational stability of oligonucleotide duplexes and tRNA molecules |journal = J Theor Biol|volume = 169|pages = 419-32|year = 1994|id = PMID 7526075}}</ref> Hydrogen bonds are weak, and can be broken and rejoined quite easily, so the two strands of DNA in a double helix can be pulled apart like a zipper, either by  mechanical force or by high temperatures.<ref>{{cite journal | author = Clausen-Schaumann H ''et al.'' | title = Mechanical stability of single DNA molecules | url=http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=1300792&blobtype=pdf | journal = Biophys J | volume = 78 |  pages = 1997-2007 | year = 2000 | id = PMID 10733978}}</ref> Usually the strands are separated by a helicase, a biological unwinding motor. Because the base pairs form a complementarity, the information in the double-stranded sequence of a DNA helix is duplicated on each of the separate complementary opposing strands. The reversible and specific interaction between complementary base pairs is vital in DNA replication. and is critical for all the functions of DNA in living organisms.


Other definitions include considering genes as ''units of biological function''. This definition can include sites on DNA that are not transcribed, such as DNA sites at which regulatory and catalytically active proteins concerned with gene regulation and expression are located. Examples of such sites (loci, sing. locus) are [[promoter]]s and [[operator]]s. ([[Locus (Genetics)|Locus]] is a genetic term very similar in meaning to gene, and which refers to a site or region on a chromosome concerned with a particular function or trait.)
The two types of base pairs form different numbers of hydrogen bonds; A&T forms two hydrogen bonds, and G&C forms three, so the G&C base-pair is stronger than the A&T pair. Thus, long DNA helices with a high G&C content have strongly interacting strands, while short helices with high A&T content have weakly interacting strands.<ref>{{cite journal | author = Chalikian T ''et al.''| title = A more unified picture for the thermodynamics of nucleic acid duplex melting: a characterization by calorimetric and volumetric techniques | url=http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=22151&blobtype=pdf | journal = Proc Natl Acad Sci USA | volume = 96 | pages = 7853-8 | year = 1999 | id = PMID 10393911}}</ref> Parts of the DNA double helix that need to separate easily tend to have a high A&T content, making the strands easier to pull apart.<ref>{{cite journal | author = deHaseth P, Helmann J | title = Open complex formation by Escherichia coli RNA polymerase: the mechanism of polymerase-induced strand separation of double helical DNA | journal = Mol Microbiol | volume = 16 | pages = 817-24 | year = 1995 | id = PMID 7476180}}</ref> The strength of this interaction can be measured by finding the temperature required to break the hydrogen bonds (their '[[melting temperature]]'). When all the base pairs in a DNA double helix melt, the strands separate, leaving two single-stranded molecules in solution.  Because base-pairing causes changes in the UV-visible spectrum of the bases, DNA melting can be monitored by observing the hypochronicity (or loss thereof) as a function of temperature. These molecules have no single shape, but some conformations are more stable than others.


All of the cells in our body contain essentially the same DNA, with a few exceptions; for example, red blood cells do not have a nucleus and contain no DNA. However, although two cells may contain identical DNA, this does not make them identical, because the two cells may have different patterns of ''gene expression''; only some genes will be active in each cell, and the level of activity varies between cells, and this is what makes different cell types different. The "level" of gene expression (for a given gene) is used sometimes to refer to the amount of mRNA made by the cell, and sometimes to refer to the amount of protein produced.
==Flow of information==
There are many interactions that happen between DNA and other molecules to coordinate its functions. When cells divide, the genetic information must be duplicated to produce two complementary copies of DNA in a process called ''[[DNA replication]]''. When a cell uses the information in a gene, the DNA sequence is copied into a complementary single strand of [[RNA]] in a process called ''[[transcription]]''. Of the transcribed sequences, some are used to directly make a matching protein sequence by a process called ''[[translation]]'' (meaning translation from a nucleic acid polymer to an [[amino acid]] polymer). The other transcribed RNA sequences may have regulatory, structural or catalytic roles.  


All humans have essentially the same genes, but have slightly different DNA; on average, the DNA of two individuals differs at about three million bases. These differences are very rarely in the protein-coding sequences of genes, but some affect how particular genes are regulated &mdash; they may affect exactly where in the body a gene is expressed, how intensely it is expressed, or how expression is regulated by other genes or by environmental factors; these slight differences help to make every human being unique. The relative lack of certain enzymes regulated by genes lead to the lack of pigmentation resulting in blue eyes and light skin color. By comparison, the genome of our closest living relative, the [[chimpanzee]], differs from the human genome at about 30 million bases. <ref>Pollard KS ''et al.'' (2006) Forces shaping the fastest evolving regions in the human genome. PLoS Genet 2:[http://genetics.plosjournals.org/perlserv/?request=get-document&doi=10.1371%2Fjournal.pgen.0020168 e168] PMID 17040131</ref>
==== Replication ====
{{further|[[Replication of a circular bacterial chromosome]]}}
[[Image:DNAreplicationFORK.jpg|thumb|400px| '''DNA-replication''' illustrated by the bacterial [[replication fork]]. The helix is unwound and both strands asymetrically replicate simultaneously as they unwind. The ''[[leading strand]]'' replicates continuously from the 3' end (see arrows), with the newest end of the forming strand facing into the replication fork. The ''[[lagging strand]]'' replicates by a series of fragments ([[Okazaki fragments]] placed end-to-end, with the newest ends  facing away from the fork; the Okazaki fragments are later joined together by DNA ligase. During replication, DNA polymerase III proofreads for mismatched bases]]  


===Genomes===
For an organism to grow, its cells must multiply, and this occurs by [[cell division]]: one cell splits to create two new 'daughter' cells. When a cell divides it must make an exact copy of its DNA so that the two daughter cells have the same genetic information as the parent cell. DNA replication requires a complex set of proteins, each dedicated to one of several different tasks needed to replicate this large molecule in an orderly and precise fashion. The double-stranded complementary structure of DNA provides a simple mechanism for this replication. The two strands of DNA are separated by a helicase (an unwinding motor), and then each strand's complementary DNA sequence is recreated by an enzyme called [[DNA polymerase]]. This makes the complementary strand by finding the correct base (through complementary base pairing), and bonding it to the original strand. DNA polymerases can only extend a DNA strand in a 5' to 3' direction, so other mechanisms are needed to copy the asymetrical antiparallel strand of the double helix.<ref>{{cite journal | author = Albà M | title = Replicative DNA polymerases | url=http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=11178285 | journal = Genome Biol | volume = 2 | pages = REVIEWS3002 | year = 2001 | id = PMID 11178285}}</ref> In this way, the base on the old strand dictates which base appears on the new strand, and the cell ends up, after proofreading, with a perfect copy of its DNA.
In eukaryotes, DNA is located mainly in the cell nucleus (there are also small amounts in mitochondria and chloroplasts). In prokaryotes, the DNA is in an irregularly shaped body in the cytoplasm called the [[nucleoid]].<ref>{{cite journal | author = Thanbichler M ''et al.''| title = The bacterial nucleoid: a highly organized and dynamic structure | journal = J Cell Biochem | volume = 96 | pages = 506–21 | year = 2005 | id = PMID 15988757}}</ref> The DNA is usually in linear chromosomes in eukaryotes, and circular chromosomes in prokaryotes. The [[human genome]] has about three billion base pairs of DNA arranged into 46 chromosomes<ref name=Venter/>, and contains 20-25,000 genes <ref>Human Genome Project Information [http://www.ornl.gov/sci/techresources/Human_Genome/home.shtml]</ref>, the simple [[nematode]] ''[[C elegans]]'' has almost as many genes (more than 19,000)<ref>The C. elegans Sequencing Consortium (1998)Genome Sequence of the Nematode C. elegans: A Platform for Investigating Biology. Science
 
282: 2012-8
Further capacity for DNA replication with substantial rearrangement is provided by mechanisms for DNA movement, inversion, and duplication, illustrated by various [[Mobile DNA|mobile DNA]]s such as [[transposons]] and [[proviruses]] (which has major implications for understanding mechanisms of [[molecular evolution]]).
[http://www.sciencemag.org/cgi/content/abstract/282/5396/2012?maxtoshow=&HITS=10&hits=10&RESULTFORMAT=&searchid=1&FIRSTINDEX=0&volume=282&firstpage=2012&resourcetype=HWCIT]</ref>.
 
==== Helicases ====
[[Helicase]]s are a type of '[[molecular active unwinding motor]]'<ref>http://www.news.cornell.edu/stories/July07/helicases.kr.html</ref>used to break hydrogen bonds between bases and unwind the DNA double helix into single strands.<ref>{{cite journal | author = Tuteja N, Tuteja R | title = Unraveling DNA helicases. Motif, structure, mechanism and function | url=http://www.blackwell-synergy.com/links/doi/10.1111%2Fj.1432-1033.2004.04094.x | journal = Eur J Biochem | volume = 271 | pages = 1849–63 | year = 2004 | id = PMID 15128295}}</ref> Helicases are essential for most processes where enzymes need to access the DNA bases. They use the chemical energy in [[nucleoside triphosphate]]s (predominantly [[Adenosine triphosphate|ATP]])


In many species, only a small fraction of the genome encodes protein: only about 1.5% of the human genome consists of protein-coding exons, while over 50% consists of non-coding [[repeated sequence (DNA)|repetitive sequences]].<ref>{{cite journal | author = Wolfsberg T ''et al.''| title = Guide to the draft human genome | journal = Nature | volume = 409 | pages = 824-6 | year = 2001 | id = PMID 11236998}}</ref> While most of the non-coding elements in human DNA were once considered "junk DNA" with no known function, recent studies suggest a variety of roles for these regions, such as RNA silencing<ref name=Volpe>{{cite journal | author = Volpe, TA "et al." | title = Regulation of heterochromatic silencing and histone H3 lysine-9 methylation by RNAi | journal = Science | volume = 297 | pages = 1833-1837 | year = 2002}}</ref> or gene swapping by transposable elements.<ref> name=Biemont>{{cite journal | author = Biemont, C and Vieira, C | title = Genetics: Junk DNA as an evolutionary force | journal = Nature | volume = 443 | pages = 521-524 | year = 2006}}</ref>
The single-stranded DNA exposed by the activity of the helicase enzyme is quickly bound by single-strand DNA binding proteins. In humans, replication protein A is the best-characterised member of this family, and is essential for most processes where the double helix is separated (including DNA replication, recombination and DNA repair).<ref>{{cite journal | author = Iftode C ''et al.''| title = Replication protein A (RPA): the eukaryotic SSB | journal = Crit Rev Biochem Mol Biol | volume = 34 | pages = 141-80 | year = 1999 | id = PMID 10473346}}</ref> These proteins seem to stabilize single-stranded DNA and protect it from forming [[stem loop]]s or being degraded by [[nuclease]]s.


Some other vertebrates, including the puffer fish ''[[Fugu]]'' have very much more compact genomes, and (for multicellular organisms) there seems to be no consistent relationship between the size of the genome and the complexity of the organism <ref> See Sydney Brennar's Nobel lecture (2002) [http://nobelprize.org/nobel_prizes/medicine/laureates/2002/brenner-lecture.pdf]</ref>. Some non-coding DNA sequences are now known to have a structural role in chromosomes. In particular, [[telomere]]s and [[centromere]]s contain few genes, but are important for the function and stability of chromosomes.<ref name=wright>{{cite journal | author = Wright W ''et al.''| title = Normal human chromosomes have long, G-rich telomeric overhangs at one end | url=http://www.genesdev.org/cgi/content/full/11/21/2801#B34 | journal = Genes Dev | volume = 11 | pages = 2801-9 | year = 1997 | id = PMID 9353250}}</ref><ref>{{cite journal | author = Pidoux A, Allshire R | title = The role of heterochromatin in centromere function | url=http://www.journals.royalsoc.ac.uk/media/804t6y8vmh5utlb6ua5y/contributions/p/x/7/a/px7ahm740dq5ueuk.pdf | journal = Philos Trans R Soc Lond B | volume = 360 | pages = 569-79 | year = 2005 | id = PMID 15905142}}</ref> An abundant form of non-coding DNA in humans are [[pseudogene]]s, which are copies of genes that have been disabled by mutation;<ref>{{cite journal | author = Harrison P ''et al.'' | title = Molecular fossils in the human genome: identification and analysis of the pseudogenes in chromosomes 21 and 22 | url=http://www.genome.org/cgi/content/full/12/2/272 | journal = Genome Res | volume = 12 | pages = 272-80 | year = 2002 | id = PMID 11827946}}</ref> these are usually just molecular 'fossils', but they can provide the raw genetic material for new genes.<ref>{{cite journal | author = Harrison P, Gerstein M | title = Studying genomes through the aeons: protein families, pseudogenes and proteome evolution | journal = J Mol Biol | volume = 318 |pages = 1155-74 | year = 2002 | id = PMID 12083509}}</ref>
====Topoisomerases ====  
[[Image:Topisomerasesv2.jpg|thumb|250px|Topoisomerase activities illustrated with  on covalently closed circular DNA. Topisomerases can form supercoils in DNA, and can interconvert covalently closed circular DNA and their catenated forms.]]


A recent challenge to the long-standing view that the human genome consists of relatively few genes along with a vast amount of "[[junk DNA]]" comes from the ENCyclopedia Of DNA Elements ([[ENCODE]]) consortium.<ref>{{cite journal | author = Weinstock GM | title = ENCODE: More genomic empowerment | journal = Genome Research| volume = 17 | pages = 667-668 | year = 2007 | id = PMID 17567987}}</ref><ref name=ENCODE>{{cite journal | author = ENCODE Project Consortium | title = Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project| journal = Nature| volume = 447 | pages = 799-816 | year = 2007 | id = PMID 17571346}}</ref> Their survey of the human genome shows that most of the DNA is transcribed into molecules of [[RNA]]. This broad pattern of transcription was unexpected, but whether these transcribed (but not translated) elements have any biological function is not yet clear.<ref name=ENCODE/>
DNA can be 'twisted' in a process called [[DNA supercoil]]ing. In its "relaxed" state, a DNA strand usually circles the axis of the double helix once every 10.4 base pairs, but if the DNA is twisted, the strands become more tightly or more loosely wound. If the DNA is twisted in the direction of the helix (positive supercoiling), the bases are held more tightly together. If they are twisted in the opposite direction (negative supercoiling) the bases come apart more easily. [[Topoisomerase]]s have both nuclease and ligase activity, and they can change the amount of [[DNA supercoil|supercoiling]] in DNA. Most DNA has slight negative supercoiling that is introduced by [[topoisomerase]]s.
 
These enzymes are needed to relieve the twisting stresses introduced into DNA strands during processes such as [[transcription (genetics)|transcription]] and [[DNA replication]].<ref name=Wang>{{cite journal | author = Wang J | title = Cellular roles of DNA topoisomerases: a molecular perspective | journal = Nat Rev Mol Cell Biol | volume = 3 |pages = 430–40 | year = 2002 | id = PMID 12042765}}</ref>When a section of the double helix is being unwound, the remaining sections can be tangled.  Type 1 toppoisomerases work by cutting the DNA helix and allowing one section to rotate; the enzyme then seals the DNA break.  Type 11  cuts one DNA helix and then pass a second strand of DNA through this break, before rejoining the helix.<ref>{{cite journal | author = Schoeffler A, Berger J | title = Recent advances in understanding structure-function relationships in the type II topoisomerase mechanism | journal = Biochem Soc Trans | volume = 33 | pages = 1465–70 | year = 2005 | id = PMID 16246147}}</ref><ref>{{cite journal | author = Champoux J | title = DNA topoisomerases: structure, function, and mechanism | journal = Ann Rev Biochem | volume = 70 | issue = | pages = 369–413 | year = | url=http://www.fhcrc.org/science/labs/stoddard/MCB_542/champoux_review_2001.pdf | id = PMID 11395412}}</ref>


===Regulation of gene expression===
==== Polymerases ====
How genes are regulated &mdash; how they are turned on or off &mdash; is an important topic in modern biology, and research continually yields surprising insights into how [[phenotypic]] traits and biological [[adaptations]] are determined.
The replicative polymerases are required for the faithful replication of the genetic material and they perform this role by attaching the appropriate nucleotide to the nascent strand to match the template strand. <ref>http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=150442</ref>Accuracy is very important for this, so many polymerases have a [[Proofreading#Proofreading in biology|proofreading]] activity which can recognize the occasional mistakes that can occur during synthesis. These enzymes detect the lack of base pairing between mismatched nucleotides, and if a mismatch is detected, a 3′ to 5′ [[exonuclease]] activity is activated and the incorrect base is removed.<ref>{{cite journal | author = Hubscher U ''et al.'' | title = Eukaryotic DNA polymerases | journal = Annu Rev Biochem | volume = 71 |pages = 133–63 | year = | id = PMID 12045093}}</ref> In most organisms, DNA polymerases function in a large complex called the [[replisome]].


In the 1950's, investigations of the bacterium ''[[Escherichia coli]]'' led to the recognition that the region upstream of a transcribed region provides a place for the enzyme [[RNA polymerase]] to attach to DNA and start transcribing RNA in the 5' to 3' direction of the nucleic acid chain. The site at which this occurs came to be called the ''[[promoter (genetics)|promoter]]''. Other regulatory proteins (such as ''repressors)'' influence transcription by binding to a region near to or overlapping the promoter, called the ''[[operator]]''. In the early years of modern genetics, emphasis was given to transcriptional regulation as an important and common means of modulating gene expression, but today we realize that there are a wide range of mechanisms by which the expression of mRNA and proteins can be modulated by both external and internal signals in cells.
Polymerases  synthesise polynucleotides from [[nucleoside triphosphate]]s. They add nucleotides onto the 3′ [[hydroxyl|hydroxyl group]] of the previous nucleotide in the DNA strand, so all polymerases work in a 5′ to 3′ direction. In the [[active site]] of these enzymes, the nucleoside triphosphate substrate base-pairs to a single-stranded polynucleotide template: this allows polymerases to synthesise the complementary strand of this template accurately.  


==Physical and chemical properties==
RNA-dependent DNA polymerases copy the sequence of an RNA strand into DNA. One example is [[reverse transcriptase]], which is a viral enzyme involved in the infection of cells by [[retrovirus]]es; another example is [[telomerase]], which is required for the replication of [[telomere]]s. Telomerase is an unusual polymerase because it contains its own RNA template as part of its structure.<ref>{{cite journal |author=Nugent C, Lundblad V |title=The telomerase reverse transcriptase: components and regulation | url=http://www.genesdev.org/cgi/content/full/12/8/1073 | journal=Genes Dev |volume=12 | pages=1073&ndash;85 |year=1998 |pmid=9553037}}</ref>
[[Image:DNA_chemical_structure.png|right|thumb|280px|The two strands of DNA are held together by hydrogen bonds between bases. The sugars in the backbone are shown in light blue.]]


DNA is a long chain of repeating units called ''nucleotides'' (a nucleotide is a base linked to a sugar and one or more phosphate groups)<ref name=Alberts>{{cite book | last = Alberts| first = Bruce| coauthors = Alexander Johnson, Julian Lewis, Martin Raff, Keith Roberts, and Peter Walters | title = Molecular Biology of the Cell; Fourth Edition | publisher = Garland Science| date = 2002 | location = New York and London | url = http://www.ncbi.nlm.nih.gov/books/bv.fcgi?call=bv.View..ShowTOC&rid=mboc4.TOC&depth=2 | id = ISBN 0-8153-3218-1}}</ref> The DNA chain is 22-26 Å wide (2.2-2.6nm)<ref>{{cite journal | author = Mandelkern M ''et al.'' | title = The dimensions of DNA in solution | journal = J Mol Biol | volume = 152 | pages = 153-61 | year = 1981 | id = PMID 7338906}}</ref> The nucleotides are very small (just 3.3Å long), but DNA can contain millions of them: the DNA in the largest human chromosome (Chromosome 1) has 220 million base pairs.<ref>{{cite journal | author = Gregory S ''et al.'' | title = The DNA sequence and biological annotation of human chromosome 1 | journal = Nature | volume = 441 | pages = 315-21 | year = 2006 | id = PMID 16710414}}</ref>
==== Transcription ====
Transcription is carried out by a [[RNA polymerase]] that copies a DNA sequence into RNA. The enzyme binds to a promoter and separates the DNA strands. It then copies the gene sequence into a mRNA transcript until it reaches a region of DNA called the ''[[terminator (genetics)|terminator]]'', where it halts and detaches from the DNA. This complementary copy is then decoded by a [[ribosome]] that reads the RNA sequence by base-pairing the mRNA to a specific [[aminoacyl-tRNA]]; an amino acid carried by a [[transfer RNA]] (tRNA). There is one start codon (AUG, which also encodes for [[methionine]]) and three 'stop' or 'nonsense' codons (UAA, UGA and UAG) that signify the end of the coding region.


In living organisms, DNA does not usually exist as a single molecule, but as a tightly-associated pair of molecules.<ref name=Watson>{{cite journal | author = Watson J, Crick F | title = Molecular structure of nucleic acids; a structure for deoxyribose nucleic acid | url=http://profiles.nlm.nih.gov/SC/B/B/Y/W/_/scbbyw.pdf | journal = Nature | volume = 171 | pages = 737-8 | year = 1953 | id = PMID 13054692}}</ref><ref name=berg>Berg J ''et al.'' (2002) ''Biochemistry.'' WH Freeman and Co. ISBN 0-7167-4955-6</ref> These two long strands are entwined in the shape of a [[helix|double helix]]. DNA can thus be thought of as an anti-parallel double helix. The nucleotide repeats contain both the backbone of the molecule, which holds the chain together, and a base, which interacts with the other DNA strand. The double helix is held together by [[hydrogen bond]]s between the bases attached to the two strands. If many nucleotides are linked together, as in DNA, the [[polymer]] is referred to as a [[polynucleotide]].<ref name=IUPAC>[http://www.chem.qmul.ac.uk/iupac/misc/naabb.html Abbreviations and Symbols for Nucleic Acids, Polynucleotides and their Constituents] IUPAC-IUB Commission on Biochemical Nomenclature (CBN) Accessed 03 Jan 2006</ref>
The genetic code consists of three-letter 'words' called ''[[codon]]s'' formed from a sequence of three nucleotides. As there are four bases in three-letter combinations, there are 64 possible codons, and these encode the twenty [[list of standard amino acids|standard amino acids]]. For example, the sequences ACU, CAG and UUU in mRNA are translated to threonine, glutamine and phenylalanine, respectively. Many amino acids, have more than one possible codon (for example, ACU and ACA both code for threonine)


The backbone of the DNA strand has alternating phosphate and sugar residues<ref name=Ghosh>{{cite journal | author = Ghosh A, Bansal M | title = A glossary of DNA structures from A to Z | journal = Acta Crystallogr D Biol Crystallogr | volume = 59 | pages = 620-6 | year = 2003 | id = PMID 12657780}}</ref>: the sugar is the [[pentose]] (five carbon) sugar 2-deoxyribose. The sugar molecules are joined together by phosphate groups that form [[phosphodiester bond]]s between the third and fifth carbon atoms in the sugar rings. Because these bonds are asymmetric, a strand of DNA has a 'direction'. In a double helix, the direction of the nucleotides in one strand is opposite to that in the other strand. This arrangement of DNA strands is called ''antiparallel''. The asymmetric ends of a strand of DNA bases are referred to as the [[5' end|5']] (''five prime'') and [[3' end|3']] (''three prime'') ends. One of the major differences between DNA and RNA is the sugar: 2-deoxyribose is replaced by [[ribose]] in RNA.<ref name=berg/>
RNA polymerase II, which transcribes most of the genes in the human genome, operates as part of a large protein complex with multiple regulatory and accessory subunits.<ref>{{cite journal | author = Martinez E | title = Multi-protein complexes in eukaryotic gene transcription | journal = Plant Mol Biol | volume = 50 | pages = 925–47 | year = 2002 | id = PMID 12516863}}</ref>


The four bases in DNA are adenine (A), cytosine (C), guanine (G) and thymine (T), and these bases are attached to the sugar/phosphate to form the complete nucleotide. Adenine and guanine are fused five- and six-membered [[heterocyclic compound]]s called [[purine]]s, while cytosine and thymine are six-membered rings called [[pyrimidine]]s.<ref name=IUPAC/> A fifth pyrimidine base, [[uracil]] (U), replaces thymine in RNA. Uracil is normally only found in DNA as a breakdown product of cytosine, but [[phage|bacterial viruses]] contain uracil in their DNA.<ref name="nature1963-takahashi">{{cite journal | author=Takahashi I, Marmur J | title=Replacement of thymidylic acid by deoxyuridylic acid in the deoxyribonucleic acid of a transducing phage for Bacillus subtilis | journal=Nature | year=1963 | pages=794-5 | volume=197 | id=PMID 13980287}}</ref> In contrast, following synthesis of certain RNA molecules, many uracils are converted to thymines. This occurs mostly on structural and enzymatic RNAs like tRNAs and [[ribosomal RNA]].<ref>{{cite journal |author=Agris P |title=Decoding the genome: a modified view |
==== Translation ====
url=http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=14715921 |journal=Nucleic Acids Res |volume=32 |pages=223 – 38 |year=2004 |pmid=14715921}}</ref>
After a gene that encodes a protein is transcribed to a messenger RNA (mRNA), the code is delivered to an RNA/protein complex, an multienzyme, called a ribosome. The code is transferred to the ribosome by tRNA, which then translates the genetic code in a step by step process and assembles a string of amino acids one by one until the a stop codon is reached at which time the completed polypeptide is released into the cytoplasm. Several ribosomes may move along the mRNA simultaneously.


The double helix is a right-handed spiral. As the DNA strands wind around each other, gaps between the two phosphate backbones reveal the sides of the bases inside (see animation). Two of these grooves twist around the surface of the double helix: the major groove is 22&nbsp;Å wide and the minor groove is 12&nbsp;Å wide.<ref>{{cite journal | author = Wing R ''et al.''| title = Crystal structure analysis of a complete turn of B-DNA | journal = Nature | volume = 287 | pages = 755 – 8 | year = 1980 | id = PMID 7432492}}</ref> The edges of the bases are more accessible in the major groove, so proteins like [[transcription factor]]s that can bind to specific sequences in double-stranded DNA usually make contacts to the sides of the bases exposed in the major groove.<ref name=Pabo>{{cite journal | author = Pabo C, Sauer R | title = Protein-DNA recognition | journal = Ann Rev Biochem | volume = 53 |pages = 293-321 | year = | id = PMID 6236744}}</ref> For many DNA: protein complexes, up to one-half of the contacts involve the DNA phosphate groups, and thus many DNA binding proteins have more positive amino acids (lysine and arginine) than usual.
==== Sense and antisense ====
When the double strand is separated, two antiparallel strands exist. The DNA sequence that is translated into protein is a "sense" sequence. The sequence on the opposite strand is the "antisense" sequence. Sense and antisense sequences co-exist on the same strand of DNA; in both prokaryotes and eukaryotes, antisense sequences are transcribed<ref>{{cite journal | author = Hüttenhofer A ''et al.''| title = Non-coding RNAs: hope or hype? | journal = Trends Genet | volume = 21 |pages = 289-97 | year = 2005 | id = PMID 15851066}}</ref>, and antisense RNAs might be involved in regulating gene expression.<ref>{{cite journal | author = Munroe S | title = Diversity of antisense regulation in eukaryotes: multiple mechanisms, emerging patterns | journal = J Cell Biochem | volume = 93 | pages = 664-71 | year = 2004 | id = PMID 15389973}}</ref>. (''See [[Micro RNA]], [[RNA interference]], [[sRNA]]''.)


===Base pairing===
== Nature of genes==
Each type of base on one strand of DNA forms a bond with just one type of base on the other strand, called 'complementary [[base pair]]ing'. Purines form hydrogen bonds to pyrimidines; for example, A bonds only to T, and C bonds only to G. This arrangement of two nucleotides joined together across the double helix is called a ''base pair''. In a double helix, the two strands are also held together by [[hydrophobic effect]]s and by a variation of [[pi stacking]].<ref>{{cite journal | author = Ponnuswamy P, Gromiha M | title = On the conformational stability of oligonucleotide duplexes and tRNA molecules | journal = J Theor Biol | volume = 169 |  pages = 419-32 | year = 1994 | id = PMID 7526075}}</ref> Hydrogen bonds can be broken and rejoined quite easily, so the two strands of DNA in a double helix can be pulled apart like a zipper, either by  mechanical force or by high temperatures.<ref>{{cite journal | author = Clausen-Schaumann H ''et al.'' | title = Mechanical stability of single DNA molecules | url=http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=1300792&blobtype=pdf | journal = Biophys J | volume = 78 |  pages = 1997-2007 | year = 2000 | id = PMID 10733978}}</ref> Becauseof this complementarity, the information in the double-stranded sequence of a DNA helix is duplicated on each strand, and this is vital in DNA replication. The reversible and specific interaction between complementary base pairs is critical for all the functions of DNA in living organisms.<ref name=Alberts/>  
DNA contains the genetic information that is the basis for living functions including growth, reproduction and evolution. This information is held in segments of the DNA called ''genes'' that may span in size from dozens of DNA base-pairs to many thousands of base-pairs. All humans have essentially the same genes, but have slightly different DNA; on average, the DNA of two individuals differs at about three million bases. These differences are rarely in the protein-coding sequences of genes, but can affect how particular genes are regulated &mdash;, exactly where in the body a gene is expressed, how intensely it is expressed, or how expression is regulated by other genes or by environmental factors. These slight differences help to make every human being unique. By comparison, the genome of our closest living relative, the [[chimpanzee]], differs from the human genome by about 30 million bases. <ref>Pollard KS ''et al.'' (2006) Forces shaping the fastest evolving regions in the human genome. PLoS Genet 2:[http://genetics.plosjournals.org/perlserv/?request=get-document&doi=10.1371%2Fjournal.pgen.0020168 e168] PMID 17040131</ref>


The two types of base pairs form different numbers of hydrogen bonds; AT forms two hydrogen bonds, and GC forms three, so the GC base-pair is stronger than the AT pair. Thus, long DNA helices with a high GC content have strongly interacting strands, while short helices with high AT content have weakly interacting strands.<ref>{{cite journal | author = Chalikian T ''et al.''| title = A more unified picture for the thermodynamics of nucleic acid duplex melting: a characterization by calorimetric and volumetric techniques | url=http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=22151&blobtype=pdf | journal = Proc Natl Acad Sci USA | volume = 96 | pages = 7853-8 | year = 1999 | id = PMID 10393911}}</ref> Parts of the DNA double helix that need to separate easily tend to have a high AT content, making the strands easier to pull apart.<ref>{{cite journal | author = deHaseth P, Helmann J | title = Open complex formation by Escherichia coli RNA polymerase: the mechanism of polymerase-induced strand separation of double helical DNA | journal = Mol Microbiol | volume = 16 | pages = 817-24 | year = 1995 | id = PMID 7476180}}</ref> The strength of this interaction can be measured by finding the temperature required to break the hydrogen bonds (their '[[melting temperature]]'). When all the base pairs in a DNA double helix melt, the strands separate, leaving two single-stranded molecules in solution. Because base-pairing causes changes in the UV-visible spectrum of the bases, DNA melting can be monitored by observing the hypochronicity (or loss thereof) as a function of temperature. These molecules have no single shape, but some conformations are more stable than others.
DNA usually occurs as several large, linear [[chromosome]]s, each of which may contain hundreds or thousands of genes in [[eukaryotes]]. The complete set of chromosomes in a cell makes up its [[genome]]; the [[human genome]] has about three billion base pairs of DNA arranged into 46 chromosomes <ref name=Venter>{{cite journal | author = Venter J ''et al.'' | title = The sequence of the human genome | journal = Science | volume = 291 | pages = 1304–51 | year = 2001 | id = PMID 11181995}}</ref> and contains about 20,000 genes.<ref name=HGP>Human Genome Project Information [http://www.ornl.gov/sci/techresources/Human_Genome/home.shtml]</ref> [[Prokaryotes]]  generally have a single large circular chromosome, but they often possess other miniature chromosomes called plasmids.  


===Sense and antisense===
====The elusive definition====
A DNA sequence is a "sense" sequence if it is the same as that of a mRNA copy that is translated into protein. The sequence on the opposite strand is the "antisense" sequence. Sense and antisense sequences can co-exist on the same strand of DNA; in both prokaryotes and eukaryotes, antisense sequences are transcribed<ref>{{cite journal | author = Hüttenhofer A ''et al.''| title = Non-coding RNAs: hope or hype? | journal = Trends Genet | volume = 21 |pages = 289-97 | year = 2005 | id = PMID 15851066}}</ref>, and antisense RNAs might be involved in regulating gene expression.<ref>{{cite journal | author = Munroe S | title = Diversity of antisense regulation in eukaryotes: multiple mechanisms, emerging patterns | journal = J Cell Biochem | volume = 93 | pages = 664-71 | year = 2004 | id = PMID 15389973}}</ref>. (''See [[Micro RNA]], [[RNA interference]], [[sRNA]]''.)
Gene comes from a Greek word meaning "to give birth to". Our understanding of the role genes play in cells, has been continually revised throughout the history of genetics. This has led to several definitions of a gene starting from abstract concepts of inheritable "factors" whose composition was unknown. One way to define a gene is simply as a segment of DNA that is transcribed into RNA - that is - ''the gene is a unit of transcription''. This definition encompasses genes for non-coding RNAs, such as [[ribosomal RNA]] ([[rRNA]]) and [[transfer RNA]] ([[tRNA]]), as well as [[messenger RNA]] ([[mRNA]]) which ''is'' used for encoding the sequences of proteins. As defined in this case, a gene then is that whole unit of genetic information which is transcribed and translated into proteins.


Many DNA sequences in prokaryotes and eukaryotes (and more in plasmids and viruses) have overlapping genes which may both occur in the same direction, on the same strand (parallel) or in opposite directions, on opposite strands (antiparallel).<ref>{{cite journal | author = Makalowska I ''et al.''| title = Overlapping genes in vertebrate genomes | journal = Comput Biol Chem | volume = 29 | pages = 1–12 | year = 2005 | url=http://warta.bio.psu.edu/PDF/cbac_2005_29_1.pdf | id = PMID 15680581}}</ref><ref name="johnson">{{cite journal | author = Johnson Z, Chisholm S | title = Properties of overlapping genes are conserved across microbial genomes | journal = Genome Res | volume = 14 | pages = 2268–72 | year = 2004 | url=http://www.genome.org/cgi/content/full/14/11/2268 | id = PMID 15520290}}</ref> In these cases, some DNA sequences encode one protein when read from 5′ to 3′ along one strand, and a different protein when read in the opposite direction (but still from 5′ to 3′) along the other strand. In bacteria, this overlap may be involved in regulating gene transcription,<ref name="johnson" /> while in [[viruses]], overlapping genes increase the information that can be encoded within the small viral genome.<ref>{{cite journal | author = Lamb R, Horvath C | title = Diversity of coding strategies in [[influenza]] viruses | journal = Trends Genet | volume = 7 |  pages = 261–6 | year = 1991 | id = PMID 1771674}}</ref> Another way of reducing genome size is seen in some viruses that contain linear or circular ''single-stranded'' DNA.<ref>{{cite journal | author = Davies J, Stanley J | title = Geminivirus genes and vectors | journal = Trends Genet | volume = 5 | pages = 77–81 | year = 1989 | id = PMID 2660364}}</ref>
A second approach is to define a gene as ''a region of DNA that encodes a single polypeptide''. By this definition, any particular mRNA transcription unit can contain more than one gene, and thus a mRNA can carry regions encoding one or more polypeptides. Such a multi-genic transcription unit is called an [[operon]] and are common in prokaryotic cells.Both these definitions are similar to a "bead on a string" analogy with distinct genes as sequentially ordered units along a chromosome.


===Supercoiling===
A more fuzzy definition considers genes as ''units of biological function''. This definition can include ''cis''-acting sequences of DNA that are not transcribed and flank a coding region.  They act as specific binding sites for a variety of [[transcription factor]] proteins involved with regulating gene expression. Examples of such sequences are [[enhancer]]s, [[promoter]]s and [[operator]]s. In this model the "bead on a string" analogy breaks down since the ''cis''-acting factors from different genes do overlap and this is closer to the reality of gene structure in a chromosome.
DNA can be 'twisted' in a process called [[DNA supercoil]]ing. In its "relaxed" state, a DNA strand usually circles the axis of the double helix once every 10.4 base pairs, but if the DNA is twisted, the strands become more tightly or more loosely wound.<ref>{{cite journal | author = Benham C, Mielke S | title = DNA mechanics | journal = Ann Rev Biomed Eng | volume = 7 | pages = 21–53 | year = | id = PMID 16004565}}</ref> If the DNA is twisted in the direction of the helix (positive supercoiling), and the bases are held more tightly together. If they are twisted in the opposite direction (negative supercoiling) the bases come apart more easily. Most DNA has slight negative supercoiling that is introduced by [[topoisomerase]]s. These enzymes are also needed to relieve the twisting stresses introduced into DNA strands during processes such as [[transcription (genetics)|transcription]] and [[DNA replication]].<ref name=Wang>{{cite journal | author = Wang J | title = Cellular roles of DNA topoisomerases: a molecular perspective | journal = Nat Rev Mol Cell Biol | volume = 3 |pages = 430–40 | year = 2002 | id = PMID 12042765}}</ref>


===Alternative conformations===
Because of these various factors, the exact number of genes in a human organism has not yet been determined.<ref>Insert footnote text here</ref>
The conformation of a DNA molecule depends on its sequence, the amount and direction of supercoiling, chemical modifications of the bases, and also solution conditions, such as the concentration of metal ions.<ref>{{cite journal | author = Basu H ''et al.'' | title = Recognition of Z-RNA and Z-DNA determinants by polyamines in solution: experimental and theoretical studies | journal = J Biomol Struct Dyn | volume = 6 |  pages = 299-309 | year = 1988 | id = PMID 2482766}}</ref> Accordingly, DNA can exist in several possible conformations, but only a few of these ("A-DNA", "B-DNA", and "Z-DNA") are thought to occur naturally. Of these, the "B" form is most common. The A form is a wider right-handed spiral, with a shallow and wide minor groove and a narrower and deeper major groove; this form occurs in dehydrated samples of DNA, while in the cell it may be produced in hybrid pairings of DNA and [[RNA]] strands, as well as in enzyme-DNA complexes.<ref>{{cite journal |author=Lu XJ ''et al.'' |title=A-form conformational motifs in ligand-bound DNA structures |journal=J Mol Biol |volume=300|pages=819-40 |year=2000 |pmid=10891271}}</ref> Segments of DNA where the bases have been modified by [[methylation]] may undergo a larger change in conformation and adopt the Z form. Here, the strands turn about the helical axis in a left-handed spiral, the opposite of the more common B form.<ref>{{cite journal | author = Rothenburg S ''et al.'' | title = DNA methylation and Z-DNA formation as mediators of quantitative differences in the expression of alleles | journal = Immunol Rev | volume = 184 |  pages = 286–98 | year = | id = PMID 12086319}}</ref> These unusual structures can be recognized by specific Z-DNA binding proteins and may be involved in regulating transcription.<ref>{{cite journal |author=Oh D ''et al.'' |title=Z-DNA-binding proteins can act as potent effectors of gene expression ''in vivo'' |url=http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=12486233 |journal=Proc Natl Acad Sci USA |volume=99 |pages=16666-71 |year=2002 |pmid=12486233}}</ref>


===Quadruplex structures===
==== Expression of genes ====
At the ends of the linear chromosomes, specialized regions called [[telomere]]s allow the cell to replicate chromosome ends using the enzyme [[telomerase]].<ref name=Greider>{{cite journal | author = Greider C, Blackburn E | title = Identification of a specific telomere terminal transferase activity in Tetrahymena extracts | journal = Cell | volume = 43 | pages = 405-13 | year = 1985 | id = PMID 3907856}}</ref> Without telomeres, a chromosome would become shorter each time it was replicated. These specialized 'caps' also help to protect the DNA ends from [[exonuclease]]s and stop the [[DNA repair]] systems in the cell from treating them as damage to be corrected. In human cells, telomeres are usually lengths of single-stranded DNA that contain several thousand repeats of a TTAGGG sequence.<ref name=wright/> These sequences may stabilize chromosome ends by forming unusual quadruplex structures. Here, four guanine bases form a flat plate, through[[ hydrogen bonding]], and these plates then stack on top of each other to form a stable quadruplex.<ref name=Burge>{{cite journal | author = Burge S ''et al.'' | title = Quadruplex DNA: sequence, topology and structure | url=http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=17012276 | journal = Nucleic Acids Res | volume = 34 | pages = 5402-15 | year = 2006 | id = PMID 17012276}}</ref> Other structures can also be formed, and the central set of four bases can come from either one folded strand, or several different parallel strands, each contributing one base to the central structure.
How genes are regulated &mdash; how they are turned on or off &mdash; is an important topic in modern biology, and research continually yields surprising insights into how [[phenotypic]] traits and biological [[adaptations]] are determined.


Telomeres also form large loops called '[[telomere loops]]', or '[[T-loops]]'. Here, the single-stranded DNA curls around in a circle stabilized by telomere-binding proteins.<ref>{{cite journal | author = Griffith J ''et al.'' | title = Mammalian telomeres end in a large duplex loop | journal = Cell | volume = 97 |  pages = 503-14 | year = 1999 | id = PMID 10338214}}</ref>
In the 1950's, investigations of the bacterium ''[[Escherichia coli]]'' led to the recognition that the region upstream of a transcribed region provides a place for the enzyme [[RNA polymerase]] to attach to DNA and start transcribing RNA in the 5' to 3' direction of the nucleic acid chain. The site at which this occurs came to be called the ''[[promoter (genetics)|promoter]]''. Other regulatory proteins (such as ''repressors)'' influence transcription by binding to a region near to or overlapping the promoter, called the ''[[operator]]''. In the early years of modern genetics, emphasis was given to transcriptional regulation as an important and common means of modulating gene expression, but today we realize that there are a wide range of mechanisms by which the expression of mRNA and proteins can be modulated in cells.


==Chemical modifications==
Many DNA sequences in prokaryotes and eukaryotes (and more in plasmids and viruses) have overlapping genes which may both occur in the same direction, on the same strand (parallel) or in opposite directions, on opposite strands (antiparallel).<ref>{{cite journal | author = Makalowska I ''et al.''| title = Overlapping genes in vertebrate genomes | journal = Comput Biol Chem | volume = 29 | pages = 1–12 | year = 2005 | url=http://warta.bio.psu.edu/PDF/cbac_2005_29_1.pdf | id = PMID 15680581}}</ref><ref name="johnson">{{cite journal | author = Johnson Z, Chisholm S | title = Properties of overlapping genes are conserved across microbial genomes | journal = Genome Res | volume = 14 | pages = 2268–72 | year = 2004 | url=http://www.genome.org/cgi/content/full/14/11/2268 | id = PMID 15520290}}</ref> In these cases, some DNA sequences encode one protein when read from 5′ to 3′ along one strand, and a different protein when read in the opposite direction (but still from 5′ to 3′) along the other strand. In bacteria, this overlap may be involved in regulating gene transcription,<ref name="johnson" /> while in [[viruses]], overlapping genes increase the information that can be encoded within the small viral genome.<ref>{{cite journal | author = Lamb R, Horvath C | title = Diversity of coding strategies in [[influenza]] viruses | journal = Trends Genet | volume = 7 | pages = 261–6 | year = 1991 | id = PMID 1771674}}</ref> Another way of reducing genome size is seen in some viruses that contain linear or circular ''single-stranded'' DNA.<ref>{{cite journal | author = Davies J, Stanley J | title = Geminivirus genes and vectors | journal = Trends Genet | volume = 5 | pages = 77–81 | year = 1989 | id = PMID 2660364}}</ref>
===DNA methylation===
The expression of genes is influenced by the [[chromatin]] structure of a chromosome, and regions of [[heterochromatin]] (with little or no gene expression) correlate with the [[methylation]] of [[cytosine]].<ref> For example, cytosine methylation, to produce [[5-Methylcytosine|5-methylcytosine]], is important for [[X-inactivation|X-chromosome inactivation]]. {{cite journal | author = Klose R, Bird A | title = Genomic DNA methylation: the mark and its mediators | journal = Trends Biochem Sci | volume = 31 | pages = 89–97 | year = 2006 | id = PMID 16403636}}</ref> These structural changes to the DNA are one type of [[epigenetic]] change that can alter chromatin structure, and they are inheritable. ''Epigenetics'' refers to features of organisms that are stable over successive rounds of cell division but which do not involve changes in the underlying DNA sequence<ref>{{cite journal| title=Perceptions of epigenetics| author=Adrian Bird| journal=Nature| volume=447| pages=396-398| year=2007}} PMID 17522671</ref>. Epigenetic changes are important in [[morphogenesis|cellular differentiation]], allowing cells to maintain different characteristics despite containing the same genomic material. Some epigenetic features can be inherited from one generation to the next.<ref>{{cite journal| title=Paramutation: From Maize to Mice| author=V.L. Chandler| journal=Cell| volume=128| pages=641-645| year=2007}}</ref>


The level of methylation varies between organisms; the nematode ''C. elegans'' lacks any cytosine methylation, while up to 1% of the DNA of vertebrates contains 5-methylcytosine.<ref>{{cite journal | author = Bird A | title = DNA methylation patterns and epigenetic memory | journal = Genes Dev | volume = 16 | pages = 6–21 | year = 2002 | id = PMID 11782440}}</ref> Despite the biological importance of 5-methylcytosine, it is susceptible to spontaneous [[deamination]], and methylated cytosines are therefore [[mutation]] 'hotspots'.<ref>{{cite journal | author = Walsh C, Xu G | title = Cytosine methylation and DNA repair | journal = Curr Top Microbiol Immunol | volume = 301 | pages = 283–315 | year = | id = PMID 16570853}}</ref> Other base modifications include adenine methylation in bacteria and the [[glycosylation]] of uracil to produce the "J-base" in [[kinetoplastid]]s.<ref>{{cite journal | author = Ratel D ''et al.''| title = N6-methyladenine: the other methylated base of DNA | journal = Bioessays | volume = 28 | pages = 309–15 | year = 2006 | id = PMID 16479578}}</ref><ref>{{cite journal | author = Gommers-Ampt J ''et al.''| title = beta-D-glucosyl-hydroxymethyluracil: a novel modified base present in the DNA of the parasitic protozoan T. brucei | journal = Cell | volume = 75 | pages = 1129–36 | year = 1993 | id = PMID 8261512}}</ref>
==== Trans acting proteins ====
All of the functions of DNA depend on its interactions with proteins. Some of these interactions are non-specific, others are specific in that the protein can only bind to a particular DNA sequence. Some enzymes can also bind to DNA and of these, the polymerases that copy the DNA base sequence in transcription and DNA replication are particularly important.


===Mutations===
Other proteins bind to particular DNA sequences. The most intensively studied of these are the [[transcription factors]]. Each of these proteins binds to a particular set of DNA sequences and thereby activates or inhibits the transcription of genes with these sequences close to their [[promoter]]s. Transcription factors do this in two ways. Some can bind the RNA polymerase responsible for transcription, either directly or through other mediator proteins; this locates the polymerase at the promoter and allows it to begin transcription.<ref>{{cite journal | author = Myers L, Kornberg R | title = Mediator of transcriptional regulation | journal = Ann Rev Biochem | volume = 69 | issue = | pages = 729-49 | year = | id = PMID 10966474}}</ref> Other transcription factors can bind enzymes that modify the histones at the promoter, this will change the accessibility of the DNA template to the polymerase.<ref>{{cite journal | author = Spiegelman B, Heinrich R | title = Biological control through regulated transcriptional coactivators | journal = Cell | volume = 119 |  pages = 157-67 | year = 2004 | id = PMID 15479634}}</ref>
DNA can be damaged by many different agents. [[Mutagen]]s are agents which can produce genetic [[mutation]]s - these are alterations of one DNA base to another base. Examples of mutagens include [[oxidizing agent]]s, [[alkylating agent]]s and high-energy [[electromagnetic radiation]] such as [[ultraviolet light]] and [[x-rays]]. ''Lesions'' of DNA, in which residues are changed to a structure that is not a normal feature of DNA, are different from mutations. However, damaged DNA can give rise to mutations, and indeed, some DNA repair processes are ''error prone'' and thus themselves generate mutations.


Ultraviolet radiation damages DNA mostly by producing [[thymine dimer]]s.<ref>{{cite journal | author = Douki T ''et al.'' | title = Bipyrimidine photoproducts rather than oxidative lesions are the main type of DNA damage involved in the genotoxic effect of solar ultraviolet radiation | journal = Biochemistry | volume = 42 |  pages = 9221-6 | year = 2003 | id = PMID 12885257}}</ref> Oxidants such as [[free radical]]s or [[hydrogen peroxide]] can cause several forms of damage, including base modifications (particularly of guanosine) as well as double-strand breaks.<ref>{{cite journal | author = Cadet J ''et al.'' | title = Hydroxyl radicals and DNA base damage | journal = Mutat Res | volume = 424 | issue = 1-2 | pages = 9-21 | year = 1999 | id = PMID 10064846}}</ref> It has been estimated that, in each human cell, about 500 bases suffer oxidative damage every day.<ref>{{cite journal | author = Shigenaga M ''et al.'' | title = Urinary 8-hydroxy-2'-deoxyguanosine as a biological marker of ''in vivo'' oxidative DNA damage | url=http://www.pnas.org/cgi/reprint/86/24/9697 | journal = Proc Natl Acad Sci USA | volume = 86 | pages = 9697-701 | year = 1989 | id = PMID 2602371}}</ref><ref>{{cite journal | author = Cathcart R ''et al.'' | title = Thymine glycol and thymidine glycol in human and rat urine: a possible assay for oxidative DNA damage | url=http://www.pnas.org/cgi/reprint/81/18/5633.pdf | journal = Proc Natl Acad Sci USA | volume = 81 | pages = 5633-7 | year = 1984 | id = PMID 6592579}}</ref> Of these lesions, the most damaging are double-strand breaks, as they can produce [[point mutation]]s, insertions and deletions from the DNA sequence, as well as [[chromosomal translocation]]s.<ref>{{cite journal | author = Valerie K, Povirk L | title = Regulation and mechanisms of mammalian double-strand break repair | journal = Oncogene | volume = 22 |  pages = 5792-812 | year = 2003 | id = PMID 12947387}}</ref>
These DNA targets can occur throughout an organism's genome, so changes in the activity of one type of transcription factor in a given cell can affect the expression of many genes in that cell.<ref>{{cite journal | author = Li Z ''et al.'' | title = A global transcriptional regulatory role for c-Myc in Burkitt's lymphoma cells | url=http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=12808131 | journal = Proc Natl Acad Sci USA | volume = 100 | pages = 8164-9 | year = 2003 | id = PMID 12808131}}</ref> Consequently, these proteins are often the targets of the [[signal transduction]] processes that mediate responses to environmental changes or cellular differentiation and development. The specificity of transcription factor interactions with DNA arises because the proteins make multiple contacts to the edges of the DNA bases, allowing them to "read" the DNA sequence. Most of these interactions occur in the major groove, where the bases are most accessible.<ref name=Pabo/>


Many mutagens [[intercalation (chemistry)|intercalate]] into the space between two adjacent base pairs. These are mostly polycyclic, [[aromatic]], and planar molecules, and include [[ethidium]], [[proflavin]], [[daunomycin]], [[doxorubicin]] and [[thalidomide]]. For an intercalator to fit between base pairs, the bases must separate, distorting the DNA strand by unwinding of the double helix. These structural modifications inhibit transcription and replication processes, causing both toxicity and mutations. As a result, DNA intercalators are often [[carcinogen]]s. Nevertheless, because they can inhibit DNA transcription and replication, they are also used in [[chemotherapy]] to inhibit DNA-replication in rapidly-growing [[cancer]] cells.<ref name=brana>{{cite journal | author = Braña M ''et al.'' | title = Intercalators as anticancer drugs | journal = Curr Pharm Des | volume = 7 |  pages = 1745-80 | year = 2001 | id = PMID 11562309}}</ref>
==The chromosome: DNA's home ==
Nuclear DNA is organized and stored in compacted form into [[chromosome]]s inside the nucleus of the cell. At conception, the male sperm and female ovum contribute 23 chromosomes each, for a total of 46 chromosomes in the fertilized embryo. Mitochondria  have their own DNA which originates in the female egg as a complete double strand.


==Interactions with proteins==
DNA is an enormously long, unbranched linear polymer containing many millions of nucleotides the order of which provides the genetic information. For example an average cell has DNA with about 3X10<sup>9</sup> nucleosides. If each nucleotide were a letter on the page of a large book,they would occupy a million pages. If DNA were stretched out it would measure about 5 cm. but it must be contained in a nucleus measuring 5X10<sup>-4</sup> cm in diameter. To achieve the necessary compactness as well as maintain accessibility, DNA is folded in many ways. The folding is assisted by proteins called histones, their sum is known as chromatin. The nucleosome is the first order of folding, appearing as beads on a string under magnification. In this case the DNA wraps around a histone core shaped like a cylinder. The cylinders are then packed together as groups. The groups are then looped. The folding is necessary for maximum compactness and for accessibility of transcription processes.<ref>Insert footnote text here</ref>
All of the functions of DNA depend on its interactions with proteins. some of these interactions are non-specific, others are specific in that the protein can only bind to a particular DNA sequence. Some enzymes can also bind to DNA and of these, the polymerases that copy the DNA base sequence in transcription and DNA replication are particularly important.


===DNA-binding proteins===
==== Histones ====
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<div style="border: none; width:260px;"><div class="thumbcaption">Interaction of DNA with [[histone]]s (shown in white, top). These proteins' basic amino acids (below left, blue) bind to the acidic phosphate groups on DNA (below right, red).</div></div></div>
<div style="border: none; width:260px;"><div class="thumbcaption">Interaction of DNA with [[histone]]s (shown in white, top). These proteins' basic amino acids (below left, blue) bind to the acidic phosphate groups on DNA (below right, red).</div></div></div>


Within chromosomes, DNA is held in complexes between DNA and structural proteins, forming a compact structure called [[chromatin]]. In eukaryotes, this structure involves DNA binding to small basic proteins called [[histone]]s, while in prokaryotes many types of proteins are involved.<ref>{{cite journal | author = Sandman K ''et al.'' | title = Diversity of prokaryotic chromosomal proteins and the origin of the nucleosome | journal = Cell Mol Life Sci | volume = 54 |pages = 1350-64 | year = 1998 | id = PMID 9893710}}</ref> The histones form a disk-shaped complex called a [[nucleosome]] which has two complete turns of double-stranded DNA wrapped around it. These interactions are formed through basic residues in the histones making [[ionic bond]]s to the acidic sugar-phosphate backbone of the DNA, and are largely independent of the base sequence.<ref>{{cite journal | author = Luger K ''et al.'' | title = Crystal structure of the nucleosome core particle at 2.8 A resolution | journal = Nature | volume = 389 | pages = 251-60 | year = 1997 | id = PMID 9305837}}</ref> Chemical modifications of these basic amino acid residues include [[methylation]], [[phosphorylation]] and [[acetylation]].<ref>{{cite journal | author = Jenuwein T, Allis C | title = Translating the histone code | journal = Science | volume = 293 | pages = 1074-80 | year = 2001 | id = PMID 11498575}}</ref> These changes alter the strength of the interaction between the DNA and the histones, making the DNA more or less accessible to transcription factors and changing the rate of transcription.<ref>{{cite journal | author = Ito T | title = Nucleosome assembly and remodelling | journal = Curr Top Microbiol Immunol | volume = 274 | pages = 1-22 | year = | id = PMID 12596902}}</ref> Other non-specific DNA-binding proteins found in chromatin include the high-mobility group proteins, which bind preferentially to bent or distorted DNA.<ref>{{cite journal | author = Thomas J | title = HMG1 and 2: architectural DNA-binding proteins | journal = Biochem Soc Trans | volume = 29 | pages = 395-401 | year = 2001 | id = PMID 11497996}}</ref> These proteins are important in bending arrays of nucleosomes and arranging them into more complex chromatin structures.<ref>{{cite journal | author = Grosschedl R ''et al.''| title = HMG domain proteins: architectural elements in the assembly of nucleoprotein structures | journal = Trends Genet | volume = 10 | pages = 94-100 | year = 1994 | id = PMID 8178371}}</ref>
DNA is held within the chromosomes as a complex of DNA and structural proteins called [[histone]]s, forming a compact structure called [[chromatin]]. In adition to the histones are a variety of proteins called non-histone chromosomal proteins.  In prokaryotes many types of proteins are involved.<ref>{{cite journal | author = Sandman K ''et al.'' | title = Diversity of prokaryotic chromosomal proteins and the origin of the nucleosome | journal = Cell Mol Life Sci | volume = 54 |pages = 1350-64 | year = 1998 | id = PMID 9893710}}</ref> The histones form a disk-shaped complex called a [[nucleosome]] which has two complete turns of double-stranded DNA wrapped around it.  
 
These interactions are formed by positively charged amino acid  residues in the histones making [[ionic bond]]s to the acidic sugar-phosphate backbone of the DNA, and thereby are largely independent of the base sequence.<ref>{{cite journal | author = Luger K ''et al.'' | title = Crystal structure of the nucleosome core particle at 2.8 A resolution | journal = Nature | volume = 389 | pages = 251-60 | year = 1997 | id = PMID 9305837}}</ref> Chemical modifications of these basic amino acid residues include [[methylation]], [[phosphorylation]] and [[acetylation]].<ref>{{cite journal | author = Jenuwein T, Allis C | title = Translating the histone code | journal = Science | volume = 293 | pages = 1074-80 | year = 2001 | id = PMID 11498575}}</ref> These changes alter the strength of the interaction between the DNA and the histones, making the DNA more or less accessible to transcription factors and changing the rate of transcription.<ref>{{cite journal | author = Ito T | title = Nucleosome assembly and remodelling | journal = Curr Top Microbiol Immunol | volume = 274 | pages = 1-22 | year = | id = PMID 12596902}}</ref> Other non-specific DNA-binding proteins found in chromatin include the high-mobility group proteins, which bind preferentially to bent or distorted DNA.<ref>{{cite journal | author = Thomas J | title = HMG1 and 2: architectural DNA-binding proteins | journal = Biochem Soc Trans | volume = 29 | pages = 395-401 | year = 2001 | id = PMID 11497996}}</ref> These proteins are important in bending arrays of nucleosomes and arranging them into more complex chromatin structures.<ref>{{cite journal | author = Grosschedl R ''et al.''| title = HMG domain proteins: architectural elements in the assembly of nucleoprotein structures | journal = Trends Genet | volume = 10 | pages = 94-100 | year = 1994 | id = PMID 8178371}}</ref>
 
==== Enabling transcription  ====
Not only does the chromosome compact DNA, it allows for transcription while in the compacted state.
 
== Genomes ==
The human genome has about three billion base pairs of DNA arranged into 46 chromosomes<ref name=Venter/> and contains 25-30,000 genes <ref name=HGP/>; the simple nematode ''C. elegans'' has almost as many genes (more than 19,000)<ref>The C. elegans Sequencing Consortium (1998)Genome Sequence of the Nematode C. elegans: A Platform for Investigating Biology. Science
282: 2012-8
[http://www.sciencemag.org/cgi/content/abstract/282/5396/2012?maxtoshow=&HITS=10&hits=10&RESULTFORMAT=&searchid=1&FIRSTINDEX=0&volume=282&firstpage=2012&resourcetype=HWCIT]</ref>.
In eukaryotes, DNA is located mainly in the cell nucleus (there are also small amounts in mitochondria and chloroplasts). In prokaryotes, the DNA is in an irregularly shaped body in the cytoplasm called the nucleoid.<ref>{{cite journal | author = Thanbichler M ''et al.''| title = The bacterial nucleoid: a highly organized and dynamic structure | journal = J Cell Biochem | volume = 96 | pages = 506–21 | year = 2005 | id = PMID 15988757}}</ref> The DNA is usually in linear chromosomes in eukaryotes, and circular chromosomes in prokaryotes.
 
In many species, only a small fraction of the genome encodes protein: only about 1.5% of the human genome consists of protein-coding exons, while over 50% consists of non-coding [[repeated sequence (DNA)|repetitive sequences]].<ref>{{cite journal | author = Wolfsberg T ''et al.''| title = Guide to the draft human genome | journal = Nature | volume = 409 | pages = 824-6 | year = 2001 | id = PMID 11236998}}</ref> While most of the non-coding elements in human DNA were once considered "junk DNA" with no known function, recent studies suggest a variety of roles for these regions, such as RNA silencing<ref name=Volpe>{{cite journal | author = Volpe, TA "et al." | title = Regulation of heterochromatic silencing and histone H3 lysine-9 methylation by RNAi | journal = Science | volume = 297 | pages = 1833-1837 | year = 2002}}</ref> or gene swapping by transposable elements.<ref name=Biemont>{{cite journal | author = Biemont C, Vieira C | title = Genetics: Junk DNA as an evolutionary force | journal = Nature | volume = 443 | pages = 521-4 | year = 2006}}</ref>
 
Some other vertebrates, including the puffer fish ''Fugu'' have more compact genomes, and (for multicellular organisms) there seems to be no consistent relationship between the size of the genome and the complexity of the organism.<ref> See Sydney Brennar's Nobel lecture (2002) [http://nobelprize.org/nobel_prizes/medicine/laureates/2002/brenner-lecture.pdf]</ref> Some non-coding DNA sequences are now known to have a structural role in chromosomes. In particular, telomeres and centromeres contain few genes, but are important for the function and stability of chromosomes.<ref>{{cite journal | author = Pidoux A, Allshire R | title = The role of heterochromatin in centromere function | url=http://www.journals.royalsoc.ac.uk/media/804t6y8vmh5utlb6ua5y/contributions/p/x/7/a/px7ahm740dq5ueuk.pdf | journal = Philos Trans R Soc Lond B | volume = 360 | pages = 569-79 | year = 2005 | id = PMID 15905142}}</ref> An abundant form of non-coding DNA in humans are pseudogenes, which are copies of genes that have been disabled by mutation;<ref>{{cite journal | author = Harrison P ''et al.'' | title = Molecular fossils in the human genome: identification and analysis of the pseudogenes in chromosomes 21 and 22 | url=http://www.genome.org/cgi/content/full/12/2/272 | journal = Genome Res | volume = 12 | pages = 272-80 | year = 2002 | id = PMID 11827946}}</ref> these are usually just molecular 'fossils', but they can provide the raw genetic material for new genes.<ref>{{cite journal | author = Harrison P, Gerstein M | title = Studying genomes through the aeons: protein families, pseudogenes and proteome evolution | journal = J Mol Biol | volume = 318 |pages = 1155-74 | year = 2002 | id = PMID 12083509}}</ref>
 
A recent challenge to the long-standing view that the human genome consists of relatively few genes along with a vast amount of  "[[junk DNA]]" comes from the ENCyclopedia Of DNA Elements ([[ENCODE]]) consortium.<ref>{{cite journal | author = Weinstock GM | title = ENCODE: More genomic empowerment | journal = Genome Research| volume = 17 | pages = 667-668 | year = 2007 | id = PMID 17567987}}</ref><ref name=ENCODE>{{cite journal | author = ENCODE Project Consortium | title = Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project| journal = Nature| volume = 447 | pages = 799-816 | year = 2007 | id = PMID 17571346}}</ref> Their survey of the human genome shows that most of the DNA is transcribed into molecules of [[RNA]]. This broad pattern of transcription was unexpected, but whether these transcribed (but not translated) elements have any biological function is not yet clear.<ref name=ENCODE/>
 
==The good, the neutral and the ugly==
==== Genetic recombination ====
A DNA helix does not usually interact with other segments of DNA, and in human cells the different chromosomes even occupy different regions of the nucleus (called "chromosome territories").<ref>{{cite journal | author = Cremer T, Cremer C | title = Chromosome territories, nuclear architecture and gene regulation in mammalian cells | journal = Nat Rev Genet | volume = 2 |  pages = 292-301 | year = 2001 | id = PMID 11283701}}</ref> This physical separation of chromosomes is important for the ability of DNA to function as a stable repository for information, as one of the few times chromosomes interact is when they [[genetic recombination|recombine]].
 
Recombination is when two DNA helices break, swap a section and then rejoin. In eukaryotes, this usually occurs during [[meiosis]], when two [[chromatid]]s are paired together in the center of the cell. This allows chromosomes to exchange genetic information and produces new combinations of genes.<ref>{{cite journal | author = Pál C ''et al.'' | title = An integrated view of protein evolution | journal = Nat Rev Genet | volume = 7 |  pages = 337-48 | year = 2006 | id = PMID 16619049}}</ref> Genetic recombination can also be involved in DNA repair.<ref>{{cite journal | author = O'Driscoll M, Jeggo P | title = The role of double-strand break repair - insights from human genetics | journal = Nat Rev Genet | volume = 7 | pages = 45-54 | year = 2006 | id = PMID 16369571}}</ref>
 
The most common form of recombination is [[chromosomal crossover|homologous recombination]], where the two chromosomes involved share very similar sequences. However, recombination can also damage cells, by producing [[chromosomal translocation]]s and genetic abnormalities. Recombination reactions are catalyzed by ''recombinases'',<ref>{{cite journal | author = Sung P ''et al.'' | title = Rad51 recombinase and recombination mediators | journal = J Biol Chem | volume = 278 | pages = 42729-32 | year = 2003 | url = http://www.jbc.org/cgi/content/full/278/44/42729 | id = PMID 12912992}}</ref> which have a DNA-dependent ATPase activity. The recombinase makes a 'nick' in one strand of a DNA double helix, allowing the nicked strand to separate from its complementary strand and [[Annealing (biology)|anneal]] to one strand of the double helix on the opposite chromatid. A second nick allows the strand in the second chromatid to separate and anneal to the strand in the first helix, forming a ''cross-strand exchange'' (also called a [[Holliday junction]]). The Holliday junction is a tetrahedral junction structure which can be moved along the pair of chromosomes, swapping one strand for another. The recombination is then halted by cleavage of the junction and re-ligation of the released DNA.<ref>{{cite journal | author = Dickman M ''et al.'' | title = The RuvABC resolvasome | journal = Eur J Biochem | volume = 269 | pages = 5492-501 | year = 2002 | id = PMID 12423347}}</ref>


Another group of DNA-binding proteins bind single-stranded DNA. In humans, replication protein A is the best-characterised member of this family, and is essential for most processes where the double helix is separated (including DNA replication, recombination and DNA repair).<ref>{{cite journal | author = Iftode C ''et al.''| title = Replication protein A (RPA): the eukaryotic SSB | journal = Crit Rev Biochem Mol Biol | volume = 34 | pages = 141-80 | year = 1999 | id = PMID 10473346}}</ref> These proteins seem to stabilize single-stranded DNA and protect it from forming [[stem loop]]s or being degraded by [[nuclease]]s.
==== DNA Methylation ====
DNA methylation is the addition of a methyl group to the fifth carbon of cytosine in effect creating a fifth base. It is a naturally occurring event that can affect many cell functions by inhibiting gene expression, esopecially in the case of foreign DNA. A lack of methylation has been associated with many diseases. On the other hand, methylation of gene p16, a tumor suppressing gene, is suspected to be an epigenetic abnormality occurring early in lung carcinogenesis.<ref>http://cancerres.aacrjournals.org/cgi/content/abstract/62/2/351</ref>  


Other proteins bind to particular DNA sequences. The most intensively studied of these are the [[transcription factors]]. Each of these proteins binds to a particular set of DNA sequences and thereby activates or inhibits the transcription of genes with these sequences close to their [[promoter]]s. Transcription factors do this in two ways. Some can bind the RNA polymerase responsible for transcription, either directly or through other mediator proteins; this locates the polymerase at the promoter and allows it to begin transcription.<ref>{{cite journal | author = Myers L, Kornberg R | title = Mediator of transcriptional regulation | journal = Ann Rev Biochem | volume = 69 | issue = | pages = 729-49 | year = | id = PMID 10966474}}</ref> Other transcription factors can bind enzymes that modify the histones at the promoter, this will change the accessibility of the DNA template to the polymerase.<ref>{{cite journal | author = Spiegelman B, Heinrich R | title = Biological control through regulated transcriptional coactivators | journal = Cell | volume = 119 |  pages = 157-67 | year = 2004 | id = PMID 15479634}}</ref>
<ref>Blood, Vol. 93 No. 12 (June 15), 1999: pp. 4059-4070 online: http://bloodjournal.hematologylibrary.org/cgi/content/full/93/12/4059#Top</ref> The expression of genes is influenced by the [[chromatin]] structure of a chromosome which may hinder or enhance accessibility of the gene. Regions of [[heterochromatin]] (with little or no gene expression) correlate with the [[methylation]] of [[cytosine]].<ref> For example, cytosine methylation, to produce [[5-Methylcytosine|5-methylcytosine]], is important for [[X-inactivation|X-chromosome inactivation]]. {{cite journal | author = Klose R, Bird A | title = Genomic DNA methylation: the mark and its mediators | journal = Trends Biochem Sci | volume = 31 |  pages = 89–97 | year = 2006 | id = PMID 16403636}}</ref>  


These DNA targets can occur throughout an organism's genome, so changes in the activity of one type of transcription factor in a given cell can affect the expression of many genes in that cell.<ref>{{cite journal | author = Li Z ''et al.'' | title = A global transcriptional regulatory role for c-Myc in Burkitt's lymphoma cells | url=http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=12808131 | journal = Proc Natl Acad Sci USA | volume = 100 | pages = 8164-9 | year = 2003 | id = PMID 12808131}}</ref> Consequently, these proteins are often the targets of the [[signal transduction]] processes that mediate responses to environmental changes or cellular differentiation and development. The specificity of transcription factor interactions with DNA arises because the proteins make multiple contacts to the edges of the DNA bases, allowing them to "read" the DNA sequence. Most of these interactions occur in the major groove, where the bases are most accessible.<ref name=Pabo/>
These structural changes to the DNA are one type of [[epigenetic]] change that can alter chromatin structure, and they are inheritable. ''Epigenetics'' refers to features of organisms that are stable over successive rounds of cell division but which do not involve changes in the underlying DNA sequence<ref>{{cite journal| title=Perceptions of epigenetics| author=Bird A| journal=Nature| volume=447| pages=396-8| year=2007}} PMID 17522671</ref>. Epigenetic changes are important in [[morphogenesis|cellular differentiation]], allowing cells to maintain different characteristics despite containing the same genomic material. Some epigenetic features can be inherited from one generation to the next.<ref>{{cite journal| title=Paramutation: from maize to mice| author=Chandler VL| journal=Cell| volume=128| pages=641-5| year=2007}}</ref>


===DNA-modifying enzymes===
==== Nucleases and ligases ====
====Nucleases and ligases====
Nucleases cut DNA strands by catalyzing the [[hydrolysis]] of the [[phosphodiester bond]]s (nucleases that hydrolyse nucleotides from the ends of DNA strands are called [[exonuclease]]s, while [[endonuclease]]s cut within strands). The most frequently-used nucleases in [[molecular biology]] are the [[restriction enzyme|restriction endonucleases]], which cut DNA at specific sequences. For instance, the EcoRV enzyme recognizes the 6-base sequence 5′-GAT|ATC-3′ and makes a cut at the vertical line. In nature, these enzymes protect [[bacteria]] against [[phage]] infection by digesting the phage DNA when it enters the bacterial cell, acting as part of the [[restriction modification system]].<ref>{{cite journal | author = Bickle T, Krüger D | title = Biology of DNA restriction | url=http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=372918&blobtype=pdf | journal = Microbiol Rev | volume = 57 |  pages = 434–50 | year = 1993 | id = PMID 8336674}}</ref> In technology, these sequence-specific nucleases are used in [[clone (genetics)|molecular cloning]] and [[DNA fingerprinting]].
Nucleases cut DNA strands by catalyzing the [[hydrolysis]] of the [[phosphodiester bond]]s (nucleases that hydrolyse nucleotides from the ends of DNA strands are called [[exonuclease]]s, while [[endonuclease]]s cut within strands). The most frequently-used nucleases in [[molecular biology]] are the [[restriction enzyme|restriction endonucleases]], which cut DNA at specific sequences. For instance, the EcoRV enzyme recognizes the 6-base sequence 5′-GAT|ATC-3′ and makes a cut at the vertical line. In nature, these enzymes protect [[bacteria]] against [[phage]] infection by digesting the phage DNA when it enters the bacterial cell, acting as part of the [[restriction modification system]].<ref>{{cite journal | author = Bickle T, Krüger D | title = Biology of DNA restriction | url=http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=372918&blobtype=pdf | journal = Microbiol Rev | volume = 57 |  pages = 434–50 | year = 1993 | id = PMID 8336674}}</ref> In technology, these sequence-specific nucleases are used in [[clone (genetics)|molecular cloning]] and [[DNA fingerprinting]].


[[DNA ligase]]s can rejoin cut or broken DNA strands, using the energy from either [[adenosine triphosphate]] or [[nicotinamide adenine dinucleotide]]. Ligases are particularly important in [[lagging strand]] DNA replication, as they join together the short segments of DNA produced at the [[replication fork]] into a complete copy of the DNA template. They are also used in [[DNA repair]] and [[genetic recombination]].<ref name=Doherty>{{cite journal | author = Doherty A, Suh S | title = Structural and mechanistic conservation in DNA ligases. | url=http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=11058099 | journal = Nucleic Acids Res | volume = 28 | pages = 4051–8 | year = 2000 | id = PMID 11058099}}</ref>
[[DNA ligase]]s can rejoin cut or broken DNA strands, using the energy from either [[adenosine triphosphate]] or [[nicotinamide adenine dinucleotide]]. Ligases are particularly important in [[lagging strand]] DNA replication, as they join together the short segments of DNA produced at the [[replication fork]] into a complete copy of the DNA template. They are also used in [[DNA repair]] and [[genetic recombination]].<ref name=Doherty>{{cite journal | author = Doherty A, Suh S | title = Structural and mechanistic conservation in DNA ligases. | url=http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=11058099 | journal = Nucleic Acids Res | volume = 28 | pages = 4051–8 | year = 2000 | id = PMID 11058099}}</ref>


====Topoisomerases and helicases====
==== Mutations ====
[[Image:Topisomerasesv2.jpg|thumb|250px|Topoisomerase activities illustrated with  on covalently closed circular DNA. Topisomerases can form supercoils in DNA, and can interconvert covalently closed circular DNA and their catenated forms.]]
DNA can be damaged by many different agents. [[Mutagen]]s are agents which can produce genetic [[mutation]]s - these are alterations of one DNA base to another base. Examples of mutagens include [[oxidizing agent]]s, [[alkylating agent]]s and high-energy [[electromagnetic radiation]] such as [[ultraviolet light]] and [[x-rays]].
[[Topoisomerase]]s have both nuclease and ligase activity, and they can change the amount of [[DNA supercoil|supercoiling]] in DNA. Some work by cutting the DNA helix and allowing one section to rotate; the enzyme then seals the DNA break.<ref>{{cite journal | author = Champoux J | title = DNA topoisomerases: structure, function, and mechanism | journal = Ann Rev Biochem | volume = 70 | issue = | pages = 369–413 | year = | url=http://www.fhcrc.org/science/labs/stoddard/MCB_542/champoux_review_2001.pdf | id = PMID 11395412}}</ref> Others can cut one DNA helix and then pass a second strand of DNA through this break, before rejoining the helix.<ref>{{cite journal | author = Schoeffler A, Berger J | title = Recent advances in understanding structure-function relationships in the type II topoisomerase mechanism | journal = Biochem Soc Trans | volume = 33 | pages = 1465–70 | year = 2005 | id = PMID 16246147}}</ref> Topoisomerases are required for many processes involving DNA, such as DNA replication and transcription.<ref name=Wang/>


[[Helicase]]s are a type of '[[molecular motor]]'; they use the chemical energy in [[nucleoside triphosphate]]s (predominantly [[Adenosine triphosphate|ATP]]) to break hydrogen bonds between bases and unwind the DNA double helix into single strands.<ref>{{cite journal | author = Tuteja N, Tuteja R | title = Unraveling DNA helicases. Motif, structure, mechanism and function | url=http://www.blackwell-synergy.com/links/doi/10.1111%2Fj.1432-1033.2004.04094.x | journal = Eur J Biochem | volume = 271 | pages = 1849–63 | year = 2004 | id = PMID 15128295}}</ref> These enzymes are essential for most processes where enzymes need to access the DNA bases.
''Lesions'' of  DNA, in which residues are changed to a structure that is not a normal feature of DNA, are different from mutations. However, damaged DNA can give rise to mutations, and indeed, some DNA repair processes are ''error prone'' and thus themselves generate mutations. Many mutations have no effect on the function of the genes but some may cause a change in gene expression and function leading to a new phenotype.


====Polymerases====
Ultraviolet radiation damages DNA mostly by producing [[thymine dimer]]s.<ref>{{cite journal | author = Douki T ''et al.'' | title = Bipyrimidine photoproducts rather than oxidative lesions are the main type of DNA damage involved in the genotoxic effect of solar ultraviolet radiation | journal = Biochemistry | volume = 42 |  pages = 9221-6 | year = 2003 | id = PMID 12885257}}</ref> Oxidants such as [[free radical]]s or [[hydrogen peroxide]] can cause several forms of damage, including base modifications (particularly of guanosine) as well as double-strand breaks.<ref>{{cite journal | author = Cadet J ''et al.'' | title = Hydroxyl radicals and DNA base damage | journal = Mutat Res | volume = 424 | issue = 1-2 | pages = 9-21 | year = 1999 | id = PMID 10064846}}</ref> It has been estimated that, in each human cell, about 500 bases suffer oxidative damage every day.<ref>{{cite journal | author = Shigenaga M ''et al.'' | title = Urinary 8-hydroxy-2'-deoxyguanosine as a biological marker of ''in vivo'' oxidative DNA damage | url=http://www.pnas.org/cgi/reprint/86/24/9697 | journal = Proc Natl Acad Sci USA | volume = 86 | pages = 9697-701 | year = 1989 | id = PMID 2602371}}</ref><ref>{{cite journal | author = Cathcart R ''et al.'' | title = Thymine glycol and thymidine glycol in human and rat urine: a possible assay for oxidative DNA damage | url=http://www.pnas.org/cgi/reprint/81/18/5633.pdf | journal = Proc Natl Acad Sci USA | volume = 81 | pages = 5633-7 | year = 1984 | id = PMID 6592579}}</ref> Of these lesions, the most damaging are double-strand breaks, as they can produce [[point mutation]]s, insertions and deletions from the DNA sequence, as well as [[chromosomal translocation]]s.<ref>{{cite journal | author = Valerie K, Povirk L | title = Regulation and mechanisms of mammalian double-strand break repair | journal = Oncogene | volume = 22 |  pages = 5792-812 | year = 2003 | id = PMID 12947387}}</ref>
Polymerases  synthesise polynucleotides from [[nucleoside triphosphate]]s. They add nucleotides onto the 3′ [[hydroxyl|hydroxyl group]] of the previous nucleotide in the DNA strand, so all polymerases work in a 5′ to 3′ direction.<ref name=Joyce>{{cite journal | author = Joyce C, Steitz T | title = Polymerase structures and function: variations on a theme? | url=http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=177480&blobtype=pdf | journal = J Bacteriol | volume = 177 | pages = 6321–9 | year = 1995 | id = PMID 7592405}}</ref> In the [[active site]] of these enzymes, the nucleoside triphosphate substrate base-pairs to a single-stranded polynucleotide template: this allows polymerases to synthesise the complementary strand of this template accurately.


[[DNA polymerase]]s copy DNA sequences. Accuracy is very important for this, so many polymerases have a [[Proofreading#Proofreading in biology|proofreading]] activity: they can recognizes the occasional mistakes that can occur during synthesis. These enzymes detect the lack of base pairing between mismatched nucleotides, and if a mismatch is detected, a 3′ to 5′ [[exonuclease]] activity is activated and the incorrect base is removed.<ref>{{cite journal | author = Hubscher U ''et al.'' | title = Eukaryotic DNA polymerases | journal = Annu Rev Biochem | volume = 71 |pages = 133–63 | year = | id = PMID 12045093}}</ref> In most organisms, DNA polymerases function in a large complex called the [[replisome]].
Many mutagens [[intercalation (chemistry)|intercalate]] into the space between two adjacent base pairs. These are mostly polycyclic, [[aromatic]], and planar molecules, and include [[ethidium]], [[proflavin]], [[daunomycin]], [[doxorubicin]] and [[thalidomide]]. For an intercalator to fit between base pairs, the bases must separate, distorting the DNA strand by unwinding of the double helix. These structural modifications inhibit transcription and replication processes, causing both toxicity and mutations. As a result, DNA intercalators are often [[carcinogen]]s. Nevertheless, because they can inhibit DNA transcription and replication, they are also used in [[chemotherapy]] to inhibit DNA-replication in rapidly-growing [[cancer]] cells.<ref name=brana>{{cite journal | author = Braña M ''et al.'' | title = Intercalators as anticancer drugs | journal = Curr Pharm Des | volume = 7 | pages = 1745-80 | year = 2001 | id = PMID 11562309}}</ref>


RNA-dependent DNA polymerases copy the sequence of an RNA strand into DNA. One example is [[reverse transcriptase]], which is a viral enzyme involved in the infection of cells by [[retrovirus]]es; another example is [[telomerase]], which is required for the replication of [[telomere]]s.<ref>{{cite journal | author = Tarrago-Litvak L ''et al.'' | title = The reverse transcriptase of HIV-1: from enzymology to therapeutic intervention | url=http://www.fasebj.org/cgi/reprint/8/8/497 | journal = FASEB J | volume = 8 | pages = 497–503 | year = 1994 | id = PMID 7514143}}</ref><ref name=Greider/> Telomerase is an unusual polymerase because it contains its own RNA template as part of its structure.<ref>{{cite journal |author=Nugent C, Lundblad V |title=The telomerase reverse transcriptase: components and regulation | url=http://www.genesdev.org/cgi/content/full/12/8/1073 | journal=Genes Dev |volume=12 |issue=8 | pages=1073&ndash;85 |year=1998 |pmid=9553037}}</ref>
There are also internal sources for mutagens. [[Free radical]]s are produced as a result of [[oxidative phosphorylation|cellular respiration]] and are an unavoidable consequence of living. It is also known that genomes have specific sequences called transposons that have the ability to move around within the genome; they are sometimes referred to as "''jumping genes''". There are many varieties of transposons, some can break chromosomes or cause deletions, but a common theme is that they cause insertional mutants at their "landing site". <ref> I think we need a more general review of all transposons here not just retrotransposons </ref>


Transcription is carried out by a [[RNA polymerase]] that copies a DNA sequence into RNA. The enzyme binds to a promoter and separates the DNA strands. It then copies the gene sequence into a mRNA transcript until it reaches a region of DNA called the ''[[terminator (genetics)|terminator]]'', where it halts and detaches from the DNA. RNA polymerase II, which transcribes most of the genes in the human genome, operates as part of a large protein complex with multiple regulatory and accessory subunits.<ref>{{cite journal | author = Martinez E | title = Multi-protein complexes in eukaryotic gene transcription | journal = Plant Mol Biol | volume = 50 | pages = 925–47 | year = 2002 | id = PMID 12516863}}</ref>
==== DNA Repair ====
Environmental factors such as heat and ultraviolet radiation can produce hundreds and even thousands of mistakes in one day.  It is crucial that DNA replication accuracy is maintained. Repair is made possible by the complementary structure of DNA. A diverse set of more than 50 repair mechanisms are available to the cell to correct the mistakes. Replication error, after proofreading, is estimated to be one error in 10,000,000,000 replications. <ref>Hanawalt, P.C., and Setlow, R.B. (eds) Molecular Mechanisms for Repair of DNA. Plenum Press New York.</ref>


==Genetic recombination==
In general the repair process includes the recognition of the damage, uncoiling of the damaged area, snipping out and removing the damaged piece, recreation of the damaged piece using the undamaged complementary as a guide, insertion of the correct nucleotide segment and proofreading the corrections. <ref>6 de Boer J, Hoeijmakers JH. Nucleotide excision repair and human syndromes. Carcinogenesis 2000; 21: 453-60. online: http://websites.afar.org/site/PageServer?pagename=IA_b_dna_6_r_proc</ref>
A DNA helix does not usually interact with other segments of DNA, and in human cells the different chromosomes even occupy different regions of the nucleus (called "chromosome territories").<ref>{{cite journal | author = Cremer T, Cremer C | title = Chromosome territories, nuclear architecture and gene regulation in mammalian cells | journal = Nat Rev Genet | volume = 2 |  pages = 292-301 | year = 2001 | id = PMID 11283701}}</ref> This physical separation of chromosomes is important for the ability of DNA to function as a stable repository for information, as one of the few times chromosomes interact is when they [[genetic recombination|recombine]]. Recombination is when two DNA helices break, swap a section and then rejoin. In eukaryotes, this usually occurs during [[meiosis]], when two [[chromatid]]s are paired together in the center of the cell. This allows chromosomes to exchange genetic information and produces new combinations of genes.<ref>{{cite journal | author = Pál C ''et al.'' | title = An integrated view of protein evolution | journal = Nat Rev Genet | volume = 7 |  pages = 337-48 | year = 2006 | id = PMID 16619049}}</ref> Genetic recombination can also be involved in DNA repair.<ref>{{cite journal | author = O'Driscoll M, Jeggo P | title = The role of double-strand break repair - insights from human genetics | journal = Nat Rev Genet | volume = 7 | pages = 45-54 | year = 2006 | id = PMID 16369571}}</ref> The most common form of recombination is [[chromosomal crossover|homologous recombination]], where the two chromosomes involved share very similar sequences. However, recombination can also damage cells, by producing [[chromosomal translocation]]s and genetic abnormalities. Recombination reactions are catalyzed by ''recombinases'',<ref>{{cite journal | author = Sung P ''et al.'' | title = Rad51 recombinase and recombination mediators | journal = J Biol Chem | volume = 278 | pages = 42729-32 | year = 2003 | url = http://www.jbc.org/cgi/content/full/278/44/42729 | id = PMID 12912992}}</ref> which have a DNA-dependent ATPase activity. The recombinase makes a 'nick' in one strand of a DNA double helix, allowing the nicked strand to separate from its complementary strand and [[Annealing (biology)|anneal]] to one strand of the double helix on the opposite chromatid. A second nick allows the strand in the second chromatid to separate and anneal to the strand in the first helix, forming a ''cross-strand exchange'' (also called a [[Holliday junction]]). The Holliday junction is a tetrahedral junction structure which can be moved along the pair of chromosomes, swapping one strand for another. The recombination is then halted by cleavage of the junction and re-ligation of the released DNA.<ref>{{cite journal | author = Dickman M ''et al.'' | title = The RuvABC resolvasome | journal = Eur J Biochem | volume = 269 | pages = 5492-501 | year = 2002 | id = PMID 12423347}}</ref>


==DNA and molecular evolution==
==== An insight into evolution ====
As well as being susceptible to largely random mutations (that usually affect just a single base), some regions of DNA are specialised to undergo dramatic, rapid, non-random rearrangements, or to undergo more subtle changes at a high frequency so that the expression of a gene is dramatically altered. Such rearrangements include various versions of [[site-specific recombination]]. This depends on enzymes that recognise particular sites on DNA and create novel structures such as insertions, deletions and inversions. For instance, DNA regions in the small genome of the bacterial virus P1 can invert, enabling different versions of tail fibers to be expressed in different viruses. Similarly, site-specific recombinase enzymes are responsible for mating type variation in yeast, and for flagellum type (phase) changes in the bacterium ''Salmonella enterica'' Typhimurium.
As well as being susceptible to largely random mutations (that usually affect just a single base), some regions of DNA are specialised to undergo dramatic, rapid, non-random rearrangements, or to undergo more subtle changes at a high frequency so that the expression of a gene is dramatically altered. Such rearrangements include various versions of [[site-specific recombination]]. This depends on enzymes that recognise particular sites on DNA and create novel structures such as insertions, deletions and inversions. For instance, DNA regions in the small genome of the bacterial virus P1 can invert, enabling different versions of tail fibers to be expressed in different viruses. Similarly, site-specific recombinase enzymes are responsible for mating type variation in yeast, and for flagellum type (phase) changes in the bacterium ''Salmonella enterica'' Typhimurium.


Line 173: Line 237:
Triplet repeats behave similarly, but are particularly suited to evolution of proteins with differing characteristics. In the clock-like ''period'' gene of the fruit fly, triplet repeats 'fine tune' an insect's biological clock in response to changes in environmental temperatures. Triplet repeats are widely distributed in genomes, and their high frequency of mutation is responsible for several genetically determined disorders in humans.<ref>Christopher Wills discusses the evolutionary significance of these concepts in ''The Runaway Brain: The Evolution of Human Uniqueness'' ISBN 0-00-654672-2 (1995)</ref>
Triplet repeats behave similarly, but are particularly suited to evolution of proteins with differing characteristics. In the clock-like ''period'' gene of the fruit fly, triplet repeats 'fine tune' an insect's biological clock in response to changes in environmental temperatures. Triplet repeats are widely distributed in genomes, and their high frequency of mutation is responsible for several genetically determined disorders in humans.<ref>Christopher Wills discusses the evolutionary significance of these concepts in ''The Runaway Brain: The Evolution of Human Uniqueness'' ISBN 0-00-654672-2 (1995)</ref>


==Uses in technology==
==Impact on society==
===Forensics ===
==== Forensics ====
[[Forensic science|Forensic scientists]] can use DNA in blood, semen, skin, saliva or hair to match samples collected at a crime scene to samples taken from possible suspects. This process is called [[genetic fingerprinting]] or more formally, DNA profiling. In DNA profiling, the lengths of variable sections of repetitive DNA (such as [[short tandem repeats]] and [[minisatellite]]s) are compared between people. This is usually very reliable for identifying the source of a sample,<ref>{{cite journal | author = Collins A, Morton N | title = Likelihood ratios for DNA identification | url=http://www.pnas.org/cgi/reprint/91/13/6007.pdf | journal = Proc Natl Acad Sci USA | volume = 91 | pages = 6007-11 | year = 1994 | id = PMID 8016106}}</ref> but identification can be complicated if the samples that are collected include DNA from several people.<ref>{{cite journal | author = Weir B ''et al.'' | title = Interpreting DNA mixtures | journal = J Forensic Sci | volume = 42 |  pages = 213-22 | year = 1997 | id = PMID 9068179}}</ref> DNA profiling was developed in 1984 by British geneticist Sir [[Alec Jeffreys]],<ref>{{cite journal | author = Jeffreys A ''et al.'' | title = Individual-specific 'fingerprints' of human DNA. | journal = Nature | volume = 316 | pages = 76-9 | year = 1985| id = PMID 2989708}}</ref> and first used in forensic science to convict Colin Pitchfork (and to clear the prime suspect) in the 1988 [[Enderby murders]] case.<ref>[http://www.forensic.gov.uk/forensic_t/inside/news/list_casefiles.php?case=1 Colin Pitchfork - first murder conviction on DNA evidence also clears the prime suspect] Forensic Science Service Accessed 23 Dec 2006</ref> People convicted of certain types of crimes may be required to provide a sample of DNA for a database. This has helped investigators solve old cases where only a DNA sample was obtained from the scene. DNA profiling can also be used to identify victims of mass casualty incidents.<ref>{{cite web |url=http://massfatality.dna.gov/Introduction/ |title=DNA Identification in Mass Fatality Incidents |date=September 2006 |publisher=National Institute of Justice}}</ref>
[[Forensic science|Forensic scientists]] can use DNA in blood, semen, skin, saliva or hair to match samples collected at a crime scene to samples taken from possible suspects. This process is called [[genetic fingerprinting]] or more formally, DNA profiling. In DNA profiling, the lengths of variable sections of repetitive DNA (such as [[short tandem repeats]] and [[minisatellite]]s) are compared between people. This is usually very reliable for identifying the source of a sample,<ref>{{cite journal | author = Collins A, Morton N | title = Likelihood ratios for DNA identification | url=http://www.pnas.org/cgi/reprint/91/13/6007.pdf | journal = Proc Natl Acad Sci USA | volume = 91 | pages = 6007-11 | year = 1994 | id = PMID 8016106}}</ref> but identification can be complicated if the samples that are collected include DNA from several people.<ref>{{cite journal | author = Weir B ''et al.'' | title = Interpreting DNA mixtures | journal = J Forensic Sci | volume = 42 |  pages = 213-22 | year = 1997 | id = PMID 9068179}}</ref>  
 
DNA profiling was developed in 1984 by British geneticist Sir [[Alec Jeffreys]],<ref>{{cite journal | author = Jeffreys A ''et al.'' | title = Individual-specific 'fingerprints' of human DNA. | journal = Nature | volume = 316 | pages = 76-9 | year = 1985| id = PMID 2989708}}</ref> and first used in forensic science to convict Colin Pitchfork (and to clear the prime suspect) in the 1988 [[Enderby murders]] case.<ref>[http://www.forensic.gov.uk/forensic_t/inside/news/list_casefiles.php?case=1 Colin Pitchfork - first murder conviction on DNA evidence also clears the prime suspect] Forensic Science Service Accessed 23 Dec 2006</ref> People convicted of certain types of crimes may be required to provide a sample of DNA for a database. This has helped investigators solve old cases where only a DNA sample was obtained from the scene. DNA profiling can also be used to identify victims of mass casualty incidents.<ref>{{cite web |url=http://massfatality.dna.gov/Introduction/ |title=DNA Identification in Mass Fatality Incidents |date=September 2006 |publisher=National Institute of Justice}}</ref>
 
==== Bioinformatics ====
One branch of [[bioinformatics]] involves the analysis of DNA sequence data; DNA from hundreds of different organisms has now been partially sequenced, and this information is stored in massive databases. The development of techniques to store and search DNA sequences has led to many applications in [[computer science]].<ref>Baldi, Pierre. Brunak, Soren. ''Bioinformatics: The Machine Learning Approach'' MIT Press (2001) ISBN 978-0-262-02506-5</ref>  


===Bioinformatics===
String-searching or 'matching' algorithms, which identify a given sequence of letters inside a larger sequence of letters, are used to search for specific sequences of nucleotides. The related problem of [[sequence alignment]] aims to identify [[homology (biology)|homologous]] sequences; these are sequences that are very similar but not identical. When two different genes in an organism have very similar sequences, this is evidence that, at some stage in evolution, a single gene was duplicated, and the sequences subsequently diverged (under different selection pressures) by incorporating different mutations. Identifying such holologies can give valuable clues about the likely function of novel genes. Similarly, identifying homologies between genes in different organisms can be used to reconstruct the [[phylogenetics|evolutionary]] relationships between organisms.<ref>{{cite journal | author = Sjölander K | title = Phylogenomic inference of protein molecular function: advances and challenges | url=http://bioinformatics.oxfordjournals.org/cgi/reprint/20/2/170 | journal = Bioinformatics | volume = 20 |  pages = 170-9 | year = 2004 | id = PMID 14734307}}</ref> Data sets representing entire genomes' worth of DNA sequences, such as those produced by the [[Human Genome Project]], are difficult to use without [[annotations]], which label the locations of genes and regulatory elements on each chromosome. Regions of DNA sequence that have patterns that are characteristic of protein- or RNA-coding genes can be identified by [[gene finding]] algorithms, allowing researchers to predict the presence of particular [[gene product]]s in an organism.<ref name="Mount">{{cite book|author = Mount DM | title = Bioinformatics: Sequence and Genome Analysis | edition = 2 | publisher = Cold Spring Harbor Laboratory Press | location | Cold Spring Harbor, NY | date = 2004 | isbn = 0879697121}}</ref>
One branch of [[bioinformatics]] involves the analysis of DNA sequence data; DNA from hundreds of different organisms has now been partially sequenced, and this information is stored in massive databases. The development of techniques to store and search DNA sequences has led to many applications in [[computer science]].<ref>Baldi, Pierre. Brunak, Soren. ''Bioinformatics: The Machine Learning Approach'' MIT Press (2001) ISBN 978-0-262-02506-5</ref> String-searching or 'matching' algorithms, which identify a given sequence of letters inside a larger sequence of letters, are used to search for specific sequences of nucleotides. The related problem of [[sequence alignment]] aims to identify [[homology (biology)|homologous]] sequences; these are sequences that are very similar but not identical. When two different genes in an organism have very similar sequences, this is evidence that, at some stage in evolution, a single gene was duplicated, and the sequences subsequently diverged (under different selection pressures) by incorporating different mutations. Identifying such holologies can give valuable clues about the likely function of novel genes. Similarly, identifying homologies between genes in different organisms can be used to reconstruct the [[phylogenetics|evolutionary]] relationships between organisms.<ref>{{cite journal | author = Sjölander K | title = Phylogenomic inference of protein molecular function: advances and challenges | url=http://bioinformatics.oxfordjournals.org/cgi/reprint/20/2/170 | journal = Bioinformatics | volume = 20 |  pages = 170-9 | year = 2004 | id = PMID 14734307}}</ref> Data sets representing entire genomes' worth of DNA sequences, such as those produced by the [[Human Genome Project]], are difficult to use without [[annotations]], which label the locations of genes and regulatory elements on each chromosome. Regions of DNA sequence that have patterns that are characteristic of protein- or RNA-coding genes can be identified by [[gene finding]] algorithms, allowing researchers to predict the presence of particular [[gene product]]s in an organism.<ref name="Mount">{{cite book|author = Mount DM | title = Bioinformatics: Sequence and Genome Analysis | edition = 2 | publisher = Cold Spring Harbor Laboratory Press | location | Cold Spring Harbor, NY | date = 2004 | isbn = 0879697121}}</ref>


===Molecular cloning===
==== Molecular cloning ====
The small chromosomes of bacteria have proved extraordinarily useful for analysing genetic mechanisms and genome structure in many organisms, including humans. This utility arose because of several important discoveries made by microbiologists in the 1950-70's that provided new laboratory tools for directly manipulating genes. The principal laboratory tools and techniques discovered in this period were:  
The small chromosomes of bacteria have proved extraordinarily useful for analysing genetic mechanisms and genome structure in many organisms, including humans. This utility arose because of several important discoveries made by microbiologists in the 1950-70's that provided new laboratory tools for directly manipulating genes. The principal laboratory tools and techniques discovered in this period were:  
* Compact circular plasmid molecules such as [[ColE1]] that were relatively easy to extract and purify from bacterial cells, and when inserted back inside living bacterial cells could serve as genetically stable carriers (''vectors'') of novel DNA fragments. These vectors were propagated in bacterial cell lines termed "clones". Since each plasmid vector in these clones carried a single DNA molecular fragment, these could be considered to be 'molecular clones'.
* Compact circular plasmid molecules such as [[ColE1]] that were relatively easy to extract and purify from bacterial cells, and when inserted back inside living bacterial cells could serve as genetically stable carriers (''vectors'') of novel DNA fragments. These vectors were propagated in bacterial cell lines termed "clones". Since each plasmid vector in these clones carried a single DNA molecular fragment, these could be considered to be 'molecular clones'.
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After the mid-1970's, re-insertion of recombinant DNA plasmids into living bacterial cells, such as those of ''Escherichia coli'' opened up many new approaches in [[biotechnology]]. These made it possible to manufacture, for example, human hormones such as [[insulin]] in microbial cell-based protein factories. When combined with other genetic techniques, the field of "recombinant DNA technology" opened up the possibility of decoding the gene sequence of whole genomes. This latter area is now usually referred to as [[genomics]], and includes the [[Human Genome Project]].
After the mid-1970's, re-insertion of recombinant DNA plasmids into living bacterial cells, such as those of ''Escherichia coli'' opened up many new approaches in [[biotechnology]]. These made it possible to manufacture, for example, human hormones such as [[insulin]] in microbial cell-based protein factories. When combined with other genetic techniques, the field of "recombinant DNA technology" opened up the possibility of decoding the gene sequence of whole genomes. This latter area is now usually referred to as [[genomics]], and includes the [[Human Genome Project]].
==Bringing it together==
On January 28, 2008, an international research consortium announced the 1000 Genomes Project involving sequencing the genomes of at least a thousand people from around the world to create the most detailed and medically useful picture
to date of human genetic variation. Drawing on the expertise of multidisciplinary research teams, the 1000 Genomes Project will develop a new map of the human genome that will provide a view of biomedically relevant DNA variations at a resolution unmatched by current resources.
“The 1000 Genomes Project will examine the human genome at a level of detail that
no one has done before,” said Richard Durbin, Ph.D., of the Wellcome Trust Sanger
Institute, who is co-chair of the consortium. “Such a project would have been
unthinkable only two years ago. Today, thanks to amazing strides in sequencing
technology, bioinformatics and population genomics, it is now within our grasp. So
we are moving forward to build a tool that will greatly expand and further accelerate
efforts to find more of the genetic factors involved in human health and disease.”
As with other major human genome reference projects, data from the 1000 Genomes
Project will be available to the worldwide scientific community through
freely accessible public databases.
One example of the impact on understanding the biological basis for schizophrenia, was reported in Scientific American.<ref>Nikhil Swaminathan, [http://www.sciam.com/article.cfm?id=new-genetic-model-schi A New, Genetic Model for Schizophrenia] ''Scientific American'' 2008, March 28.</ref>
<blockquote>The researchers determined which affected genes were likely to cause damage—and where in the body that damage that might occur. The flawed genes in the schizophrenia patients were overwhelmingly linked to changes in pathways responsible for communication between and within nerve cells. In fact, one gene, ERBB4, is known to code for a receptor that interacts with neuregulin 1, a protein that's been associated with the illness for a decade. 'The silver lining is that these new findings show us … that we were already on the right track,' Sebat says."</blockquote>
Some researchers believe that future advances in genetics will result in patient specific treatments, however, they also express concerns about the cost of such drugs which will be needed only by a few.
Recent advances also include the capability to take a skin cell of a patient with a disease, transform it into a stem cell, and then program it to grow into the particular kind of cell which is affected by the disease which then can be studied.
== Looking to the Future ==
What may be of great significance and importance to biology and science in general is the realization made clear by the Genome Project that knowing merely the sequence of events is not enough to understand how life works. Also made clear is the realization that a tremendous amount of information is contained not only in the objects of study but also in the relationships that they maintain. As a result, a new discipline has emerged in the form of "Systems Biology"  <ref>Drack, Manfred.,  Apfalter, Wilfried., Pouvreau, David.  (2007) On the Making of a System Theory of Life: Paul A. Weiss and Ludwig von Bertalanffy's Conceptual Connection.  ''The Quarterly Review of Biology'' 82(4), The University of Chicago, Chicago.</ref> An integrative system is a perspective defined by biologist Ludwig von Bertalanffy as elements in standing relationship taken as a whole.<ref>Bertalanffy, Ludwig von,. (1968) General System Theory. George Braziller, N.Y., N.Y.. </ref> Systems Biology  complements the traditional "mechanistic" methodology of investigating isolated entities with a further perspective focusing on the organization of those entities.  <ref> Pouvreau, David.  Drack, Manfred. (2007)  On the History of Ludwig von Bertalanffy's "General Systemology", and on its relationship to cybernetics. International Journal of General Systems Vol. 36, No. 3, June 2007, 282-337. Taylor & Francis ISSN 0408-1079 (print)  ISSN 1563-5104 (online) </ref>


==References==
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DNA (Deoxyribonucleic acid) provides the genetic information necessary for the development and reproduction of all living organisms and is often described as a genetic blueprint.[1] Every living organism has its own DNA code that is organized in the ladder-like structure of the DNA molecule as a series of complementary paired molecules called bases. DNA is found within the nucleus of many cells, including those of animal and plant life.

DNA functions as a template: information is transferred from the sequence of base pairs within the DNA, by a molecule called messenger RNA (mRNA), to an enzyme called a ribosome (a biochemical assembly machine). The ribosome translates the code by assembling a protein molecule from amino acids (the building blocks of proteins) according to the base pair sequence brought to it by the mRNA. Proteins are very complex molecules used for signaling, regulation, metabolism and structural components. Cells containing DNA in any one organism have the same DNA, but each different cell type will synthesize its own characteristic combination of proteins, some common to most cells, while others are more specialized and help to define the functions of that particular cell type.

It is the complementary structure of DNA which enables it to function as a template for translating the genetic code and the assembly of the proteins. This complementary structure also enables the double stranded DNA to be separated and replicated as two exact duplicates during cell division (replication). [2]

Shown here are the four "letters" of DNA. The complementary base pairs are red & yellow and blue & green. The sugars in the backbone are shown in light blue. The twin strands of DNA are held together by hydrogen bonds between bases in a ladderlike structure. A codon is composed of a sequence of three of complementary base pairs. Each codon codes for one amino acid residue. It is a series of codons, along with a start codon and three stop codons that is transcribed and translated into a protein molecule.


Overview

In most organisms, DNA is formed as a very long and narrow double-helix formation of two DNA strands coiled around each other in a head-to-toe "antiparallel" orientation. The strands provide structural support for a complementary pair of bases located between the strands (a base pair is like a letter of a genetic word). A sequence of three base pairs forms a codon (a DNA word) on the DNA strand that encodes the information for one amino acid residue. A series of codons, and associated start/stop codons (a DNA sentence or gene), form the genetic code for the selection of particular amino acids and their specific arrangement necessary for the assembly of a particular protein molecule. The protein molecules, as many as 20,000 different types, are used in the cell, or are transported, often via small containers (vesicles), to other areas of the organism.

Each single strand of DNA is a long biopolymer composed of repeating units called nucleotides. A nucleotide is a base linked to a sugar and phosphate group which form a sugar/phosphate backbone. Attached to each sugar molecule (deoxyribose) is one of the four bases:

The corresponding deoxynucleosides are:

  • Deoxyadenosine[7]
  • Thymidine[8]
  • Deoxyguanosine[9]
  • Deoxycytidine[10]

Double-stranded DNA is formed by a weak hydrogen bond between the bases holding the nucleotides together. Each base is a structural complement of its opposing base, so both together form the base pair. The complementarity base pairs, A&T, C&G, are identical in size and shape and only one of the four arrangements - TA, AT, GC and CG, will fit between the backbones of double stranded DNA; e.g., adenine always pairs with thymine and guanine always pairs with cytosine. This complementarity, is at work in all DNA functions, and makes it possible for DNA to be copied and repaired relatively easily, while accurately preserving its information content. Thus it forms the basis of "semi-conservative DNA replication".[11]

Nuclear DNA is organized and stored as chromosomes within the nucleus. The nucleus is a double membrane separating the DNA from the cytoplasm of the cell enabling certain processing to occur prior to protein synthesis. Each chromosome holds hundreds or thousands of genes. A gene can be described in different ways but in general can be thought of as a whole unit of genetic information.

At conception for the human animal, the male sperm (a half-stranded DNA with a protein coat), and female ovum (an unfertilized egg also containing a single strand of DNA), each contribute 23 chromosomes for a total of 46 chromosomes in the fertilized embryo. The total sum of chromosomes is called the karyotype in eukaryotes (organisms such as plants, yeasts and animals whose cells have a nucleus)

Some organelles in eukaryotic cells (mitochondria and chloroplasts) have their own DNA with a similar organization to bacterial genomes. This DNA encodes for some of the functions in these organelles. Both the mitochondrial DNA (mtDNA) and the chloroplast DNA (cpDNA) originate in the female egg, so the organelle DNA is always inherited from the mother. Some cells, such as blood cells, do not have a nucleus and do not contain DNA. In prokaryote cells (organisms such as common bacteria), DNA is located in a region called the nucleoid. Viruses have a single type of nucleic acid, either DNA or RNA, directly encased in a protein coat called the capsid.

The entire DNA sequence of genes as a whole in any organism is called its genome. The genome provides the necessary genetic instructions to produce the phenotype, the outward physical manifestation of an organism, as well as the necessary processes involved in the replication of nuclear DNA.

Seeking the secret of life

Important genetic discoveries in DNA research spanned many decades. It was taken for granted by early researchers that only a protein molecule was complex enough to contain genetic information. A major discovery included the unexpected realization that the seemingly simple DNA molecule, and not the more complex protein molecule, is responsible for the internally coded, inheritable information defining the genotype. A further significant discovery was that the paired bases exist in equal proportions. These initial discoveries led to the important discovery of the duplex structure of DNA, usually referred to as the "double-helix", that enables the complementary replication of DNA in living organisms. The most important feature of the duplex model is the introduction of the concept of complementarity. Complementarity has come to explain the entire sequence of events in the expression of genetic functions.[12]

Isolating genetic material

DNA was first isolated in 1869 by Friedrich Miescher who discovered a microscopic substance in the pus of discarded surgical bandages. Because it resided in the nuclei of cells, he called it "nuclein".[13] In 1929, Phoebus Levene's identified the base, sugar and phosphate nucleotide unit .[14] Levene suggested that DNA consisted of a string of nucleotide units linked together through the phosphate groups. However Levene thought the chain was short and the bases repeated in a fixed order.

In 1928, Frederick Griffith demonstrated a "transforming factor" that can transmit the ability of Pneumococcus bacteria to cause pneumonia in mice. Although DNA had been identified in cells, it was not considered a strong candidate for the genetic material due to its simple form.

In 1943, Oswald Theodore Avery extended Griffith's work and discovered that traits of the virulent form of Pneumococcus could be transferred to the avirulent form of the same bacteria by mixing killed virulent bacteria with the live avirulent form. Avery identified DNA as the transforming factor.[15] This discovery is considered by some to be a major breakthrough enabling new research methods and a new focus on DNA itself and therefore represents the birth of molecular biology.[16]

DNA's role in heredity was confirmed in 1953, when Alfred Hershey and Martha Chase in the Hershey-Chase experiment, showed that DNA is the genetic material of the T2 phage.[17] This experiment provided the crucial evidence that it was DNA itself, (which was shown to enter the cell), and not a protein,(which remained outside the cell), that was the carrier of information.

Discovering the double helix and code

In 1950, Erwin Chargaff published a paper in which he described something he found extraordinary: the ratios of adenine to thymine were equal, as well as cytosine to guanine. He called this the complementary situation, but later it became known as the Chargaff Ratios. This discovery would play a crucial role in determining the structure of DNA. [18]

As early as 1937, William Astbury produced the first X-ray diffraction patterns that showed that DNA had a regular structure.[19] But it was not until 1953, based on the high-quality X-ray diffraction images[20] taken by Rosalind Franklin and the information provided by Erwin Chargaff that the bases were paired, that James D. Watson and Francis Crick constructed a cardboard model that led to [20] what is now accepted as the first accurate model of DNA structure. Their discovery on the morning of February 28, 1953, was reported in the journal Nature.[21]

Experimental evidence for Watson and Crick's model was published in five articles in the same issue of Nature.[22] Of these, Franklin and Raymond Gosling's paper[23] saw the publication of the X-ray diffraction image [24], which was key in Watson and Crick's interpretation, as well as another article, co-authored by Maurice Wilkins and his colleagues.[25] Franklin and Gosling's subsequent paper identified the distinctions between the A and B structures of the double helix in DNA.[26] In 1962, Watson, Crick, and Maurice Wilkins jointly received the Nobel Prize in Physiology or Medicine (Franklin didn't share the prize with them as she had died earlier).[27]

In an influential presentation in 1957, Crick laid out the "central dogma" of molecular biology, which foretold the relationship between DNA, RNA, and proteins and articulated the "adaptor hypothesis".[28] Final confirmation of the replication mechanism that was implied by the double-helical structure followed in 1958 through the Meselson-Stahl experiment.[29] Further work by Crick and coworkers showed that the genetic code was based on non-overlapping triplets of bases, called codons, allowing Har Gobind Khorana, Robert W. Holley and Marshall Warren Nirenberg to decipher the genetic code.[30]

Big science: the Human Genome Project

Initially biologists could only clone and sequence genes one by one, which required large amounts of labor and time in laboratories that were in scattered locations. As technology improved in the 1980's, some scientists such as Craig Venter and Leroy Hood believed their research could focus on sequencing whole genomes and they advocated a era of big science epitomised by the Human Genome Project (HGP). Their goal was to automate the mapping and sequencing to produce resources that would give science a valuable shortcut to addressing the biology of the genome.

Leroy Hood designed DNA sequencing machines to automate the process and thus massively reduce the cost of large scale sequencing. The chemistry of dideoxy sequencing devised by Frederick Sanger in 1977 was still the primary tool but new fluorescent labeling techniques, polymerase chain reaction (PCR) and genomic BAC/YAC libraries, were technological advances that made automation possible. Craig Venter advocated a random "shotgun" approach in the form of sequencing a massive number of randomly picked expressed sequence tags (EST's). Each tag represented a cDNA clone and the whole collection represented a catalog of expressed genes in a genome. This approach transitioned to sequencing random BAC's from the whole genome and was coined shotgun sequencing.

The HGP started out as an academic pursuit that used the traditional and slower target driven approach, a methodological tactic of establishing unique genetic markers, breaking the DNA into smaller bits which were then sequenced and, using the markers as a guide, reassembled. The public consortium was joined by a private effort at Celera Genomics that used the shotgun sequencing approach and a race to finish the project ensued. With the use of computers the vast number of fragments from Celera were assembled using the framework established by the HGP and in June of 2000, the completion of the draft sequence was announced by the leaders of the public and private projects. In January of 2008, the 1000 Genome Project, a mapping of 1000 genomes, was announced.

Assembled according to code

Three-dimensional model of the structure of part of a DNA double helix.

DNA is structured as a tightly-associated repeating pair of molecules (nucleotides) [21][31] entwined in the shape of a double helix. Looking much like a ladder, a typical DNA strand is about 5cm long and only a few atoms in width. The nucleotide repeats contain both the backbone of the molecule, which holds the chain together, and a base, which is a complement of the other DNA strand's base and backbone.

Building blocks

The backbone of the DNA strand has alternating phosphate and sugar residues[32]: the sugar is the pentose (five carbon) sugar 2-deoxyribose. One of the major differences between DNA and RNA is the sugar: 2-deoxyribose is replaced by ribose in RNA.

The sugar molecules are joined together by phosphate groups that form phosphodiester bonds between the third and fifth carbon atoms in the sugar rings. A strand of DNA has a 'direction'. In a double helix, the direction of the nucleotides in one strand is opposite to that in the other strand. Because these bonds are asymmetric, this arrangement of DNA strands is called antiparallel. The asymmetric ends of a strand of DNA bases are referred to as the 5' (five prime) and 3' (three prime) ends.

The double helix is a right-handed spiral. As the DNA strands wind around each other, gaps, called the major and a minor grooves, between the two phosphate backbones reveal the sides of the bases inside (see animation). Two grooves twist around the surface of the double helix: the major groove is 22 Å wide and the minor groove is 12 Å wide.[33] The edges of the bases are more accessible in the major groove, so proteins like transcription factors that can bind to specific sequences in double-stranded DNA usually make contacts to the sides of the bases exposed in the major groove. [34] For many DNA: protein complexes, up to one-half of the contacts involve the DNA phosphate groups, and thus many DNA binding proteins have more positive amino acids (lysine and arginine) than usual.

The double helix is held together by weak hydrogen bonds between the complementary bases attached to the two strands. If many nucleotides are linked together, as in DNA, the polymer is referred to as a polynucleotide.[35]

Base pairing

Each type of base on one strand of DNA forming a bond with a complementary base on the other strand, is called base pairing'. Purines form hydrogen bonds to pyrimidines; for example, A bonds only to T, and C bonds only to G. This arrangement of two nucleotides joined together across the double helix is called a base pair.

The four bases in DNA are adenine (A), cytosine (C), guanine (G) and thymine (T), and these bases are attached to the sugar/phosphate to form the complete nucleotide. Adenine and guanine are fused five- and six-membered heterocyclic compounds called purines, while cytosine and thymine are six-membered rings called pyrimidines.[35] A fifth pyrimidine base, uracil (U), replaces thymine in RNA. Uracil is normally only found in DNA as a breakdown product of cytosine, but bacterial viruses contain uracil in their DNA.[36] In contrast, following synthesis of certain RNA molecules, many uracils are converted to thymines. This occurs mostly on structural and enzymatic RNAs like tRNAs and ribosomal RNA.[37]

In a double helix, the two strands are also held together by hydrophobic effects and by a variation of pi stacking.[38] Hydrogen bonds are weak, and can be broken and rejoined quite easily, so the two strands of DNA in a double helix can be pulled apart like a zipper, either by mechanical force or by high temperatures.[39] Usually the strands are separated by a helicase, a biological unwinding motor. Because the base pairs form a complementarity, the information in the double-stranded sequence of a DNA helix is duplicated on each of the separate complementary opposing strands. The reversible and specific interaction between complementary base pairs is vital in DNA replication. and is critical for all the functions of DNA in living organisms.

The two types of base pairs form different numbers of hydrogen bonds; A&T forms two hydrogen bonds, and G&C forms three, so the G&C base-pair is stronger than the A&T pair. Thus, long DNA helices with a high G&C content have strongly interacting strands, while short helices with high A&T content have weakly interacting strands.[40] Parts of the DNA double helix that need to separate easily tend to have a high A&T content, making the strands easier to pull apart.[41] The strength of this interaction can be measured by finding the temperature required to break the hydrogen bonds (their 'melting temperature'). When all the base pairs in a DNA double helix melt, the strands separate, leaving two single-stranded molecules in solution. Because base-pairing causes changes in the UV-visible spectrum of the bases, DNA melting can be monitored by observing the hypochronicity (or loss thereof) as a function of temperature. These molecules have no single shape, but some conformations are more stable than others.

Flow of information

There are many interactions that happen between DNA and other molecules to coordinate its functions. When cells divide, the genetic information must be duplicated to produce two complementary copies of DNA in a process called DNA replication. When a cell uses the information in a gene, the DNA sequence is copied into a complementary single strand of RNA in a process called transcription. Of the transcribed sequences, some are used to directly make a matching protein sequence by a process called translation (meaning translation from a nucleic acid polymer to an amino acid polymer). The other transcribed RNA sequences may have regulatory, structural or catalytic roles.

Replication

Further information: Replication of a circular bacterial chromosome
DNA-replication illustrated by the bacterial replication fork. The helix is unwound and both strands asymetrically replicate simultaneously as they unwind. The leading strand replicates continuously from the 3' end (see arrows), with the newest end of the forming strand facing into the replication fork. The lagging strand replicates by a series of fragments (Okazaki fragments placed end-to-end, with the newest ends facing away from the fork; the Okazaki fragments are later joined together by DNA ligase. During replication, DNA polymerase III proofreads for mismatched bases

For an organism to grow, its cells must multiply, and this occurs by cell division: one cell splits to create two new 'daughter' cells. When a cell divides it must make an exact copy of its DNA so that the two daughter cells have the same genetic information as the parent cell. DNA replication requires a complex set of proteins, each dedicated to one of several different tasks needed to replicate this large molecule in an orderly and precise fashion. The double-stranded complementary structure of DNA provides a simple mechanism for this replication. The two strands of DNA are separated by a helicase (an unwinding motor), and then each strand's complementary DNA sequence is recreated by an enzyme called DNA polymerase. This makes the complementary strand by finding the correct base (through complementary base pairing), and bonding it to the original strand. DNA polymerases can only extend a DNA strand in a 5' to 3' direction, so other mechanisms are needed to copy the asymetrical antiparallel strand of the double helix.[42] In this way, the base on the old strand dictates which base appears on the new strand, and the cell ends up, after proofreading, with a perfect copy of its DNA.

Further capacity for DNA replication with substantial rearrangement is provided by mechanisms for DNA movement, inversion, and duplication, illustrated by various mobile DNAs such as transposons and proviruses (which has major implications for understanding mechanisms of molecular evolution).

Helicases

Helicases are a type of 'molecular active unwinding motor'[43]used to break hydrogen bonds between bases and unwind the DNA double helix into single strands.[44] Helicases are essential for most processes where enzymes need to access the DNA bases. They use the chemical energy in nucleoside triphosphates (predominantly ATP)

The single-stranded DNA exposed by the activity of the helicase enzyme is quickly bound by single-strand DNA binding proteins. In humans, replication protein A is the best-characterised member of this family, and is essential for most processes where the double helix is separated (including DNA replication, recombination and DNA repair).[45] These proteins seem to stabilize single-stranded DNA and protect it from forming stem loops or being degraded by nucleases.

Topoisomerases

Topoisomerase activities illustrated with on covalently closed circular DNA. Topisomerases can form supercoils in DNA, and can interconvert covalently closed circular DNA and their catenated forms.

DNA can be 'twisted' in a process called DNA supercoiling. In its "relaxed" state, a DNA strand usually circles the axis of the double helix once every 10.4 base pairs, but if the DNA is twisted, the strands become more tightly or more loosely wound. If the DNA is twisted in the direction of the helix (positive supercoiling), the bases are held more tightly together. If they are twisted in the opposite direction (negative supercoiling) the bases come apart more easily. Topoisomerases have both nuclease and ligase activity, and they can change the amount of supercoiling in DNA. Most DNA has slight negative supercoiling that is introduced by topoisomerases.

These enzymes are needed to relieve the twisting stresses introduced into DNA strands during processes such as transcription and DNA replication.[46]When a section of the double helix is being unwound, the remaining sections can be tangled. Type 1 toppoisomerases work by cutting the DNA helix and allowing one section to rotate; the enzyme then seals the DNA break. Type 11 cuts one DNA helix and then pass a second strand of DNA through this break, before rejoining the helix.[47][48]

Polymerases

The replicative polymerases are required for the faithful replication of the genetic material and they perform this role by attaching the appropriate nucleotide to the nascent strand to match the template strand. [49]Accuracy is very important for this, so many polymerases have a proofreading activity which can recognize the occasional mistakes that can occur during synthesis. These enzymes detect the lack of base pairing between mismatched nucleotides, and if a mismatch is detected, a 3′ to 5′ exonuclease activity is activated and the incorrect base is removed.[50] In most organisms, DNA polymerases function in a large complex called the replisome.

Polymerases synthesise polynucleotides from nucleoside triphosphates. They add nucleotides onto the 3′ hydroxyl group of the previous nucleotide in the DNA strand, so all polymerases work in a 5′ to 3′ direction. In the active site of these enzymes, the nucleoside triphosphate substrate base-pairs to a single-stranded polynucleotide template: this allows polymerases to synthesise the complementary strand of this template accurately.

RNA-dependent DNA polymerases copy the sequence of an RNA strand into DNA. One example is reverse transcriptase, which is a viral enzyme involved in the infection of cells by retroviruses; another example is telomerase, which is required for the replication of telomeres. Telomerase is an unusual polymerase because it contains its own RNA template as part of its structure.[51]

Transcription

Transcription is carried out by a RNA polymerase that copies a DNA sequence into RNA. The enzyme binds to a promoter and separates the DNA strands. It then copies the gene sequence into a mRNA transcript until it reaches a region of DNA called the terminator, where it halts and detaches from the DNA. This complementary copy is then decoded by a ribosome that reads the RNA sequence by base-pairing the mRNA to a specific aminoacyl-tRNA; an amino acid carried by a transfer RNA (tRNA). There is one start codon (AUG, which also encodes for methionine) and three 'stop' or 'nonsense' codons (UAA, UGA and UAG) that signify the end of the coding region.

The genetic code consists of three-letter 'words' called codons formed from a sequence of three nucleotides. As there are four bases in three-letter combinations, there are 64 possible codons, and these encode the twenty standard amino acids. For example, the sequences ACU, CAG and UUU in mRNA are translated to threonine, glutamine and phenylalanine, respectively. Many amino acids, have more than one possible codon (for example, ACU and ACA both code for threonine).

RNA polymerase II, which transcribes most of the genes in the human genome, operates as part of a large protein complex with multiple regulatory and accessory subunits.[52]

Translation

After a gene that encodes a protein is transcribed to a messenger RNA (mRNA), the code is delivered to an RNA/protein complex, an multienzyme, called a ribosome. The code is transferred to the ribosome by tRNA, which then translates the genetic code in a step by step process and assembles a string of amino acids one by one until the a stop codon is reached at which time the completed polypeptide is released into the cytoplasm. Several ribosomes may move along the mRNA simultaneously.

Sense and antisense

When the double strand is separated, two antiparallel strands exist. The DNA sequence that is translated into protein is a "sense" sequence. The sequence on the opposite strand is the "antisense" sequence. Sense and antisense sequences co-exist on the same strand of DNA; in both prokaryotes and eukaryotes, antisense sequences are transcribed[53], and antisense RNAs might be involved in regulating gene expression.[54]. (See Micro RNA, RNA interference, sRNA.)

Nature of genes

DNA contains the genetic information that is the basis for living functions including growth, reproduction and evolution. This information is held in segments of the DNA called genes that may span in size from dozens of DNA base-pairs to many thousands of base-pairs. All humans have essentially the same genes, but have slightly different DNA; on average, the DNA of two individuals differs at about three million bases. These differences are rarely in the protein-coding sequences of genes, but can affect how particular genes are regulated —, exactly where in the body a gene is expressed, how intensely it is expressed, or how expression is regulated by other genes or by environmental factors. These slight differences help to make every human being unique. By comparison, the genome of our closest living relative, the chimpanzee, differs from the human genome by about 30 million bases. [55]

DNA usually occurs as several large, linear chromosomes, each of which may contain hundreds or thousands of genes in eukaryotes. The complete set of chromosomes in a cell makes up its genome; the human genome has about three billion base pairs of DNA arranged into 46 chromosomes [56] and contains about 20,000 genes.[57] Prokaryotes generally have a single large circular chromosome, but they often possess other miniature chromosomes called plasmids.

The elusive definition

Gene comes from a Greek word meaning "to give birth to". Our understanding of the role genes play in cells, has been continually revised throughout the history of genetics. This has led to several definitions of a gene starting from abstract concepts of inheritable "factors" whose composition was unknown. One way to define a gene is simply as a segment of DNA that is transcribed into RNA - that is - the gene is a unit of transcription. This definition encompasses genes for non-coding RNAs, such as ribosomal RNA (rRNA) and transfer RNA (tRNA), as well as messenger RNA (mRNA) which is used for encoding the sequences of proteins. As defined in this case, a gene then is that whole unit of genetic information which is transcribed and translated into proteins.

A second approach is to define a gene as a region of DNA that encodes a single polypeptide. By this definition, any particular mRNA transcription unit can contain more than one gene, and thus a mRNA can carry regions encoding one or more polypeptides. Such a multi-genic transcription unit is called an operon and are common in prokaryotic cells.Both these definitions are similar to a "bead on a string" analogy with distinct genes as sequentially ordered units along a chromosome.

A more fuzzy definition considers genes as units of biological function. This definition can include cis-acting sequences of DNA that are not transcribed and flank a coding region. They act as specific binding sites for a variety of transcription factor proteins involved with regulating gene expression. Examples of such sequences are enhancers, promoters and operators. In this model the "bead on a string" analogy breaks down since the cis-acting factors from different genes do overlap and this is closer to the reality of gene structure in a chromosome.

Because of these various factors, the exact number of genes in a human organism has not yet been determined.[58]

Expression of genes

How genes are regulated — how they are turned on or off — is an important topic in modern biology, and research continually yields surprising insights into how phenotypic traits and biological adaptations are determined.

In the 1950's, investigations of the bacterium Escherichia coli led to the recognition that the region upstream of a transcribed region provides a place for the enzyme RNA polymerase to attach to DNA and start transcribing RNA in the 5' to 3' direction of the nucleic acid chain. The site at which this occurs came to be called the promoter. Other regulatory proteins (such as repressors) influence transcription by binding to a region near to or overlapping the promoter, called the operator. In the early years of modern genetics, emphasis was given to transcriptional regulation as an important and common means of modulating gene expression, but today we realize that there are a wide range of mechanisms by which the expression of mRNA and proteins can be modulated in cells.

Many DNA sequences in prokaryotes and eukaryotes (and more in plasmids and viruses) have overlapping genes which may both occur in the same direction, on the same strand (parallel) or in opposite directions, on opposite strands (antiparallel).[59][60] In these cases, some DNA sequences encode one protein when read from 5′ to 3′ along one strand, and a different protein when read in the opposite direction (but still from 5′ to 3′) along the other strand. In bacteria, this overlap may be involved in regulating gene transcription,[60] while in viruses, overlapping genes increase the information that can be encoded within the small viral genome.[61] Another way of reducing genome size is seen in some viruses that contain linear or circular single-stranded DNA.[62]

Trans acting proteins

All of the functions of DNA depend on its interactions with proteins. Some of these interactions are non-specific, others are specific in that the protein can only bind to a particular DNA sequence. Some enzymes can also bind to DNA and of these, the polymerases that copy the DNA base sequence in transcription and DNA replication are particularly important.

Other proteins bind to particular DNA sequences. The most intensively studied of these are the transcription factors. Each of these proteins binds to a particular set of DNA sequences and thereby activates or inhibits the transcription of genes with these sequences close to their promoters. Transcription factors do this in two ways. Some can bind the RNA polymerase responsible for transcription, either directly or through other mediator proteins; this locates the polymerase at the promoter and allows it to begin transcription.[63] Other transcription factors can bind enzymes that modify the histones at the promoter, this will change the accessibility of the DNA template to the polymerase.[64]

These DNA targets can occur throughout an organism's genome, so changes in the activity of one type of transcription factor in a given cell can affect the expression of many genes in that cell.[65] Consequently, these proteins are often the targets of the signal transduction processes that mediate responses to environmental changes or cellular differentiation and development. The specificity of transcription factor interactions with DNA arises because the proteins make multiple contacts to the edges of the DNA bases, allowing them to "read" the DNA sequence. Most of these interactions occur in the major groove, where the bases are most accessible.[34]

The chromosome: DNA's home

Nuclear DNA is organized and stored in compacted form into chromosomes inside the nucleus of the cell. At conception, the male sperm and female ovum contribute 23 chromosomes each, for a total of 46 chromosomes in the fertilized embryo. Mitochondria have their own DNA which originates in the female egg as a complete double strand.

DNA is an enormously long, unbranched linear polymer containing many millions of nucleotides the order of which provides the genetic information. For example an average cell has DNA with about 3X109 nucleosides. If each nucleotide were a letter on the page of a large book,they would occupy a million pages. If DNA were stretched out it would measure about 5 cm. but it must be contained in a nucleus measuring 5X10-4 cm in diameter. To achieve the necessary compactness as well as maintain accessibility, DNA is folded in many ways. The folding is assisted by proteins called histones, their sum is known as chromatin. The nucleosome is the first order of folding, appearing as beads on a string under magnification. In this case the DNA wraps around a histone core shaped like a cylinder. The cylinders are then packed together as groups. The groups are then looped. The folding is necessary for maximum compactness and for accessibility of transcription processes.[66]

Histones

Nucleosome 2.jpg
Nucleosome (opposites attracts).JPG
Interaction of DNA with histones (shown in white, top). These proteins' basic amino acids (below left, blue) bind to the acidic phosphate groups on DNA (below right, red).

DNA is held within the chromosomes as a complex of DNA and structural proteins called histones, forming a compact structure called chromatin. In adition to the histones are a variety of proteins called non-histone chromosomal proteins. In prokaryotes many types of proteins are involved.[67] The histones form a disk-shaped complex called a nucleosome which has two complete turns of double-stranded DNA wrapped around it.

These interactions are formed by positively charged amino acid residues in the histones making ionic bonds to the acidic sugar-phosphate backbone of the DNA, and thereby are largely independent of the base sequence.[68] Chemical modifications of these basic amino acid residues include methylation, phosphorylation and acetylation.[69] These changes alter the strength of the interaction between the DNA and the histones, making the DNA more or less accessible to transcription factors and changing the rate of transcription.[70] Other non-specific DNA-binding proteins found in chromatin include the high-mobility group proteins, which bind preferentially to bent or distorted DNA.[71] These proteins are important in bending arrays of nucleosomes and arranging them into more complex chromatin structures.[72]

Enabling transcription

Not only does the chromosome compact DNA, it allows for transcription while in the compacted state.

Genomes

The human genome has about three billion base pairs of DNA arranged into 46 chromosomes[56] and contains 25-30,000 genes [57]; the simple nematode C. elegans has almost as many genes (more than 19,000)[73]. In eukaryotes, DNA is located mainly in the cell nucleus (there are also small amounts in mitochondria and chloroplasts). In prokaryotes, the DNA is in an irregularly shaped body in the cytoplasm called the nucleoid.[74] The DNA is usually in linear chromosomes in eukaryotes, and circular chromosomes in prokaryotes.

In many species, only a small fraction of the genome encodes protein: only about 1.5% of the human genome consists of protein-coding exons, while over 50% consists of non-coding repetitive sequences.[75] While most of the non-coding elements in human DNA were once considered "junk DNA" with no known function, recent studies suggest a variety of roles for these regions, such as RNA silencing[76] or gene swapping by transposable elements.[77]

Some other vertebrates, including the puffer fish Fugu have more compact genomes, and (for multicellular organisms) there seems to be no consistent relationship between the size of the genome and the complexity of the organism.[78] Some non-coding DNA sequences are now known to have a structural role in chromosomes. In particular, telomeres and centromeres contain few genes, but are important for the function and stability of chromosomes.[79] An abundant form of non-coding DNA in humans are pseudogenes, which are copies of genes that have been disabled by mutation;[80] these are usually just molecular 'fossils', but they can provide the raw genetic material for new genes.[81]

A recent challenge to the long-standing view that the human genome consists of relatively few genes along with a vast amount of "junk DNA" comes from the ENCyclopedia Of DNA Elements (ENCODE) consortium.[82][83] Their survey of the human genome shows that most of the DNA is transcribed into molecules of RNA. This broad pattern of transcription was unexpected, but whether these transcribed (but not translated) elements have any biological function is not yet clear.[83]

The good, the neutral and the ugly

Genetic recombination

A DNA helix does not usually interact with other segments of DNA, and in human cells the different chromosomes even occupy different regions of the nucleus (called "chromosome territories").[84] This physical separation of chromosomes is important for the ability of DNA to function as a stable repository for information, as one of the few times chromosomes interact is when they recombine.

Recombination is when two DNA helices break, swap a section and then rejoin. In eukaryotes, this usually occurs during meiosis, when two chromatids are paired together in the center of the cell. This allows chromosomes to exchange genetic information and produces new combinations of genes.[85] Genetic recombination can also be involved in DNA repair.[86]

The most common form of recombination is homologous recombination, where the two chromosomes involved share very similar sequences. However, recombination can also damage cells, by producing chromosomal translocations and genetic abnormalities. Recombination reactions are catalyzed by recombinases,[87] which have a DNA-dependent ATPase activity. The recombinase makes a 'nick' in one strand of a DNA double helix, allowing the nicked strand to separate from its complementary strand and anneal to one strand of the double helix on the opposite chromatid. A second nick allows the strand in the second chromatid to separate and anneal to the strand in the first helix, forming a cross-strand exchange (also called a Holliday junction). The Holliday junction is a tetrahedral junction structure which can be moved along the pair of chromosomes, swapping one strand for another. The recombination is then halted by cleavage of the junction and re-ligation of the released DNA.[88]

DNA Methylation

DNA methylation is the addition of a methyl group to the fifth carbon of cytosine in effect creating a fifth base. It is a naturally occurring event that can affect many cell functions by inhibiting gene expression, esopecially in the case of foreign DNA. A lack of methylation has been associated with many diseases. On the other hand, methylation of gene p16, a tumor suppressing gene, is suspected to be an epigenetic abnormality occurring early in lung carcinogenesis.[89]

[90] The expression of genes is influenced by the chromatin structure of a chromosome which may hinder or enhance accessibility of the gene. Regions of heterochromatin (with little or no gene expression) correlate with the methylation of cytosine.[91]

These structural changes to the DNA are one type of epigenetic change that can alter chromatin structure, and they are inheritable. Epigenetics refers to features of organisms that are stable over successive rounds of cell division but which do not involve changes in the underlying DNA sequence[92]. Epigenetic changes are important in cellular differentiation, allowing cells to maintain different characteristics despite containing the same genomic material. Some epigenetic features can be inherited from one generation to the next.[93]

Nucleases and ligases

Nucleases cut DNA strands by catalyzing the hydrolysis of the phosphodiester bonds (nucleases that hydrolyse nucleotides from the ends of DNA strands are called exonucleases, while endonucleases cut within strands). The most frequently-used nucleases in molecular biology are the restriction endonucleases, which cut DNA at specific sequences. For instance, the EcoRV enzyme recognizes the 6-base sequence 5′-GAT|ATC-3′ and makes a cut at the vertical line. In nature, these enzymes protect bacteria against phage infection by digesting the phage DNA when it enters the bacterial cell, acting as part of the restriction modification system.[94] In technology, these sequence-specific nucleases are used in molecular cloning and DNA fingerprinting.

DNA ligases can rejoin cut or broken DNA strands, using the energy from either adenosine triphosphate or nicotinamide adenine dinucleotide. Ligases are particularly important in lagging strand DNA replication, as they join together the short segments of DNA produced at the replication fork into a complete copy of the DNA template. They are also used in DNA repair and genetic recombination.[95]

Mutations

DNA can be damaged by many different agents. Mutagens are agents which can produce genetic mutations - these are alterations of one DNA base to another base. Examples of mutagens include oxidizing agents, alkylating agents and high-energy electromagnetic radiation such as ultraviolet light and x-rays.

Lesions of DNA, in which residues are changed to a structure that is not a normal feature of DNA, are different from mutations. However, damaged DNA can give rise to mutations, and indeed, some DNA repair processes are error prone and thus themselves generate mutations. Many mutations have no effect on the function of the genes but some may cause a change in gene expression and function leading to a new phenotype.

Ultraviolet radiation damages DNA mostly by producing thymine dimers.[96] Oxidants such as free radicals or hydrogen peroxide can cause several forms of damage, including base modifications (particularly of guanosine) as well as double-strand breaks.[97] It has been estimated that, in each human cell, about 500 bases suffer oxidative damage every day.[98][99] Of these lesions, the most damaging are double-strand breaks, as they can produce point mutations, insertions and deletions from the DNA sequence, as well as chromosomal translocations.[100]

Many mutagens intercalate into the space between two adjacent base pairs. These are mostly polycyclic, aromatic, and planar molecules, and include ethidium, proflavin, daunomycin, doxorubicin and thalidomide. For an intercalator to fit between base pairs, the bases must separate, distorting the DNA strand by unwinding of the double helix. These structural modifications inhibit transcription and replication processes, causing both toxicity and mutations. As a result, DNA intercalators are often carcinogens. Nevertheless, because they can inhibit DNA transcription and replication, they are also used in chemotherapy to inhibit DNA-replication in rapidly-growing cancer cells.[101]

There are also internal sources for mutagens. Free radicals are produced as a result of cellular respiration and are an unavoidable consequence of living. It is also known that genomes have specific sequences called transposons that have the ability to move around within the genome; they are sometimes referred to as "jumping genes". There are many varieties of transposons, some can break chromosomes or cause deletions, but a common theme is that they cause insertional mutants at their "landing site". [102]

DNA Repair

Environmental factors such as heat and ultraviolet radiation can produce hundreds and even thousands of mistakes in one day. It is crucial that DNA replication accuracy is maintained. Repair is made possible by the complementary structure of DNA. A diverse set of more than 50 repair mechanisms are available to the cell to correct the mistakes. Replication error, after proofreading, is estimated to be one error in 10,000,000,000 replications. [103]

In general the repair process includes the recognition of the damage, uncoiling of the damaged area, snipping out and removing the damaged piece, recreation of the damaged piece using the undamaged complementary as a guide, insertion of the correct nucleotide segment and proofreading the corrections. [104]

An insight into evolution

As well as being susceptible to largely random mutations (that usually affect just a single base), some regions of DNA are specialised to undergo dramatic, rapid, non-random rearrangements, or to undergo more subtle changes at a high frequency so that the expression of a gene is dramatically altered. Such rearrangements include various versions of site-specific recombination. This depends on enzymes that recognise particular sites on DNA and create novel structures such as insertions, deletions and inversions. For instance, DNA regions in the small genome of the bacterial virus P1 can invert, enabling different versions of tail fibers to be expressed in different viruses. Similarly, site-specific recombinase enzymes are responsible for mating type variation in yeast, and for flagellum type (phase) changes in the bacterium Salmonella enterica Typhimurium.

More subtle mutations can occur in micro-satellite repeats (also called homopolymeric tracts of DNA). An example of such a structure are short DNA intervals where the same base is tandemly repeated, as in 5'-gcAAAAAAAAAAAttg-3', or a dinucleotide or even a triplet as in 5'- ATGATGATGATGATGATGATG-3'. DNA polymerase III is prone to make 'stuttering errors' at such repeats. As a consequence, changes in repeat number occur quite often during cell replication, and when they appear at a position where the spacing of nucleotide residues is critical for gene function, they can cause changes to the phenotype.

The stomach ulcer bacterium Helicobacter pylori is a good example of how homopolymeric tracts can enable quasi-directed evolution of particular genes. H. pylori has 46 genes that contain homopolymeric runs of nucleotides or dinucleotide repeats that are prone to frequent length changes as a consequence of stuttering errors during replication. These changes can lead to frequent reversible inactivation of these genes, or to changed gene transcription if the repeat is located in a regulatory sequence. This generates highly diverse populations of H. pylori in an individual human host, and this diversity helps the bacterium evade the immune system.[105]

Triplet repeats behave similarly, but are particularly suited to evolution of proteins with differing characteristics. In the clock-like period gene of the fruit fly, triplet repeats 'fine tune' an insect's biological clock in response to changes in environmental temperatures. Triplet repeats are widely distributed in genomes, and their high frequency of mutation is responsible for several genetically determined disorders in humans.[106]

Impact on society

Forensics

Forensic scientists can use DNA in blood, semen, skin, saliva or hair to match samples collected at a crime scene to samples taken from possible suspects. This process is called genetic fingerprinting or more formally, DNA profiling. In DNA profiling, the lengths of variable sections of repetitive DNA (such as short tandem repeats and minisatellites) are compared between people. This is usually very reliable for identifying the source of a sample,[107] but identification can be complicated if the samples that are collected include DNA from several people.[108]

DNA profiling was developed in 1984 by British geneticist Sir Alec Jeffreys,[109] and first used in forensic science to convict Colin Pitchfork (and to clear the prime suspect) in the 1988 Enderby murders case.[110] People convicted of certain types of crimes may be required to provide a sample of DNA for a database. This has helped investigators solve old cases where only a DNA sample was obtained from the scene. DNA profiling can also be used to identify victims of mass casualty incidents.[111]

Bioinformatics

One branch of bioinformatics involves the analysis of DNA sequence data; DNA from hundreds of different organisms has now been partially sequenced, and this information is stored in massive databases. The development of techniques to store and search DNA sequences has led to many applications in computer science.[112]

String-searching or 'matching' algorithms, which identify a given sequence of letters inside a larger sequence of letters, are used to search for specific sequences of nucleotides. The related problem of sequence alignment aims to identify homologous sequences; these are sequences that are very similar but not identical. When two different genes in an organism have very similar sequences, this is evidence that, at some stage in evolution, a single gene was duplicated, and the sequences subsequently diverged (under different selection pressures) by incorporating different mutations. Identifying such holologies can give valuable clues about the likely function of novel genes. Similarly, identifying homologies between genes in different organisms can be used to reconstruct the evolutionary relationships between organisms.[113] Data sets representing entire genomes' worth of DNA sequences, such as those produced by the Human Genome Project, are difficult to use without annotations, which label the locations of genes and regulatory elements on each chromosome. Regions of DNA sequence that have patterns that are characteristic of protein- or RNA-coding genes can be identified by gene finding algorithms, allowing researchers to predict the presence of particular gene products in an organism.[114]

Molecular cloning

The small chromosomes of bacteria have proved extraordinarily useful for analysing genetic mechanisms and genome structure in many organisms, including humans. This utility arose because of several important discoveries made by microbiologists in the 1950-70's that provided new laboratory tools for directly manipulating genes. The principal laboratory tools and techniques discovered in this period were:

  • Compact circular plasmid molecules such as ColE1 that were relatively easy to extract and purify from bacterial cells, and when inserted back inside living bacterial cells could serve as genetically stable carriers (vectors) of novel DNA fragments. These vectors were propagated in bacterial cell lines termed "clones". Since each plasmid vector in these clones carried a single DNA molecular fragment, these could be considered to be 'molecular clones'.
  • Convenient methods for extracting plasmid DNA from cells, physical analysis of this DNA, and reinsertion of circular plasmid DNA back inside living cells. The main method for DNA re-insertion is termed DNA transformation - that is, direct uptake of naked DNA molecules by cells. One technique that assisted DNA transformation was the use of selectable genetic markers, and plasmid-borne bacterial antibiotic resistance provided such markers in the form of traits like ampicillin resistance and tetracycline resistance.
  • Restriction endonucleases such as the enzymes EcoRI or HindIII, were found to be useful for specifically digesting DNA at particular sites and creating novel combinations of DNA fragments in the laboratory.
  • Restriction enzymes enabled re-annealing different DNA fragments, such as circular plasmid DNA which had been linearised at a single EcoRI restriction endonuclease target site together with another fragment, say an EcoRI generated fragment of a human chromosome. By sealing together two such fragments with the enzyme DNA ligase, novel hybrid-plasmid molecules could be created in which "foreign" DNA inserts were carried in a chimeric or hybrid plasmid, often called a recombinant DNA molecule.

After the mid-1970's, re-insertion of recombinant DNA plasmids into living bacterial cells, such as those of Escherichia coli opened up many new approaches in biotechnology. These made it possible to manufacture, for example, human hormones such as insulin in microbial cell-based protein factories. When combined with other genetic techniques, the field of "recombinant DNA technology" opened up the possibility of decoding the gene sequence of whole genomes. This latter area is now usually referred to as genomics, and includes the Human Genome Project.

Bringing it together

On January 28, 2008, an international research consortium announced the 1000 Genomes Project involving sequencing the genomes of at least a thousand people from around the world to create the most detailed and medically useful picture to date of human genetic variation. Drawing on the expertise of multidisciplinary research teams, the 1000 Genomes Project will develop a new map of the human genome that will provide a view of biomedically relevant DNA variations at a resolution unmatched by current resources.

“The 1000 Genomes Project will examine the human genome at a level of detail that no one has done before,” said Richard Durbin, Ph.D., of the Wellcome Trust Sanger Institute, who is co-chair of the consortium. “Such a project would have been unthinkable only two years ago. Today, thanks to amazing strides in sequencing technology, bioinformatics and population genomics, it is now within our grasp. So we are moving forward to build a tool that will greatly expand and further accelerate efforts to find more of the genetic factors involved in human health and disease.”

As with other major human genome reference projects, data from the 1000 Genomes Project will be available to the worldwide scientific community through freely accessible public databases.

One example of the impact on understanding the biological basis for schizophrenia, was reported in Scientific American.[115]

The researchers determined which affected genes were likely to cause damage—and where in the body that damage that might occur. The flawed genes in the schizophrenia patients were overwhelmingly linked to changes in pathways responsible for communication between and within nerve cells. In fact, one gene, ERBB4, is known to code for a receptor that interacts with neuregulin 1, a protein that's been associated with the illness for a decade. 'The silver lining is that these new findings show us … that we were already on the right track,' Sebat says."

Some researchers believe that future advances in genetics will result in patient specific treatments, however, they also express concerns about the cost of such drugs which will be needed only by a few. Recent advances also include the capability to take a skin cell of a patient with a disease, transform it into a stem cell, and then program it to grow into the particular kind of cell which is affected by the disease which then can be studied.

Looking to the Future

What may be of great significance and importance to biology and science in general is the realization made clear by the Genome Project that knowing merely the sequence of events is not enough to understand how life works. Also made clear is the realization that a tremendous amount of information is contained not only in the objects of study but also in the relationships that they maintain. As a result, a new discipline has emerged in the form of "Systems Biology" [116] An integrative system is a perspective defined by biologist Ludwig von Bertalanffy as elements in standing relationship taken as a whole.[117] Systems Biology complements the traditional "mechanistic" methodology of investigating isolated entities with a further perspective focusing on the organization of those entities. [118]

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