# DNA

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For a non-technical introduction to the topic, see Introduction to genetics.

Deoxyribonucleic acid (DNA) is a nucleic acid that contains the genetic instructions used in the development and functioning of all known living organisms and some viruses. The main role of DNA molecules is the long-term storage of information. DNA is often compared to a set of blueprints or a recipe, or a code, since it contains the instructions needed to construct other components of cells, such as proteins and RNA molecules. The DNA segments that carry this genetic information are called genes, but other DNA sequences have structural purposes, or are involved in regulating the use of this genetic information.

Chemically, DNA consists of two long polymers of simple units called nucleotides, with backbones made of sugars and phosphate groups joined by ester bonds. These two strands run in opposite directions to each other. Attached to each sugar is one of four types of molecules called bases. It is the sequence of these four bases along the backbone that encodes information. This information is read using the genetic code, which specifies the sequence of the amino acids within proteins. The code is read by copying stretches of DNA into the related nucleic acid RNA, in a process called transcription.

Within cells, DNA is organized into structures called chromosomes. These chromosomes are duplicated before cells divide, in a process called DNA replication. Eukaryotic organisms (animals, plants, fungi, and protists) store their DNA inside the cell nucleus, while in prokaryotes (bacteria and archae) it is found in the cell's cytoplasm. Within the chromosomes, chromatin proteins such as histones compact and organize DNA. These compact structures guide the interactions between DNA and other proteins, helping control which parts of the DNA are transcribed.

## PropertiesEdit

DNA is a long polymer made from repeating units called nucleotides.[1][2] The DNA chain is 22 to 26 Ångströms wide (2.2 to 2.6 nanometres), and one nucleotide unit is 3.3 Å (0.33 nm) long.[3] Although each individual repeating unit is very small, DNA polymers can be enormous molecules containing millions of nucleotides. For instance, the largest human chromosome, chromosome number 1, is approximately 220 million base pairs long.[4]

In living organisms, DNA does not usually exist as a single molecule, but instead as a tightly-associated pair of molecules.[5][6] These two long strands entwine like vines, in the shape of a double helix. The nucleotide repeats contain both the segment of the backbone of the molecule, which holds the chain together, and a base, which interacts with the other DNA strand in the helix. In general, a base linked to a sugar is called a nucleoside and a base linked to a sugar and one or more phosphate groups is called a nucleotide. If multiple nucleotides are linked together, as in DNA, this polymer is called a polynucleotide.[7]

The backbone of the DNA strand is made from alternating phosphate and sugar residues.[8] The sugar in DNA is 2-deoxyribose, which is a pentose (five-carbon) sugar. The sugars are joined together by phosphate groups that form phosphodiester bonds between the third and fifth carbon atoms of adjacent sugar rings. These asymmetric bonds mean a strand of DNA has a direction. In a double helix the direction of the nucleotides in one strand is opposite to their direction in the other strand. This arrangement of DNA strands is called antiparallel. The asymmetric ends of DNA strands are referred to as the 5′ (five prime) and 3′ (three prime) ends, with the 5' end being that with a terminal phosphate group and the 3' end that with a terminal hydroxyl group. One of the major differences between DNA and RNA is the sugar, with 2-deoxyribose being replaced by the alternative pentose sugar ribose in RNA.[6]

The DNA double helix is stabilized by hydrogen bonds between the bases attached to the two strands. The four bases found in DNA are adenine (abbreviated A), cytosine (C), guanine (G) and thymine (T). These four bases are attached to the sugar/phosphate to form the complete nucleotide, as shown for adenosine monophosphate.

These bases are classified into two types; adenine and guanine are fused five- and six-membered heterocyclic compounds called purines, while cytosine and thymine are six-membered rings called pyrimidines.[6] A fifth pyrimidine base, called uracil (U), usually takes the place of thymine in RNA and differs from thymine by lacking a methyl group on its ring. Uracil is not usually found in DNA, occurring only as a breakdown product of cytosine.

### GroovesEdit

The double helix is a right-handed spiral. As the DNA strands wind around each other, they leave gaps between each set of phosphate backbones, revealing the sides of the bases inside (see animation). There are two of these grooves twisting around the surface of the double helix: one groove, the major groove, is 22 Å wide and the other, the minor groove, is 12 Å wide.[10] The narrowness of the minor groove means that the edges of the bases are more accessible in the major groove. As a result, 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.[11]

### Base pairingEdit

Further information: Base pair

Each type of base on one strand forms a bond with just one type of base on the other strand. This is called complementary base pairing. Here, purines form hydrogen bonds to pyrimidines, with A bonding only to T, and C bonding only to G. This arrangement of two nucleotides binding together across the double helix is called a base pair. As hydrogen bonds are not covalent, they can be broken and rejoined relatively easily. The two strands of DNA in a double helix can therefore be pulled apart like a zipper, either by a mechanical force or high temperature.[12] As a result of this complementarity, all the information in the double-stranded sequence of a DNA helix is duplicated on each strand, which is vital in DNA replication. Indeed, this reversible and specific interaction between complementary base pairs is critical for all the functions of DNA in living organisms.[1]

Top, a GC base pair with three hydrogen bonds. Bottom, an AT base pair with two hydrogen bonds. Non-covalent hydrogen bonds between the pairs are shown as dashed lines.

The two types of base pairs form different numbers of hydrogen bonds, AT forming two hydrogen bonds, and GC forming three hydrogen bonds (see figures, left). DNA with high GC-content is more stable than DNA with low GC-content, but contrary to popular belief, this is not due to the extra hydrogen bond of a GC basepair but rather the contribution of stacking interactions (hydrogen bonding merely provides specificity of the pairing, not stability). [13] As a result, it is both the percentage of GC base pairs and the overall length of a DNA double helix that determine the strength of the association between the two strands of DNA. Long DNA helices with a high GC content have stronger-interacting strands, while short helices with high AT content have weaker-interacting strands.[14] In biology, parts of the DNA double helix that need to separate easily, such as the TATAAT Pribnow box in some promoters, tend to have a high AT content, making the strands easier to pull apart.[15] In the laboratory, the strength of this interaction can be measured by finding the temperature required to break the hydrogen bonds, their melting temperature (also called Tm value). When all the base pairs in a DNA double helix melt, the strands separate and exist in solution as two entirely independent molecules. These single-stranded DNA molecules have no single common shape, but some conformations are more stable than others.[16]

### Sense and antisenseEdit

Further information: Sense (molecular biology)

A DNA sequence is called "sense" if its sequence is the same as that of a messenger RNA copy that is translated into protein.[17] The sequence on the opposite strand is called the "antisense" sequence. Both sense and antisense sequences can exist on different parts of the same strand of DNA (i.e. both strands contain both sense and antisense sequences). In both prokaryotes and eukaryotes, antisense RNA sequences are produced, but the functions of these RNAs are not entirely clear.[18] One proposal is that antisense RNAs are involved in regulating gene expression through RNA-RNA base pairing.[19]

A few DNA sequences in prokaryotes and eukaryotes, and more in plasmids and viruses, blur the distinction between sense and antisense strands by having overlapping genes.[20] In these cases, some DNA sequences do double duty, encoding one protein when read along one strand, and a second protein when read in the opposite direction along the other strand. In bacteria, this overlap may be involved in the regulation of gene transcription,[21] while in viruses, overlapping genes increase the amount of information that can be encoded within the small viral genome.[22]

### SupercoilingEdit

Further information: DNA supercoil

DNA can be twisted like a rope in a process called DNA supercoiling. With DNA in its "relaxed" state, a 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.[23] If the DNA is twisted in the direction of the helix, this is positive supercoiling, and the bases are held more tightly together. If they are twisted in the opposite direction, this is negative supercoiling, and the bases come apart more easily. In nature, most DNA has slight negative supercoiling that is introduced by enzymes called topoisomerases.[24] These enzymes are also needed to relieve the twisting stresses introduced into DNA strands during processes such as transcription and DNA replication.[25]

### Alternative structuresEdit

Further information: Mechanical properties of DNA

DNA exists in many possible conformations.[8] However, only A-DNA, B-DNA, and Z-DNA have been observed in organisms. Which conformation DNA adopts depends on the sequence of the DNA, the amount and direction of supercoiling, chemical modifications of the bases and also solution conditions, such as the concentration of metal ions and polyamines.[26] Of these three conformations, the "B" form described above is most common under the conditions found in cells.[27] The two alternative double-helical forms of DNA differ in their geometry and dimensions.

The A form is a wider right-handed spiral, with a shallow, wide minor groove and a narrower, deeper major groove. The A form occurs under non-physiological conditions 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.[28][29] Segments of DNA where the bases have been chemically-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.[30] These unusual structures can be recognized by specific Z-DNA binding proteins and may be involved in the regulation of transcription.[31]

At the ends of the linear chromosomes are specialized regions of DNA called telomeres. The main function of these regions is to allow the cell to replicate chromosome ends using the enzyme telomerase, as the enzymes that normally replicate DNA cannot copy the extreme 3′ ends of chromosomes.[33] These specialized chromosome caps also help protect the DNA ends, and stop the DNA repair systems in the cell from treating them as damage to be corrected.[34] In human cells, telomeres are usually lengths of single-stranded DNA containing several thousand repeats of a simple TTAGGG sequence.[35]

These guanine-rich sequences may stabilize chromosome ends by forming structures of stacked sets of four-base units, rather than the usual base pairs found in other DNA molecules. Here, four guanine bases form a flat plate and these flat four-base units then stack on top of each other, to form a stable G-quadruplex structure.[36] These structures are stabilized by hydrogen bonding between the edges of the bases and chelation of a metal ion in the centre of each four-base unit.[37] Other structures can also be formed, with the central set of four bases coming from either a single strand folded around the bases, or several different parallel strands, each contributing one base to the central structure.

In addition to these stacked structures, telomeres also form large loop structures called telomere loops, or T-loops. Here, the single-stranded DNA curls around in a long circle stabilized by telomere-binding proteins.[38] At the very end of the T-loop, the single-stranded telomere DNA is held onto a region of double-stranded DNA by the telomere strand disrupting the double-helical DNA and base pairing to one of the two strands. This triple-stranded structure is called a displacement loop or D-loop.[36]

## Chemical modificationsEdit

Structure of cytosine with and without the 5-methyl group. After deamination the 5-methylcytosine has the same structure as thymine

### Base modificationsEdit

Further information: DNA methylation

The expression of genes is influenced by how the DNA is packaged in chromosomes, in a structure called chromatin. Base modifications can be involved in packaging, with regions of that have low or no gene expression usually containing high levels of methylation of cytosine bases. For example, cytosine methylation, produces 5-methylcytosine, which is important for X-chromosome inactivation.[39] The average level of methylation varies between organisms - the worm Caenorhabditis elegans lacks cytosine methylation, while vertebrates have higher levels, with up to 1% of their DNA containing 5-methylcytosine.[40] Despite the importance of 5-methylcytosine, it can deaminate to leave a thymine base, methylated cytosines are therefore particularly prone to mutations.[41] Other base modifications include adenine methylation in bacteria and the glycosylation of uracil to produce the "J-base" in kinetoplastids.[42][43]

### DamageEdit

Further information: Mutation

DNA can be damaged by many different sorts of mutagens, which change the DNA sequence. Mutagens include oxidizing agents, alkylating agents and also high-energy electromagnetic radiation such as ultraviolet light and X-rays. The type of DNA damage produced depends on the type of mutagen. For example, UV light can damage DNA by producing thymine dimers, which are cross-links between pyrimidine bases.[45] On the other hand, oxidants such as free radicals or hydrogen peroxide produce multiple forms of damage, including base modifications, particularly of guanosine, and double-strand breaks.[46] In each human cell, about 500 bases suffer oxidative damage per day.[47][48] Of these oxidative lesions, the most dangerous are double-strand breaks, as these are difficult to repair and can produce point mutations, insertions and deletions from the DNA sequence, as well as chromosomal translocations.[49]

Many mutagens fit into the space between two adjacent base pairs, this is called intercalating. Most intercalators are aromatic and planar molecules, and include Ethidium bromide, daunomycin, and doxorubicin. In order for an intercalator to fit between base pairs, the bases must separate, distorting the DNA strands by unwinding of the double helix. This inhibits both transcription and DNA replication, causing toxicity and mutations. As a result, DNA intercalators are often carcinogens, and benzopyrene diol epoxide, acridines, aflatoxin and ethidium bromide are well-known examples.[50][51][52] Nevertheless, due to their ability to inhibit DNA transcription and replication, these toxins are also used in chemotherapy to inhibit rapidly-growing cancer cells.[53]

## Biological functionsEdit

DNA usually occurs as linear chromosomes in eukaryotes, and circular chromosomes in prokaryotes. The set of chromosomes in a cell makes up its genome; the human genome has approximately 3 billion base pairs of DNA arranged into 46 chromosomes.[54] The information carried by DNA is held in the sequence of pieces of DNA called genes. Transmission of genetic information in genes is achieved via complementary base pairing. For example, in transcription, when a cell uses the information in a gene, the DNA sequence is copied into a complementary RNA sequence through the attraction between the DNA and the correct RNA nucleotides. Usually, this RNA copy is then used to make a matching protein sequence in a process called translation which depends on the same interaction between RNA nucleotides. Alternatively, a cell may simply copy its genetic information in a process called DNA replication. The details of these functions are covered in other articles; here we focus on the interactions between DNA and other molecules that mediate the function of the genome.

### Genes and genomesEdit

Further information: Cell nucleus, Chromatin, Chromosome, Gene, Noncoding DNA

Genomic DNA is located in the cell nucleus of eukaryotes, as well as small amounts in mitochondria and chloroplasts. In prokaryotes, the DNA is held within an irregularly shaped body in the cytoplasm called the nucleoid.[55] The genetic information in a genome is held within genes, and the complete set of this information in an organism is called its genotype. A gene is a unit of heredity and is a region of DNA that influences a particular characteristic in an organism. Genes contain an open reading frame that can be transcribed, as well as regulatory sequences such as promoters and enhancers, which control the transcription of the open reading frame.

In many species, only a small fraction of the total sequence of the genome encodes protein. For example, only about 1.5% of the human genome consists of protein-coding exons, with over 50% of human DNA consisting of non-coding repetitive sequences.[56] The reasons for the presence of so much non-coding DNA in eukaryotic genomes and the extraordinary differences in genome size, or C-value, among species represent a long-standing puzzle known as the "C-value enigma."[57] However, DNA sequences that do not code protein may still encode functional non-coding RNA molecules, which are involved in the regulation of gene expression.[58]

Some non-coding DNA sequences play structural roles in chromosomes. Telomeres and centromeres typically contain few genes, but are important for the function and stability of chromosomes.[34][60] An abundant form of non-coding DNA in humans are pseudogenes, which are copies of genes that have been disabled by mutation.[61] These sequences are usually just molecular fossils, although they can occasionally serve as raw genetic material for the creation of new genes through the process of gene duplication and divergence.[62]

### Transcription and translationEdit

Further information: Genetic code, Transcription (genetics), Protein biosynthesis

A gene is a sequence of DNA that contains genetic information and can influence the phenotype of an organism. Within a gene, the sequence of bases along a DNA strand defines a messenger RNA sequence, which then defines one or more protein sequences. The relationship between the nucleotide sequences of genes and the amino-acid sequences of proteins is determined by the rules of translation, known collectively as the genetic code. The genetic code consists of three-letter 'words' called codons formed from a sequence of three nucleotides (e.g. ACT, CAG, TTT).

In transcription, the codons of a gene are copied into messenger RNA by RNA polymerase. This RNA copy is then decoded by a ribosome that reads the RNA sequence by base-pairing the messenger RNA to transfer RNA, which carries amino acids. Since there are 4 bases in 3-letter combinations, there are 64 possible codons ($4^3$ combinations). These encode the twenty standard amino acids, giving most amino acids more than one possible codon. There are also three 'stop' or 'nonsense' codons signifying the end of the coding region; these are the TAA, TGA and TAG codons.

### ReplicationEdit

Further information: DNA replication

Cell division is essential for an organism to grow, but when a cell divides it must replicate the DNA in its genome so that the two daughter cells have the same genetic information as their parent. The double-stranded structure of DNA provides a simple mechanism for DNA replication. Here, the two strands are separated and then each strand's complementary DNA sequence is recreated by an enzyme called DNA polymerase. This enzyme makes the complementary strand by finding the correct base through complementary base pairing, and bonding it onto the original strand. As DNA polymerases can only extend a DNA strand in a 5′ to 3′ direction, different mechanisms are used to copy the antiparallel strands of the double helix.[63] In this way, the base on the old strand dictates which base appears on the new strand, and the cell ends up with a perfect copy of its DNA.

## Interactions with proteinsEdit

All the functions of DNA depend on interactions with proteins. These protein interactions can be non-specific, or the protein can bind specifically to a single DNA sequence. 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 proteinsEdit

 260px 260px
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).

Structural proteins that bind DNA are well-understood examples of non-specific DNA-protein interactions. Within chromosomes, DNA is held in complexes with structural proteins. These proteins organize the DNA into a compact structure called chromatin. In eukaryotes this structure involves DNA binding to a complex of small basic proteins called histones, while in prokaryotes multiple types of proteins are involved.[64][65] The histones form a disk-shaped complex called a nucleosome, which contains two complete turns of double-stranded DNA wrapped around its surface. These non-specific interactions are formed through basic residues in the histones making ionic bonds to the acidic sugar-phosphate backbone of the DNA, and are therefore largely independent of the base sequence.[66] Chemical modifications of these basic amino acid residues include methylation, phosphorylation and acetylation.[67] These chemical 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.[68] Other non-specific DNA-binding proteins in chromatin include the high-mobility group proteins, which bind to bent or distorted DNA.[69] These proteins are important in bending arrays of nucleosomes and arranging them into the larger structures that make up chromosomes.[70]

A distinct group of DNA-binding proteins are the DNA-binding proteins that specifically bind single-stranded DNA. In humans, replication protein A is the best-understood member of this family and is used in processes where the double helix is separated, including DNA replication, recombination and DNA repair.[71] These binding proteins seem to stabilize single-stranded DNA and protect it from forming stem-loops or being degraded by nucleases.

In contrast, other proteins have evolved to bind particular DNA sequences. The most intensively-studied of these are the various transcription factors, which are proteins that regulate transcription. Each transcription factor binds to one particular set of DNA sequences and activates or inhibits the transcription of genes that have these sequences close to their promoters. The transcription factors do this in two ways. Firstly, they 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.[73] Alternatively, transcription factors can bind enzymes that modify the histones at the promoter; this will change the accessibility of the DNA template to the polymerase.[74]

As these DNA targets can occur throughout an organism's genome, changes in the activity of one type of transcription factor can affect thousands of genes.[75] Consequently, these proteins are often the targets of the signal transduction processes that control responses to environmental changes or cellular differentiation and development. The specificity of these transcription factors' interactions with DNA come from the proteins making multiple contacts to the edges of the DNA bases, allowing them to "read" the DNA sequence. Most of these base-interactions are made in the major groove, where the bases are most accessible.[76]

### DNA-modifying enzymesEdit

#### Nucleases and ligasesEdit

Nucleases are enzymes that 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 shown to the left 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.[78] In technology, these sequence-specific nucleases are used in molecular cloning and DNA fingerprinting.

Enzymes called DNA ligases can rejoin cut or broken DNA strands.[79] 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.[79]

#### Topoisomerases and helicasesEdit

Topoisomerases are enzymes with both nuclease and ligase activity. These proteins change the amount of supercoiling in DNA. Some of these enzyme work by cutting the DNA helix and allowing one section to rotate, thereby reducing its level of supercoiling; the enzyme then seals the DNA break.[24] Other types of these enzymes are capable of cutting one DNA helix and then passing a second strand of DNA through this break, before rejoining the helix.[80] Topoisomerases are required for many processes involving DNA, such as DNA replication and transcription.[25]

Helicases are proteins that are a type of molecular motor. They use the chemical energy in nucleoside triphosphates, predominantly ATP, to break hydrogen bonds between bases and unwind the DNA double helix into single strands.[81] These enzymes are essential for most processes where enzymes need to access the DNA bases.

#### PolymerasesEdit

Polymerases are enzymes that synthesize polynucleotide chains from nucleoside triphosphates. The sequence of their products are copies of existing polynucleotide chains - which are called templates. These enzymes function by adding nucleotides onto the 3′ hydroxyl group of the previous nucleotide in a DNA strand. Consequently, all polymerases work in a 5′ to 3′ direction.[82] In the active site of these enzymes, the incoming nucleoside triphosphate base-pairs to the template: this allows polymerases to accurately synthesize the complementary strand of their template. Polymerases are classified according to the type of template that they use.

In DNA replication, a DNA-dependent DNA polymerase makes a DNA copy of a DNA sequence. Accuracy is vital in this process, so many of these polymerases have a proofreading activity. Here, the polymerase recognizes the occasional mistakes in the synthesis reaction by the lack of base pairing between the mismatched nucleotides. If a mismatch is detected, a 3′ to 5′ exonuclease activity is activated and the incorrect base removed.[83] In most organisms DNA polymerases function in a large complex called the replisome that contains multiple accessory subunits, such as the DNA clamp or helicases.[84]

RNA-dependent DNA polymerases are a specialized class of polymerases that copy the sequence of an RNA strand into DNA. They include reverse transcriptase, which is a viral enzyme involved in the infection of cells by retroviruses, and telomerase, which is required for the replication of telomeres.[85][33] Telomerase is an unusual polymerase because it contains its own RNA template as part of its structure.[34]

Transcription is carried out by a DNA-dependent RNA polymerase that copies the sequence of a DNA strand into RNA. To begin transcribing a gene, the RNA polymerase binds to a sequence of DNA called a promoter and separates the DNA strands. It then copies the gene sequence into a messenger RNA transcript until it reaches a region of DNA called the terminator, where it halts and detaches from the DNA. As with human DNA-dependent DNA polymerases, RNA polymerase II, the enzyme that transcribes most of the genes in the human genome, operates as part of a large protein complex with multiple regulatory and accessory subunits.[86]

## Genetic recombinationEdit

 250px 250px
Structure of the Holliday junction intermediate in genetic recombination. The four separate DNA strands are coloured red, blue, green and yellow.[87]
Further information: Genetic recombination

A DNA helix usually does not interact with other segments of DNA, and in human cells the different chromosomes even occupy separate areas in the nucleus called "chromosome territories".[88] This physical separation of different 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 during chromosomal crossover when they recombine. Chromosomal crossover is when two DNA helices break, swap a section and then rejoin.

Recombination allows chromosomes to exchange genetic information and produces new combinations of genes, which increases the efficiency of natural selection and can be important in the rapid evolution of new proteins.[89] Genetic recombination can also be involved in DNA repair, particularly in the cell's response to double-strand breaks.[90]

The most common form of chromosomal crossover is homologous recombination, where the two chromosomes involved share very similar sequences. Non-homologous recombination can be damaging to cells, as it can produce chromosomal translocations and genetic abnormalities. The recombination reaction is catalyzed by enzymes known as recombinases, such as RAD51.[91] The first step in recombination is a double-stranded break either caused by an endonuclease or damage to the DNA.[92] A series of steps catalyzed in part by the recombinase then leads to joining of the two helices by at least one Holliday junction, in which a segment of a single strand in each helix is annealed to the complementary strand in the other helix. The Holliday junction is a tetrahedral junction structure that can be moved along the pair of chromosomes, swapping one strand for another. The recombination reaction is then halted by cleavage of the junction and re-ligation of the released DNA.[93]

## EvolutionEdit

Further information: RNA world hypothesis

DNA contains the genetic information that allows all modern living things to function, grow and reproduce. However, it is unclear how long in the 4-billion-year history of life DNA has performed this function, as it has been proposed that the earliest forms of life may have used RNA as their genetic material.[82][94] RNA may have acted as the central part of early cell metabolism as it can both transmit genetic information and carry out catalysis as part of ribozymes.[95] This ancient RNA world where nucleic acid would have been used for both catalysis and genetics may have influenced the evolution of the current genetic code based on four nucleotide bases. This would occur since the number of unique bases in such an organism is a trade-off between a small number of bases increasing replication accuracy and a large number of bases increasing the catalytic efficiency of ribozymes.[96]

Unfortunately, there is no direct evidence of ancient genetic systems, as recovery of DNA from most fossils is impossible. This is because DNA will survive in the environment for less than one million years and slowly degrades into short fragments in solution.[97] Claims for older DNA have been made, most notably a report of the isolation of a viable bacterium from a salt crystal 250-million years old,[98] but these claims are controversial.[99][100]

## Uses in technologyEdit

### Genetic engineeringEdit

Further information: Molecular biology, nucleic acid methods and genetic engineering

Methods have been developed to purify DNA from organisms, such as phenol-chloroform extraction and manipulate it in the laboratory, such as restriction digests and the polymerase chain reaction. Modern biology and biochemistry make intensive use of these techniques in recombinant DNA technology. Recombinant DNA is a man-made DNA sequence that has been assembled from other DNA sequences. They can be transformed into organisms in the form of plasmids or in the appropriate format, by using a viral vector.[101] The genetically modified organisms produced can be used to produce products such as recombinant proteins, used in medical research,[102] or be grown in agriculture.[103][104]

### ForensicsEdit

Further information: Genetic fingerprinting

Forensic scientists can use DNA in blood, semen, skin, saliva or hair found at a crime scene to identify a matching DNA of an individual, such as a perpetrator. This process is called genetic fingerprinting, or more accurately, 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 method is usually an extremely reliable technique for identifying a matching DNA.[105] However, identification can be complicated if the scene is contaminated with DNA from several people.[106] DNA profiling was developed in 1984 by British geneticist Sir Alec Jeffreys,[107] and first used in forensic science to convict Colin Pitchfork in the 1988 Enderby murders case.[108]

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.[109] On the other hand, many convicted people have been released from prison on the basis of DNA techniques, which were not available when a crime had originally been committed.

### BioinformaticsEdit

Further information: Bioinformatics

Bioinformatics involves the manipulation, searching, and data mining of DNA sequence data. The development of techniques to store and search DNA sequences have led to widely-applied advances in computer science, especially string searching algorithms, machine learning and database theory.[110] String searching or matching algorithms, which find an occurrence of a sequence of letters inside a larger sequence of letters, were developed to search for specific sequences of nucleotides.[111] In other applications such as text editors, even simple algorithms for this problem usually suffice, but DNA sequences cause these algorithms to exhibit near-worst-case behaviour due to their small number of distinct characters. The related problem of sequence alignment aims to identify homologous sequences and locate the specific mutations that make them distinct. These techniques, especially multiple sequence alignment, are used in studying phylogenetic relationships and protein function.[112] 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 the characteristic patterns associated with protein- or RNA-coding genes can be identified by gene finding algorithms, which allow researchers to predict the presence of particular gene products in an organism even before they have been isolated experimentally.[113]

### DNA nanotechnologyEdit

Further information: DNA nanotechnology

DNA nanotechnology uses the unique molecular recognition properties of DNA and other nucleic acids to create self-assembling branched DNA complexes with useful properties. DNA is thus used as a structural material rather than as a carrier of biological information. This has led to the creation of two-dimensional periodic lattices (both tile-based as well as using the "DNA origami" method) as well as three-dimensional structures in the shapes of polyhedra. Nanomechanical devices and algorithmic self-assembly have also been demonstrated, and these DNA structures have been used to template the arrangement of other molecules such as gold nanoparticles and streptavidin proteins.

### History and anthropologyEdit

Further information: Phylogenetics and Genetic genealogy

Because DNA collects mutations over time, which are then inherited, it contains historical information and by comparing DNA sequences, geneticists can infer the evolutionary history of organisms, their phylogeny.[114] This field of phylogenetics is a powerful tool in evolutionary biology. If DNA sequences within a species are compared, population geneticists can learn the history of particular populations. This can be used in studies ranging from ecological genetics to anthropology; for example, DNA evidence is being used to try to identify the Ten Lost Tribes of Israel.[115][116]

DNA has also been used to look at modern family relationships, such as establishing family relationships between the descendants of Sally Hemings and Thomas Jefferson. This usage is closely related to the use of DNA in criminal investigations detailed above. Indeed, some criminal investigations have been solved when DNA from crime scenes has matched relatives of the guilty individual.[117]

## History of DNA researchEdit

Further information: History of molecular biology

DNA was first isolated by the Swiss physician 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".[118] In 1919 this discovery was followed by Phoebus Levene's identification of the base, sugar and phosphate nucleotide unit.[119] 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.[120]

In 1928, Frederick Griffith 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.[121] This system provided the first clear suggestion that DNA carried genetic information, when Oswald Avery, along with coworkers Colin MacLeod and Maclyn McCarty, identified DNA as the transforming principle in 1943.[122] DNA's role in heredity was confirmed in 1952, when Alfred Hershey and Martha Chase in the Hershey-Chase experiment showed that DNA is the genetic material of the T2 phage.[123]

In 1953, based on X-ray diffraction images[124] taken by Rosalind Franklin and the information that the bases were paired, James D. Watson and Francis Crick suggested[124] what is now accepted as the first accurate model of DNA structure in the journal Nature.[5] Experimental evidence for Watson and Crick's model were published in a series of five articles in the same issue of Nature.[125] Of these, Franklin and Raymond Gosling's paper was the first publication of X-ray diffraction data that supported the Watson and Crick model,[126][127] this issue also contained an article on DNA structure by Maurice Wilkins and his colleagues.[128] In 1962, after Franklin's death, Watson, Crick, and Wilkins jointly received the Nobel Prize in Physiology or Medicine.[129] However, debate continues on who should receive credit for the discovery.[130]

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".[131] Final confirmation of the replication mechanism that was implied by the double-helical structure followed in 1958 through the Meselson-Stahl experiment.[132] 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.[133] These findings represent the birth of molecular biology.

## ReferencesEdit

1. 1.0 1.1 Alberts, Bruce; Alexander Johnson, Julian Lewis, Martin Raff, Keith Roberts, and Peter Walters (2002). Molecular Biology of the Cell; Fourth Edition, New York and London: Garland Science.
2. Butler, John M. (2001). Forensic DNA Typing, Elsevier.pp. 14–15.
3. Mandelkern M, Elias J, Eden D, Crothers D (1981). The dimensions of DNA in solution. J Mol Biol 152 (1): 153–61.
4. Gregory S, et al. (2006). The DNA sequence and biological annotation of human chromosome 1. Nature 441 (7091): 315–21.
5. 5.0 5.1 Watson J, Crick F (1953). Molecular structure of nucleic acids; a structure for deoxyribose nucleic acid. Nature 171 (4356): 737–8.
6. 6.0 6.1 6.2 Berg J., Tymoczko J. and Stryer L. (2002) Biochemistry. W. H. Freeman and Company ISBN 0-7167-4955-6
7. Abbreviations and Symbols for Nucleic Acids, Polynucleotides and their Constituents IUPAC-IUB Commission on Biochemical Nomenclature (CBN), Accessed 03 Jan 2006
8. 8.0 8.1 Ghosh A, Bansal M (2003). A glossary of DNA structures from A to Z. Acta Crystallogr D Biol Crystallogr 59 (Pt 4): 620–6.
9. Created from PDB 1D65
10. Wing R, Drew H, Takano T, Broka C, Tanaka S, Itakura K, Dickerson R (1980). Crystal structure analysis of a complete turn of B-DNA. Nature 287 (5784): 755–8.
11. Pabo C, Sauer R (1984). Protein-DNA recognition. Annu Rev Biochem 53: 293–321.
12. Clausen-Schaumann H, Rief M, Tolksdorf C, Gaub H (2000). Mechanical stability of single DNA molecules. Biophys J 78 (4): 1997–2007.
13. Peter Yakovchuk, Ekaterina Protozanova and Maxim D. Frank-Kamenetskii. Base-stacking and base-pairing contributions into thermal stability of the DNA double helix. Nucleic Acids Research 2006 34(2):564-574; doi:10.1093/nar/gkj454 PMID 16449200
14. Chalikian T, Völker J, Plum G, Breslauer K (1999). A more unified picture for the thermodynamics of nucleic acid duplex melting: a characterization by calorimetric and volumetric techniques. Proc Natl Acad Sci USA 96 (14): 7853–8.
15. deHaseth P, Helmann J (1995). Open complex formation by Escherichia coli RNA polymerase: the mechanism of polymerase-induced strand separation of double helical DNA. Mol Microbiol 16 (5): 817–24.
16. Isaksson J, Acharya S, Barman J, Cheruku P, Chattopadhyaya J (2004). Single-stranded adenine-rich DNA and RNA retain structural characteristics of their respective double-stranded conformations and show directional differences in stacking pattern. Biochemistry 43 (51): 15996–6010.
17. Designation of the two strands of DNA JCBN/NC-IUB Newsletter 1989, Accessed 07 May 2008
18. Hüttenhofer A, Schattner P, Polacek N (2005). Non-coding RNAs: hope or hype?. Trends Genet 21 (5): 289–97.
19. Munroe S (2004). Diversity of antisense regulation in eukaryotes: multiple mechanisms, emerging patterns. J Cell Biochem 93 (4): 664–71.
20. Makalowska I, Lin C, Makalowski W (2005). Overlapping genes in vertebrate genomes. Comput Biol Chem 29 (1): 1–12.
21. Johnson Z, Chisholm S (2004). Properties of overlapping genes are conserved across microbial genomes. Genome Res 14 (11): 2268–72.
22. Lamb R, Horvath C (1991). Diversity of coding strategies in influenza viruses. Trends Genet 7 (8): 261–6.
23. Benham C, Mielke S (2005). DNA mechanics. Annu Rev Biomed Eng 7: 21–53.
24. 24.0 24.1 Champoux J (2001). DNA topoisomerases: structure, function, and mechanism. Annu Rev Biochem 70: 369–413.
25. 25.0 25.1 Wang J (2002). Cellular roles of DNA topoisomerases: a molecular perspective. Nat Rev Mol Cell Biol 3 (6): 430–40.
26. Basu H, Feuerstein B, Zarling D, Shafer R, Marton L (1988). Recognition of Z-RNA and Z-DNA determinants by polyamines in solution: experimental and theoretical studies. J Biomol Struct Dyn 6 (2): 299–309.
27. Leslie AG, Arnott S, Chandrasekaran R, Ratliff RL (1980). Polymorphism of DNA double helices. J. Mol. Biol. 143 (1): 49–72.
28. Wahl M, Sundaralingam M (1997). Crystal structures of A-DNA duplexes. Biopolymers 44 (1): 45–63.
29. Lu XJ, Shakked Z, Olson WK (2000). A-form conformational motifs in ligand-bound DNA structures. J. Mol. Biol. 300 (4): 819–40.
30. Rothenburg S, Koch-Nolte F, Haag F (2001). DNA methylation and Z-DNA formation as mediators of quantitative differences in the expression of alleles. Immunol Rev 184: 286–98.
31. Oh D, Kim Y, Rich A (2002). Z-DNA-binding proteins can act as potent effectors of gene expression in vivo. Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16666–71.
32. Created from NDB UD0017
33. 33.0 33.1 Greider C, Blackburn E (1985). Identification of a specific telomere terminal transferase activity in Tetrahymena extracts. Cell 43 (2 Pt 1): 405–13.
34. 34.0 34.1 34.2 Nugent C, Lundblad V (1998). The telomerase reverse transcriptase: components and regulation. Genes Dev 12 (8): 1073–85.
35. Wright W, Tesmer V, Huffman K, Levene S, Shay J (1997). Normal human chromosomes have long G-rich telomeric overhangs at one end. Genes Dev 11 (21): 2801–9.
36. 36.0 36.1 Burge S, Parkinson G, Hazel P, Todd A, Neidle S (2006). Quadruplex DNA: sequence, topology and structure. Nucleic Acids Res 34 (19): 5402–15.
37. Parkinson G, Lee M, Neidle S (2002). Crystal structure of parallel quadruplexes from human telomeric DNA. Nature 417 (6891): 876–80.
38. Griffith J, Comeau L, Rosenfield S, Stansel R, Bianchi A, Moss H, de Lange T (1999). Mammalian telomeres end in a large duplex loop. Cell 97 (4): 503–14.
39. Klose R, Bird A (2006). Genomic DNA methylation: the mark and its mediators. Trends Biochem Sci 31 (2): 89–97.
40. Bird A (2002). DNA methylation patterns and epigenetic memory. Genes Dev 16 (1): 6–21.
41. Walsh C, Xu G (2006). Cytosine methylation and DNA repair. Curr Top Microbiol Immunol 301: 283–315.
42. Ratel D, Ravanat J, Berger F, Wion D (2006). N6-methyladenine: the other methylated base of DNA. Bioessays 28 (3): 309–15.
43. Gommers-Ampt J, Van Leeuwen F, de Beer A, Vliegenthart J, Dizdaroglu M, Kowalak J, Crain P, Borst P (1993). beta-D-glucosyl-hydroxymethyluracil: a novel modified base present in the DNA of the parasitic protozoan T. brucei. Cell 75 (6): 1129–36.
44. Created from PDB 1JDG
45. Douki T, Reynaud-Angelin A, Cadet J, Sage E (2003). Bipyrimidine photoproducts rather than oxidative lesions are the main type of DNA damage involved in the genotoxic effect of solar UVA radiation. Biochemistry 42 (30): 9221–6.,
46. Cadet J, Delatour T, Douki T, Gasparutto D, Pouget J, Ravanat J, Sauvaigo S (1999). Hydroxyl radicals and DNA base damage. Mutat Res 424 (1–2): 9–21.
47. Shigenaga M, Gimeno C, Ames B (1989). Urinary 8-hydroxy-2′-deoxyguanosine as a biological marker of in vivo oxidative DNA damage. Proc Natl Acad Sci USA 86 (24): 9697–701.
48. Cathcart R, Schwiers E, Saul R, Ames B (1984). Thymine glycol and thymidine glycol in human and rat urine: a possible assay for oxidative DNA damage. Proc Natl Acad Sci USA 81 (18): 5633–7.
49. Valerie K, Povirk L (2003). Regulation and mechanisms of mammalian double-strand break repair. Oncogene 22 (37): 5792–812.
50. Ferguson L, Denny W (1991). The genetic toxicology of acridines. Mutat Res 258 (2): 123–60.
51. Jeffrey A (1985). DNA modification by chemical carcinogens. Pharmacol Ther 28 (2): 237–72.
52. Stephens T, Bunde C, Fillmore B (2000). Mechanism of action in thalidomide teratogenesis. Biochem Pharmacol 59 (12): 1489–99.
53. Braña M, Cacho M, Gradillas A, de Pascual-Teresa B, Ramos A (2001). Intercalators as anticancer drugs. Curr Pharm Des 7 (17): 1745–80.
54. Venter J, et al. (2001). The sequence of the human genome. Science 291 (5507): 1304–51.
55. Thanbichler M, Wang S, Shapiro L (2005). The bacterial nucleoid: a highly organized and dynamic structure. J Cell Biochem 96 (3): 506–21.
56. Wolfsberg T, McEntyre J, Schuler G (2001). Guide to the draft human genome. Nature 409 (6822): 824–6.
57. Gregory T (2005). The C-value enigma in plants and animals: a review of parallels and an appeal for partnership. Ann Bot (Lond) 95 (1): 133–46.
58. The ENCODE Project Consortium (2007). Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature 447 (7146): 799–816.
59. Created from PDB 1MSW
60. Pidoux A, Allshire R (2005). The role of heterochromatin in centromere function. Philos Trans R Soc Lond B Biol Sci 360 (1455): 569–79.
61. Harrison P, Hegyi H, Balasubramanian S, Luscombe N, Bertone P, Echols N, Johnson T, Gerstein M (2002). Molecular fossils in the human genome: identification and analysis of the pseudogenes in chromosomes 21 and 22. Genome Res 12 (2): 272–80.
62. Harrison P, Gerstein M (2002). Studying genomes through the aeons: protein families, pseudogenes and proteome evolution. J Mol Biol 318 (5): 1155–74.
63. Albà M (2001). Replicative DNA polymerases. Genome Biol 2 (1): REVIEWS3002.
64. Sandman K, Pereira S, Reeve J (1998). Diversity of prokaryotic chromosomal proteins and the origin of the nucleosome. Cell Mol Life Sci 54 (12): 1350–64.
65. Dame RT (2005). The role of nucleoid-associated proteins in the organization and compaction of bacterial chromatin. Mol. Microbiol. 56 (4): 858–70.
66. Luger K, Mäder A, Richmond R, Sargent D, Richmond T (1997). Crystal structure of the nucleosome core particle at 2.8 A resolution. Nature 389 (6648): 251–60.
67. Jenuwein T, Allis C (2001). Translating the histone code. Science 293 (5532): 1074–80.
68. Ito T. Nucleosome assembly and remodelling. Curr Top Microbiol Immunol 274: 1–22.
69. Thomas J (2001). HMG1 and 2: architectural DNA-binding proteins. Biochem Soc Trans 29 (Pt 4): 395–401.
70. Grosschedl R, Giese K, Pagel J (1994). HMG domain proteins: architectural elements in the assembly of nucleoprotein structures. Trends Genet 10 (3): 94–100.
71. Iftode C, Daniely Y, Borowiec J (1999). Replication protein A (RPA): the eukaryotic SSB. Crit Rev Biochem Mol Biol 34 (3): 141–80.
72. Created from PDB 1LMB
73. Myers L, Kornberg R (2000). Mediator of transcriptional regulation. Annu Rev Biochem 69: 729–49.
74. Spiegelman B, Heinrich R (2004). Biological control through regulated transcriptional coactivators. Cell 119 (2): 157–67.
75. Li Z, Van Calcar S, Qu C, Cavenee W, Zhang M, Ren B (2003). A global transcriptional regulatory role for c-Myc in Burkitt's lymphoma cells. Proc Natl Acad Sci USA 100 (14): 8164–9.
76. Pabo C, Sauer R (1984). Protein-DNA recognition. Annu Rev Biochem 53: 293–321.
77. Created from PDB 1RVA
78. Bickle T, Krüger D (1993). Biology of DNA restriction. Microbiol Rev 57 (2): 434–50.
79. 79.0 79.1 Doherty A, Suh S (2000). Structural and mechanistic conservation in DNA ligases. Nucleic Acids Res 28 (21): 4051–8.
80. Schoeffler A, Berger J (2005). Recent advances in understanding structure-function relationships in the type II topoisomerase mechanism. Biochem Soc Trans 33 (Pt 6): 1465–70.
81. Tuteja N, Tuteja R (2004). Unraveling DNA helicases. Motif, structure, mechanism and function. Eur J Biochem 271 (10): 1849–63.
82. 82.0 82.1 Joyce C, Steitz T (1995). Polymerase structures and function: variations on a theme?. J Bacteriol 177 (22): 6321–9.
83. Hubscher U, Maga G, Spadari S (2002). Eukaryotic DNA polymerases. Annu Rev Biochem 71: 133–63.
84. Johnson A, O'Donnell M (2005). Cellular DNA replicases: components and dynamics at the replication fork. Annu Rev Biochem 74: 283–315.
85. Tarrago-Litvak L, Andréola M, Nevinsky G, Sarih-Cottin L, Litvak S (1994). The reverse transcriptase of HIV-1: from enzymology to therapeutic intervention. Faseb J 8 (8): 497–503.
86. Martinez E (2002). Multi-protein complexes in eukaryotic gene transcription. Plant Mol Biol 50 (6): 925–47.
87. Created from PDB 1M6G
88. Cremer T, Cremer C (2001). Chromosome territories, nuclear architecture and gene regulation in mammalian cells. Nat Rev Genet 2 (4): 292–301.
89. Pál C, Papp B, Lercher M (2006). An integrated view of protein evolution. Nat Rev Genet 7 (5): 337–48.
90. O'Driscoll M, Jeggo P (2006). The role of double-strand break repair - insights from human genetics. Nat Rev Genet 7 (1): 45–54.
91. Vispé S, Defais M (1997). Mammalian Rad51 protein: a RecA homologue with pleiotropic functions. Biochimie 79 (9-10): 587–92.
92. Neale MJ, Keeney S (2006). Clarifying the mechanics of DNA strand exchange in meiotic recombination. Nature 442 (7099): 153–8.
93. Dickman M, Ingleston S, Sedelnikova S, Rafferty J, Lloyd R, Grasby J, Hornby D (2002). The RuvABC resolvasome. Eur J Biochem 269 (22): 5492–501.
94. Orgel L. Prebiotic chemistry and the origin of the RNA world. Crit Rev Biochem Mol Biol 39 (2): 99–123.
95. Davenport R (2001). Ribozymes. Making copies in the RNA world. Science 292 (5520): 1278.
96. Szathmáry E (1992). What is the optimum size for the genetic alphabet?. Proc Natl Acad Sci USA 89 (7): 2614–8.
97. Lindahl T (1993). Instability and decay of the primary structure of DNA. Nature 362 (6422): 709–15.
98. Vreeland R, Rosenzweig W, Powers D (2000). Isolation of a 250 million-year-old halotolerant bacterium from a primary salt crystal. Nature 407 (6806): 897–900.
99. Hebsgaard M, Phillips M, Willerslev E (2005). Geologically ancient DNA: fact or artefact?. Trends Microbiol 13 (5): 212–20.
100. Nickle D, Learn G, Rain M, Mullins J, Mittler J (2002). Curiously modern DNA for a "250 million-year-old" bacterium. J Mol Evol 54 (1): 134–7.
101. Goff SP, Berg P (1976). Construction of hybrid viruses containing SV40 and lambda phage DNA segments and their propagation in cultured monkey cells. Cell 9 (4 PT 2): 695–705.
102. Houdebine L. Transgenic animal models in biomedical research. Methods Mol Biol 360: 163–202.
103. Daniell H, Dhingra A (2002). Multigene engineering: dawn of an exciting new era in biotechnology. Curr Opin Biotechnol 13 (2): 136–41.
104. Job D (2002). Plant biotechnology in agriculture. Biochimie 84 (11): 1105–10.
105. Collins A, Morton N (1994). Likelihood ratios for DNA identification. Proc Natl Acad Sci USA 91 (13): 6007–11.
106. Weir B, Triggs C, Starling L, Stowell L, Walsh K, Buckleton J (1997). Interpreting DNA mixtures. J Forensic Sci 42 (2): 213–22.
107. Jeffreys A, Wilson V, Thein S (1985). Individual-specific 'fingerprints' of human DNA. Nature 316 (6023): 76–9.
108. Colin Pitchfork — first murder conviction on DNA evidence also clears the prime suspect Forensic Science Service Accessed 23 Dec 2006
109. (2006). DNA Identification in Mass Fatality Incidents. National Institute of Justice.
110. Baldi, Pierre. Brunak, Soren (2001). Bioinformatics: The Machine Learning Approach, MIT Press.
111. Gusfield, Dan. Algorithms on Strings, Trees, and Sequences: Computer Science and Computational Biology. Cambridge University Press, 15 January 1997. ISBN 978-0-521-58519-4.
112. Sjölander K (2004). Phylogenomic inference of protein molecular function: advances and challenges. Bioinformatics 20 (2): 170–9.
113. Mount DM (2004). Bioinformatics: Sequence and Genome Analysis, 2, Cold Spring Harbor Laboratory Press.
114. Wray G (2002). Dating branches on the tree of life using DNA. Genome Biol 3 (1): REVIEWS0001.
115. Lost Tribes of Israel, NOVA, PBS airdate: 22 February 2000. Transcript available from PBS.org, (last accessed on 4 March 2006)
116. Kleiman, Yaakov. "The Cohanim/DNA Connection: The fascinating story of how DNA studies confirm an ancient biblical tradition". aish.com (January 13, 2000). Accessed 4 March 2006.
117. Bhattacharya, Shaoni. "Killer convicted thanks to relative's DNA". newscientist.com (20 April 2004). Accessed 22 Dec 06
118. Dahm R (2005). Friedrich Miescher and the discovery of DNA. Dev Biol 278 (2): 274–88.
119. Levene P, (1919). The structure of yeast nucleic acid. J Biol Chem 40 (2): 415–24.
120. Astbury W, (1947). Nucleic acid. Symp. SOC. Exp. Bbl 1 (66).
121. Lorenz MG, Wackernagel W (1994). Bacterial gene transfer by natural genetic transformation in the environment. Microbiol. Rev. 58 (3): 563–602.
122. Avery O, MacLeod C, McCarty M (1944). 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. J Exp Med 79 (2): 137–158.
123. Hershey A, Chase M (1952). Independent functions of viral protein and nucleic acid in growth of bacteriophage. J Gen Physiol 36 (1): 39–56.
124. 124.0 124.1 Watson J.D. and Crick F.H.C. (1953). A Structure for Deoxyribose Nucleic Acid. Nature 171: 737–738.
125. Nature Archives Double Helix of DNA: 50 Years
126. Franklin, Rosalind (1953). Molecular Configuration in Sodium Thymonucleate. Franklin R. and Gosling R.G. Nature 171: 740–741.
127. Original X-ray diffraction image
128. Wilkins M.H.F., A.R. Stokes A.R. & Wilson, H.R. (1953). Molecular Structure of Deoxypentose Nucleic Acids. Nature 171: 738–740.
129. The Nobel Prize in Physiology or Medicine 1962 Nobelprize .org Accessed 22 Dec 06
130. Brenda Maddox (23 January 2003). The double helix and the 'wronged heroine'. Nature 421: 407–408.
131. Crick, F.H.C. On degenerate templates and the adaptor hypothesis (PDF). genome.wellcome.ac.uk (Lecture, 1955). Accessed 22 Dec 2006
132. Meselson M, Stahl F (1958). The replication of DNA in Escherichia coli. Proc Natl Acad Sci USA 44 (7): 671–82.
133. The Nobel Prize in Physiology or Medicine 1968 Nobelprize.org Accessed 22 Dec 06