Non-helical models of DNA structure

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Watson-Crick plectonemic structure
Example of non-helical (paranemic) structure
Left: the Watson–Crick double helix, which is the currently accepted model for the structure of nucleic acids. Right: one example of a side by side, non-helical model for nucleic acid structure.

In the history of molecular biology, non-helical or "side-by-side" models of DNA were proposed in the 1970s as a challenge to the standard double-helical model. The non-helical models attempted to solve problems relating to the topology of circular DNA chromosomes during replication. These theories were briefly considered seriously as a minority viewpoint,[1] but they were later largely rejected due to X-ray crystallography of DNA duplexes and later the nucleosome core particle, as well as the discovery of topoisomerases, and these non-double-helical models are not currently accepted by the mainstream scientific community.[2]


Plectonemic circular strands
Paranemic circular strands
Top: A rope model of a circularized plectonemic (helical) duplex, showing that when one cannot separate the strands without breaking at least one of them, a tangled knot results. Bottom: A rope model of a circularized paranemic (non-helical) duplex, the strands of which can be easily separated.

The strands of a helical DNA duplex, if covalently closed into a circular structure, are topologically linked, and thus cannot be separated without breaking one or both strands. This sort of structure is referred to as "plectonemic". In circular DNA replication, these twists must be removed for the daughter strands to separate. In contrast, the strands of a non-helical DNA duplex would be topologically non-linked, and can be separated without strand breakage. This sort of structure is referred to as "paranemic".[3][4]

Note that the term "non-helical" refers to net helicity - there can be no helical twist at all, as in the figure at the top of this article, or there could be an equal number of right-handed and left-handed twists, as in the Rodley structure below. The abbreviation "TN", to be used to refer to any DNA structure whose strands are topologically non-linked, has been proposed.[3]

Historical background[edit]

Proposal of Watson–Crick helical structure[edit]

The double-helix model of DNA structure was first published in the journal Nature by James D. Watson and Francis Crick in 1953[5] with further details in 1954.[6]) Their work was based upon the crucial X-ray diffraction image of DNA - labeled as "Photo 51" - from Rosalind Franklin in 1952,[7] followed by her more highly clarified DNA image with Raymond Gosling,[8][9] Maurice Wilkins, Alexander Stokes, and Herbert Wilson,[10] as well as base-pairing chemical and biochemical information by Erwin Chargaff.[11][12] Wilkins and colleagues also reported on X-ray patterns of the state of in vivo B-DNA in partially oriented salmon sperm heads.[10] Crick, Wilkins, and Watson each received one-third of the 1962 Nobel Prize in Physiology or Medicine for their contributions to this discovery.[13] Franklin, whose breakthrough X-ray diffraction data was used to formulate the DNA structure, died in 1958, and thus was ineligible to be nominated for a Nobel Prize.

Discovery of circular DNA[edit]

In 1963, John Cairns published autoradiographs of the E. coli chromosome, showing that it was a single circular molecule that is replicated at a moving locus - the "replication fork" - at which both new DNA strands are being synthesized.[14] Cairns, at that time, recognized a topological problem in that the helical twists between the daughter strands would have to be removed if the strands are to separate during cell replication. He proposed that the twists were unwound by means of a hypothetical "swivel" around which the chromosome would be free to rotate as necessary for the un-winding and re-winding operations.[15] However, such a structure would have to have about 400,000 helical twists in the Watson–Crick model, each of which would have to be removed in as little as 20 minutes, if the strands are to separate during cell replication. This leads to the apparent need of the chromosome - or at least some part of it - to be spinning at speeds up to 6900–9000 rpm throughout the life of the bacterial cell.[16]

Rodley non-helical structure proposed[edit]

A video of the Rodley side-by-side structure

In 1976, Gordon Rodley and his co-workers published the first non-helical DNA structure, which they named the "side-by-side" (SBS) structure.[18] A similar model was published a few months later by Sasisekharan and his associates.[19][20] The SBS structure was hypothetical, and was not based primarily upon physical evidence. It was created to provide a theoretical solution to the angular momentum problem in DNA replication, which Rodley believed to be otherwise unsolvable.

The SBS structure is a modification of the original Watson-Crick structure where, instead of one fully right-handed helical twist every 10 base pairs, there is only a half-twist of 5 base pairs’ length, followed immediately by a half-twist in the opposite direction (that is, a left-handed half-twist, also of 5 base pairs’ length). This alternating pattern of right- and left-handed half-twists is repeated throughout the length of the chromosome which, topologically speaking, would have no net twists. Such a chromosome does not need to either spin or unwind during replication. Rodley in later published work makes it clear that it was not the intention of his team that the model utilized alternating half turns of opposite helical sense, but lengths of DNA having alternating helical senses deployed in the available space along the DNA molecule that would not exactly be half turns.[21]

Experimental studies of circular DNA structure[edit]

One key observation in support of a double-helical structure is that the individual single strands of small circular viral and plasmid DNA are inseparable under the usual types of denaturation conditions, supporting a plectonemic, i.e., twisted structure whose strands are topologically locked together. While human and bacterial chromosomes are far too large to isolate intact, but rather break into innumerable small fragments when extracted from their respective cells, there exist many species of small viral and plasmid chromosomes which because of their small sizes are stable in solution, and remain intact even with vigorous handling. Early studies quickly revealed that the strands of duplex circular chromosomes do not separate when subjected to conditions which readily denature linear DNA.[22] For example, if calf thymus DNA (a heterogeneous collection of linear fragments) is merely boiled, the strands separate, and when slowly cooled, they re-anneal. In contrast, when the circular chromosomes of such organisms as the replicative form (RF) of the bacteriophage φX174, or the mammalian virus polyoma, are boiled, nothing at all happens to the native structure - they are completely resistant to thermal denaturation. Without a doubt, the single most skepticism-inspiring aspect of non-helical DNA theory was the failure of the strands of circular chromosomes to separate under conditions where the strands of linear DNA would readily do so. This was generally regarded as evidence that the strands were plectonemically wound together (i.e., topologically linked).

The publication of the Rodley structure produced a small but significant ripple of interest in the molecular biological community. However, the level of interest was sufficiently high so that Crick - by that time one of the world’s most influential scientists - publicly suggested that the SBS structure (whose existence he doubted) should be laid to rest by intentionally creating it. Then, he reasoned, its properties could be ascertained, and then shown to be abnormal with respect to the known properties of native DNA.[23] An investigation by Stettler et al. followed closely on the heels of the Crick suggestion. They isolated the intact circular single strands of a circular duplex viral chromosome and then re-annealed them, giving a product they declared to be a "base-paired circular duplex with no net helical twist". If so, this would in fact be the Rodley "side-by-side" structure. They introduced a new terminology for this product, calling it "Form V" (extending the nomenclature of Forms I–IV used in sedimentation studies of DNA), and then went on to demonstrate that its electrophoretic mobility was clearly different from that of the native chromosome.[24]

Drawing illustrating D-loops forming on the sense strand of DNA isolated during transcription of RNA.

The results of this investigation were not accepted by some authors, who agreed that it was established satisfactorily that "Form V" is different from native DNA, but did not establish that "Form V" has the SBS structure. While the strands of native circular DNA are known not to be separable under common denaturing conditions, in 1996, following his earlier theoretical studies in 1969, Tai Te Wu reported having found conditions under which fully intact single strands of two different circular duplex plasmids could be separated.[25] Wu believed that, because these plasmids have D-loops with DNA–RNA duplexes from RNA transcription only on their sense side, and since DNA–RNA interactions are stronger than DNA–DNA interactions,[26] the sense and anti-sense strands would thus have different electrophoretic mobilities. He employed a very low voltage, so that the electrophoresis required 48 hours to go to completion. DNA sequencing then indicated that each of the two bands were enriched in one of the two strands of the chromosome. Separately, the Stetter et al. experiment was revisited in 2009 by Youcheng Xu, who noted that brief re-annealing times (i.e. 20–30 minutes) resulted in anomalous structures which did not co-migrate with routinely prepared DNA topoisomers, while prolonged re-annealing times (in his case, 72 hours at 4º) resulted in structures which did co-migrate with the topoisomers, suggesting normal base-pairing. They interpreted their data as supporting the possibility that the two strands inside the native DNA double helix are winding ambidextrously rather than plectonemically, with left-handed and right-handed regions coexisting in a zero linking number topoisomer.[27][28]

Other experimental developments[edit]

The discovery of topoisomerases, enzymes that can change the linking number of circular nucleic acids and thus "unwind" the replicating bacterial chomosome, was largely seen by the mainstream scientific community to satisfy the topological objection to the Watson–Crick helical structure. The later X-ray crystallography data for the nucleosome, which showed a helical DNA structure wrapped around the protein nucleosome core particle, was considered to provide further affirmation for the existence of the helical structure in vivo. Non-double-helical models are not currently accepted by the mainstream scientific community.[2]

Enzymes capable of unwinding and rewinding DNA helical twists, namely topoisomerases and gyrases, are essential for life, and necessary for DNA replication in various in vitro synthesis systems.


  1. ^ Stokes, T. D. (1982). "The double helix and the warped zipper—an exemplary tale". Social Studies of Science 12 (2): 207–240. doi:10.1177/030631282012002002. 
  2. ^ a b Gautham, N. (25 May 2004). "Response to "Variety in DNA secondary structure"". Current Science 86 (10): 1352–1353. Retrieved 28 November 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." 
  3. ^ a b Biegeleisen K (May 2002). "Topologically non-linked circular duplex DNA". Bull. Math. Biol. 64 (3): 589–609. doi:10.1006/bulm.2002.0288. PMID 12094410. 
  4. ^ Delmonte, C. S.; Mann, L. R. B. "Variety in DNA secondary structure". Current Science 85: 1564–1570. 
  5. ^ James D. Watson and Francis Crick (1953). "A structure for deoxyribose nucleic acid". Nature 171 (4356): 737–8. Bibcode:1953Natur.171..737W. doi:10.1038/171737a0. PMID 13054692. 
  6. ^ Crick, Francis, and James D. Watson (1954). "The Complementary Structure of Deoxyribonucleic Acid". Proceedings of the Royal Society of London. 223, Series A: 80–96. 
  7. ^ "Secret of Photo 51". NOVA. PBS. 
  8. ^
  9. ^ The Structure of the DNA Molecule
  10. ^ a b Wilkins MHF, Stokes AR, Wilson HR (1953). "Molecular Structure of Deoxypentose Nucleic Acids" (PDF). Nature 171 (4356): 738–740. Bibcode:1953Natur.171..738W. doi:10.1038/171738a0. PMID 13054693. 
  11. ^ Magasanik B, Vischer E, Doniger R, Elson D, Chargaff E (1950). "The separation and estimation of ribonucleotides in minute quantities". J Biol Chem 186 (1): 37–50. PMID 14778802. 
  12. ^ Chargaff E (1950). "Chemical specificity of nucleic acids and mechanism of their enzymatic degradation". Experientia 6 (6): 201–209. doi:10.1007/BF02173653. PMID 15421335. 
  13. ^ "Nobel Prize - List of All Nobel Laureates". 
  14. ^ Cairns, J. (March 1963). "The bacterial chromosome and its manner of replication as seen by autoradiography". J. Mol. Biol. 6: 208–13. doi:10.1016/s0022-2836(63)80070-4. PMID 14017761. 
  15. ^ Cairns J (1963). "The chromosome of Escherichia coli". Cold Spring Harbor Symp Quant Biol 28: 43–46. doi:10.1101/SQB.1963.028.01.011. 
  16. ^ Górski, F. (1975). "Critical review of the mechanisms separating the strands of DNA double helices during cell division". Folia Biologica (Krakow) 23 (1): 81–111. PMID 1157978. 
  17. ^ Biegeleisen, K., 2005. Rodley Side-By-Side Structure. Protein Data Bank,, accession number 2AW8.
  18. ^ Rodley GA, Scobie RS, Bates RH, Lewitt RM (September 1976). "A possible conformation for double-stranded polynucleotides". Proc. Natl. Acad. Sci. U.S.A. 73 (9): 2959–63. Bibcode:1976PNAS...73.2959R. doi:10.1073/pnas.73.9.2959. PMC 430891. PMID 1067594. 
  19. ^ Sasisekharan V, Pattabiraman N & Gupta G (1976). Curr Sci 45, 779-783. Current Science home page: Free PDF download at
  20. ^ Sasisekharan V, Pattabiraman N, Gupta G (September 1978). "Some implications of an alternative structure for DNA". Proc. Natl. Acad. Sci. U.S.A. 75 (9): 4092–6. Bibcode:1978PNAS...75.4092S. doi:10.1073/pnas.75.9.4092. PMC 336057. PMID 279899. 
  21. ^ Rodley, G. A. (1995). "Reconsideration of some results for linear and circular DNA". Journal of Biosciences 20 (2): 245–257. doi:10.1007/BF02703272.  edit
  22. ^ Vinograd J, Lebowitz J, Radloff R, Watson R, Laipis P (May 1965). "The twisted circular form of polyoma viral DNA". Proc. Natl. Acad. Sci. U.S.A. 53 (5): 1104–11. Bibcode:1965PNAS...53.1104V. doi:10.1073/pnas.53.5.1104. PMC 301380. PMID 4287964. 
  23. ^ Crick FH, Wang JC, Bauer WR (April 1979). "Is DNA really a double helix?". J. Mol. Biol. 129 (3): 449–57. doi:10.1016/0022-2836(79)90506-0. PMID 458852. 
  24. ^ Stettler UH, Weber H, Koller T, Weissmann C (June 1979). "Preparation and characterization of form V DNA, the duplex DNA resulting from association of complementary, circular single-stranded DNA". J. Mol. Biol. 131 (1): 21–40. doi:10.1016/0022-2836(79)90299-7. PMID 490644. 
  25. ^ Wu R, Wu T (November 1996). "A novel intact circular dsDNA supercoil". Bull. Math. Biol. 58 (6): 1171–85. doi:10.1007/BF02458388. PMID 8953261. 
  26. ^ Casey J, Davidson N (1977). "Rates of formation and thermal stabilities of RNA:DNA and DNA:DNA duplexes at high concentrations of formamide". Nucleic Acids Res. 4 (5): 1539–52. doi:10.1093/nar/4.5.1539. PMC 343772. PMID 19730. 
  27. ^ Xu YC (February 2009). "Finding of a zero linking number topoisomer". Biochim. Biophys. Acta 1790 (2): 126–33. doi:10.1016/j.bbagen.2008.10.012. PMID 19063942. 
  28. ^ Xu YC. Replication demands an amendment of the double helix. Ed by H. Selihmann in DNA replication-current advances. Intech . 2011; p, 29-56