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. 1995 Nov;69(5):2033–2043. doi: 10.1016/S0006-3495(95)80073-1

Conformational transitions of alternating purine-pyrimidine DNAs in perchlorate ethanol solutions.

M Vorlícková 1
PMCID: PMC1236436  PMID: 8580346

Abstract

Conformational transitions of poly(dA-dC).poly(dG-dT), poly(dA-dT).poly(dA-dT), and other alternating purine-pyrimidine DNAs were studied in aqueous ethanol solutions containing molar concentrations of sodium perchlorate, which is a novel solvent stabilizing non-B duplexes of DNA. Using CD and UV absorption spectroscopies, we show that this solvent unstacks bases and unwinds the B-forms of the DNAs to transform them into the A-form or Z-form. In the absence of divalent cations poly(dA-dC).poly(dG-dT) can adopt both of these conformations. Its transition into the Z-form is induced at higher salt and lower ethanol concentrations, and at higher temperatures than the transition into the A-form. Submillimolar concentrations of NiCl2 induce a highly cooperative and slow A-Z transition or Z-Z' transition, which is fast and displays low cooperativity. Poly(dA-dT).poly(dA-dT) easily isomerizes into the A-form in perchlorate-ethanol solutions, whereas high perchlorate concentrations denature the polynucleotide, which then cannot adopt the Z-form. At low temperatures, however, NiCl2 also cooperatively induces the Z'-form in poly(dA-dT).poly(dA-dT). Poly(dI-dC).poly(dI-dC) is known to adopt an unusual B-form in low-salt aqueous solution, which is transformed into a standard B-form by the combination of perchlorate and ethanol. NiCl2 then transforms poly(dI-dC).poly(dI-dC) into the Z'-form, which is also adopted by poly(dI-br5dC).poly(dI-br5dC).

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Selected References

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  1. Behe M., Felsenfeld G. Effects of methylation on a synthetic polynucleotide: the B--Z transition in poly(dG-m5dC).poly(dG-m5dC). Proc Natl Acad Sci U S A. 1981 Mar;78(3):1619–1623. doi: 10.1073/pnas.78.3.1619. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Benevides J. M., Wang A. H., Rich A., Kyogoku Y., van der Marel G. A., van Boom J. H., Thomas G. J., Jr Raman spectra of single crystals of r(GCG)d(CGC) and d(CCCCGGGG) as models for A DNA, their structure transitions in aqueous solution, and comparison with double-helical poly(dG).poly(dC). Biochemistry. 1986 Jan 14;25(1):41–50. doi: 10.1021/bi00349a007. [DOI] [PubMed] [Google Scholar]
  3. Bernués J., Beltrán R., Casasnovas J. M., Azorín F. DNA-sequence and metal-ion specificity of the formation of *H-DNA. Nucleic Acids Res. 1990 Jul 25;18(14):4067–4073. doi: 10.1093/nar/18.14.4067. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bloomfield V. A. Condensation of DNA by multivalent cations: considerations on mechanism. Biopolymers. 1991 Nov;31(13):1471–1481. doi: 10.1002/bip.360311305. [DOI] [PubMed] [Google Scholar]
  5. Borah B., Cohen J. S., Howard F. B., Miles H. T. Poly(d2NH2A-dT): two-dimensional NMR shows a B to A conversion in high salt. Biochemistry. 1985 Dec 3;24(25):7456–7462. doi: 10.1021/bi00346a064. [DOI] [PubMed] [Google Scholar]
  6. Bourtayre P., Liquier J., Pizzorni L., Taillandier E. Z form of poly d(A-T).poly d(A-T) in solution studied by CD and UV spectroscopies. J Biomol Struct Dyn. 1987 Aug;5(1):97–104. doi: 10.1080/07391102.1987.10506378. [DOI] [PubMed] [Google Scholar]
  7. Breslow R., Guo T. Surface tension measurements show that chaotropic salting-in denaturants are not just water-structure breakers. Proc Natl Acad Sci U S A. 1990 Jan;87(1):167–169. doi: 10.1073/pnas.87.1.167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Chandrasekaran R., Puigjaner L. C., Arnott S., He R. G., Brahms S., Brahms J. The synthetic DNA duplex of poly d(Abr5U).poly d(Abr5U) adopts an A-DNA-like structure. J Biomol Struct Dyn. 1989 Feb;6(4):715–727. doi: 10.1080/07391102.1989.10507732. [DOI] [PubMed] [Google Scholar]
  9. DAVIES D. R., BALDWIN R. L. X-ray studies on two synthetic DNA copolymers. J Mol Biol. 1963 Apr;6:251–255. doi: 10.1016/s0022-2836(63)80086-8. [DOI] [PubMed] [Google Scholar]
  10. Deka R., Shriver M. D., Yu L. M., Jin L., Aston C. E., Chakraborty R., Ferrell R. E. Conservation of human chromosome 13 polymorphic microsatellite (CA)n repeats in chimpanzees. Genomics. 1994 Jul 1;22(1):226–230. doi: 10.1006/geno.1994.1369. [DOI] [PubMed] [Google Scholar]
  11. Drew H. R., Dickerson R. E. Conformation and dynamics in a Z-DNA tetramer. J Mol Biol. 1981 Nov 15;152(4):723–736. doi: 10.1016/0022-2836(81)90124-8. [DOI] [PubMed] [Google Scholar]
  12. Drew H. R., Dickerson R. E. Structure of a B-DNA dodecamer. III. Geometry of hydration. J Mol Biol. 1981 Sep 25;151(3):535–556. doi: 10.1016/0022-2836(81)90009-7. [DOI] [PubMed] [Google Scholar]
  13. Drew H., Takano T., Tanaka S., Itakura K., Dickerson R. E. High-salt d(CpGpCpG), a left-handed Z' DNA double helix. Nature. 1980 Aug 7;286(5773):567–573. doi: 10.1038/286567a0. [DOI] [PubMed] [Google Scholar]
  14. Gaillard C., Strauss F. Association of poly(CA).poly(TG) DNA fragments into four-stranded complexes bound by HMG1 and 2. Science. 1994 Apr 15;264(5157):433–436. doi: 10.1126/science.8153633. [DOI] [PubMed] [Google Scholar]
  15. Gray D. M., Ratliff R. L. Circular dichroism spectra of poly[d(AC):d(GT)], poly[r(AC):r(GU)], and hybrids poly[d(AC):r(GU)] and poly[r(AC):d(GT)] in the presence of ethanol. Biopolymers. 1975 Mar;14(3):487–498. doi: 10.1002/bip.1975.360140305. [DOI] [PubMed] [Google Scholar]
  16. Hall K. B., Maestre M. F. Temperature-dependent reversible transition of poly(dCdG).poly(dCdG) in ethanolic and methanolic solutions. Biopolymers. 1984 Nov;23(11 Pt 1):2127–2139. doi: 10.1002/bip.360231103. [DOI] [PubMed] [Google Scholar]
  17. Harder M. E., Johnson W. C., Jr Stabilization of the Z' form of poly(dGdC):poly(dGdC) in solution by multivalent ions relates to the ZII form in crystals. Nucleic Acids Res. 1990 Apr 25;18(8):2141–2148. doi: 10.1093/nar/18.8.2141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Hartmann B., Pilet J., Ptak M., Ramstein J., Malfoy B., Leng M. The B reversible Z transition of poly(dI-br5dC).poly(dI-br5dC). A quantitative description of the Z form dynamic structure. Nucleic Acids Res. 1982 May 25;10(10):3261–3277. doi: 10.1093/nar/10.10.3261. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Ivanov V. I., Minchenkova L. E., Minyat E. E., Frank-Kamenetskii M. D., Schyolkina A. K. The B to A transition of DNA in solution. J Mol Biol. 1974 Aug 25;87(4):817–833. doi: 10.1016/0022-2836(74)90086-2. [DOI] [PubMed] [Google Scholar]
  20. Jovin T. M., McIntosh L. P., Arndt-Jovin D. J., Zarling D. A., Robert-Nicoud M., van de Sande J. H., Jorgenson K. F., Eckstein F. Left-handed DNA: from synthetic polymers to chromosomes. J Biomol Struct Dyn. 1983 Oct;1(1):21–57. doi: 10.1080/07391102.1983.10507425. [DOI] [PubMed] [Google Scholar]
  21. Kirnos M. D., Khudyakov I. Y., Alexandrushkina N. I., Vanyushin B. F. 2-aminoadenine is an adenine substituting for a base in S-2L cyanophage DNA. Nature. 1977 Nov 24;270(5635):369–370. doi: 10.1038/270369a0. [DOI] [PubMed] [Google Scholar]
  22. Kypr J., Penázová H., Sági J., Pospísilová S., Vorlícková M. UV light-induced crosslinking of the strands of poly(dA-dT) and related alternating purine-pyrimidine DNAs. J Biomol Struct Dyn. 1994 Jun;11(6):1225–1236. doi: 10.1080/07391102.1994.10508065. [DOI] [PubMed] [Google Scholar]
  23. Kypr J., Sági J., Szakonyi E., Ebinger K., Penázová H., Chládková J., Vorlícková M. Thymine methyl groups stabilize the putative A-form of the synthetic DNA poly(amino2dA-dT). Biochemistry. 1994 Apr 5;33(13):3801–3806. doi: 10.1021/bi00179a003. [DOI] [PubMed] [Google Scholar]
  24. Leslie A. G., Arnott S., Chandrasekaran R., Ratliff R. L. Polymorphism of DNA double helices. J Mol Biol. 1980 Oct 15;143(1):49–72. doi: 10.1016/0022-2836(80)90124-2. [DOI] [PubMed] [Google Scholar]
  25. Mirau P. A., Kearns D. R., McIntosh L. P., Jovin T. M. 1H nuclear magnetic resonance study of the dynamic properties of the B and Z-forms of poly[d(A-br5C).d(G-T)]. J Mol Biol. 1986 Dec 5;192(3):633–643. doi: 10.1016/0022-2836(86)90281-0. [DOI] [PubMed] [Google Scholar]
  26. Miskovsky P., Tomkova A., Chinsky L., Turpin P. Y. Conformational transitions of poly(dI-dC) in aqueous solution as studied by ultraviolet resonance Raman spectroscopy. J Biomol Struct Dyn. 1993 Dec;11(3):655–669. doi: 10.1080/07391102.1993.10508021. [DOI] [PubMed] [Google Scholar]
  27. Mitsui Y., Langridge R., Shortle B. E., Cantor C. R., Grant R. C., Kodama M., Wells R. D. Physical and enzymatic studies on poly d(I-C)-poly d(I-C), an unusual double-helical DNA. Nature. 1970 Dec 19;228(5277):1166–1169. doi: 10.1038/2281166a0. [DOI] [PubMed] [Google Scholar]
  28. Nishimura Y., Torigoe C., Tsuboi M. Salt induced B----A transition of poly(dG).poly(dC) and the stabilization of A form by its methylation. Nucleic Acids Res. 1986 Mar 25;14(6):2737–2748. doi: 10.1093/nar/14.6.2737. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Patel D. J., Canuel L. L., Pohl F. M. "Alternating B-DNA" conformation for the oligo(dG-dC) duplex in high-salt solution. Proc Natl Acad Sci U S A. 1979 Jun;76(6):2508–2511. doi: 10.1073/pnas.76.6.2508. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Patel U., Grundfest-Broniatowski S., Gupta M., Banerjee S. Microsatellite instabilities at five chromosomes in primary breast tumors. Oncogene. 1994 Dec;9(12):3695–3700. [PubMed] [Google Scholar]
  31. Pohl F. M., Jovin T. M. Salt-induced co-operative conformational change of a synthetic DNA: equilibrium and kinetic studies with poly (dG-dC). J Mol Biol. 1972 Jun 28;67(3):375–396. doi: 10.1016/0022-2836(72)90457-3. [DOI] [PubMed] [Google Scholar]
  32. Pohl F. M. Polymorphism of a synthetic DNA in solution. Nature. 1976 Mar 25;260(5549):365–366. doi: 10.1038/260365a0. [DOI] [PubMed] [Google Scholar]
  33. Rao M. V., Atreyi M., Kumar G. S., Kumar S. Reversal of the long-wavelength CD band of poly(dI-dC).poly(dI-dC) on specific interaction with the 53-58 peptide fragment of the lac repressor. Biopolymers. 1987 Mar;26(3):329–332. doi: 10.1002/bip.360260302. [DOI] [PubMed] [Google Scholar]
  34. Rhyu M. G., Park W. S., Meltzer S. J. Microsatellite instability occurs frequently in human gastric carcinoma. Oncogene. 1994 Jan;9(1):29–32. [PubMed] [Google Scholar]
  35. Riazance-Lawrence J. H., Johnson W. C., Jr Multivalent ions are necessary for poly[d(AC).d(GT)] to assume the Z form: a CD study. Biopolymers. 1992 Mar;32(3):271–276. doi: 10.1002/bip.360320307. [DOI] [PubMed] [Google Scholar]
  36. Riazance J. H., Johnson W. C., Jr, McIntosh L. P., Jovin T. M. Vacuum UV circular dichroism is diagnostic for the left-handed Z form of poly [d(A-C).d(G-T)] and other polydeoxynucleotides. Nucleic Acids Res. 1987 Sep 25;15(18):7627–7636. doi: 10.1093/nar/15.18.7627. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Sarkar G., Paynton C., Sommer S. S. Segments containing alternating purine and pyrimidine dinucleotides: patterns of polymorphism in humans and prevalence throughout phylogeny. Nucleic Acids Res. 1991 Feb 11;19(3):631–636. doi: 10.1093/nar/19.3.631. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Sarma M. H., Gupta G., Sarma R. H. 500-MHz 1H NMR study of poly(dG).poly(dC) in solution using one-dimensional nuclear Overhauser effect. Biochemistry. 1986 Jun 17;25(12):3659–3665. doi: 10.1021/bi00360a028. [DOI] [PubMed] [Google Scholar]
  39. Shin Y. A., Feroli S. L., Eichhorn G. L. Psi compaction of poly[d(AT)].poly[d(AT)]. Biopolymers. 1986 Nov;25(11):2133–2148. doi: 10.1002/bip.360251108. [DOI] [PubMed] [Google Scholar]
  40. Soumpasis D. M., Wiechen J., Jovin T. M. Relative stabilities and transitions of DNA conformations in 1:1 electrolytes: a theoretical study. J Biomol Struct Dyn. 1987 Feb;4(4):535–552. doi: 10.1080/07391102.1987.10507658. [DOI] [PubMed] [Google Scholar]
  41. Sági J., Otvös L. Modified polynucleotides. V. Slow-down of nuclease action by 5-alkyluracil-containing DNAs. Biochem Biophys Res Commun. 1980 Jul 16;95(1):156–162. doi: 10.1016/0006-291x(80)90717-2. [DOI] [PubMed] [Google Scholar]
  42. Sági J., Szemzö A., Otvös L., Vorlícková M., Kypr J. Destabilization of the duplex and the high-salt Z-form of poly(dG-methyl5dC) by substitution of ethyl for the 5-methyl group. Int J Biol Macromol. 1991 Dec;13(6):329–336. doi: 10.1016/0141-8130(91)90013-k. [DOI] [PubMed] [Google Scholar]
  43. Thomas T. J., Bloomfield V. A. Quasielastic laser light scattering and electron microscopy studies of the conformational transitions and condensation of poly(dA-dT).poly(dA-dT). Biopolymers. 1985 Dec;24(12):2185–2194. doi: 10.1002/bip.360241203. [DOI] [PubMed] [Google Scholar]
  44. Uchida T., Wada C., Wang C., Ishida H., Egawa S., Yokoyama E., Ohtani H., Koshiba K. Microsatellite instability in prostate cancer. Oncogene. 1995 Mar 2;10(5):1019–1022. [PubMed] [Google Scholar]
  45. Vogt P. Potential genetic functions of tandem repeated DNA sequence blocks in the human genome are based on a highly conserved "chromatin folding code". Hum Genet. 1990 Mar;84(4):301–336. doi: 10.1007/BF00196228. [DOI] [PubMed] [Google Scholar]
  46. Vorlickova M., Sagi J., Szabolcs A., Szemzo A., Otvos L., Kypr J. Poly(amino2dA-dT) isomerizes into the unusual X-DNA double helix at physiological conditions inducing Z-DNA in poly (dG-methyl5dC). J Biomol Struct Dyn. 1988 Dec;6(3):503–510. doi: 10.1080/07391102.1988.10506503. [DOI] [PubMed] [Google Scholar]
  47. Vorlicková M., Khudyakov IYa, Hejtmánková I., Kypr J. Circular dichroism studies of salt- and alcohol- induced conformational changes in cyanophage S-2L DNA which contains amino 2 adenine instead of adenine. J Biomol Struct Dyn. 1991 Aug;9(1):81–85. doi: 10.1080/07391102.1991.10507894. [DOI] [PubMed] [Google Scholar]
  48. Vorlicková M., Sági J., Hejtmánková I., Kypr J. Alkyl substituent in place of the thymine methyl group controls the A-X conformational bimorphism in poly(dA-dT). J Biomol Struct Dyn. 1991 Dec;9(3):571–578. doi: 10.1080/07391102.1991.10507937. [DOI] [PubMed] [Google Scholar]
  49. Vorlícková M., Chládková J., Kypr J. Conformational transitions of poly(dA-bromo5dU) and poly(dA-iodo5dU) in solution. Nucleic Acids Res. 1992 Mar 11;20(5):1109–1112. doi: 10.1093/nar/20.5.1109. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Vorlícková M., Kypr J. Conformational variability of poly(dA-dT).poly(dA-dT) and some other deoxyribonucleic acids includes a novel type of double helix. J Biomol Struct Dyn. 1985 Aug;3(1):67–83. doi: 10.1080/07391102.1985.10508399. [DOI] [PubMed] [Google Scholar]
  51. Vorlícková M., Kypr J., Sklenár V. Salt-induced conformational transition of poly[d(A-T)] X poly[d(A-T)]. J Mol Biol. 1983 May 5;166(1):85–92. doi: 10.1016/s0022-2836(83)80052-7. [DOI] [PubMed] [Google Scholar]
  52. Vorlícková M., Sedlácek P., Kypr J., Sponar J. Conformational transitions of poly(dA-dT)poly(dA-dT) in ethanolic solutions. Nucleic Acids Res. 1982 Nov 11;10(21):6969–6979. doi: 10.1093/nar/10.21.6969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Vorlícková M., Sági J. Transitions of poly(dI-dC), poly(dI-methyl5dC) and poly(dI-bromo5dC) among and within the B-, Z-, A- and X-DNA families of conformations. Nucleic Acids Res. 1991 May 11;19(9):2343–2347. doi: 10.1093/nar/19.9.2343. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Wang A. J., Quigley G. J., Kolpak F. J., van der Marel G., van Boom J. H., Rich A. Left-handed double helical DNA: variations in the backbone conformation. Science. 1981 Jan 9;211(4478):171–176. doi: 10.1126/science.7444458. [DOI] [PubMed] [Google Scholar]
  55. Wells R. D., Larson J. E., Grant R. C., Shortle B. E., Cantor C. R. Physicochemical studies on polydeoxyribonucleotides containing defined repeating nucleotide sequences. J Mol Biol. 1970 Dec 28;54(3):465–497. doi: 10.1016/0022-2836(70)90121-x. [DOI] [PubMed] [Google Scholar]
  56. Winterø A. K., Fredholm M., Thomsen P. D. Variable (dG-dT)n.(dC-dA)n sequences in the porcine genome. Genomics. 1992 Feb;12(2):281–288. doi: 10.1016/0888-7543(92)90375-3. [DOI] [PubMed] [Google Scholar]
  57. Xu Q., Jampani S. R., Braunlin W. H. Rotational dynamics of hexaamminecobalt(III) bound to oligomeric DNA: correlation with cation-induced structural transitions. Biochemistry. 1993 Nov 9;32(44):11754–11760. doi: 10.1021/bi00095a002. [DOI] [PubMed] [Google Scholar]
  58. Xu Q., Shoemaker R. K., Braunlin W. H. Induction of B-A transitions of deoxyoligonucleotides by multivalent cations in dilute aqueous solution. Biophys J. 1993 Sep;65(3):1039–1049. doi: 10.1016/S0006-3495(93)81163-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Zehfus M. H., Johnson W. C., Jr Conformation of P-form DNA. Biopolymers. 1984 Jul;23(7):1269–1281. doi: 10.1002/bip.360230711. [DOI] [PubMed] [Google Scholar]
  60. Zehfus M. H., Johnson W. C., Jr Properties of P-form DNA as revealed by circular dichroism. Biopolymers. 1981 Aug;20(8):1589–1603. doi: 10.1002/bip.1981.360200803. [DOI] [PubMed] [Google Scholar]
  61. Zenklusen J. C., Bièche I., Lidereau R., Conti C. J. (C-A)n microsatellite repeat D7S522 is the most commonly deleted region in human primary breast cancer. Proc Natl Acad Sci U S A. 1994 Dec 6;91(25):12155–12158. doi: 10.1073/pnas.91.25.12155. [DOI] [PMC free article] [PubMed] [Google Scholar]

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