Abstract
Extensive circular dichroism studies have been conducted with the title polynucleotides under various solution conditions. The studies provided the following information: (i) The halogen atoms in place of thymine methyl hinder the isomerization into X-DNA. (ii) The brominated but not iodinated polynucleotide isomerizes into Z-DNA in concentrated NaCl+NiCl2. The transition takes place at lower NiCl2 concentrations than with poly(dA-dT). (iii) The iodinated polynucleotide forms an unusual conformation in aqueous solution in which it is very stable. It isomerizes from this conformer into the usual B-type double helix in concentrated ethanol solutions. The isomerization is a two-state cooperative process. (iv) Both title polynucleotides undergo still another two-state cooperative transition in trifluorethanol solutions presumably into A-DNA showing a rather unusual circular dichroism spectrum.
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Selected References
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- Adam S., Liquier J., Taboury J. A., Taillandier E. Right- and left-handed helixes of poly[d(A-T)].poly[d(A-T)] investigated by infrared spectroscopy. Biochemistry. 1986 Jun 3;25(11):3220–3225. doi: 10.1021/bi00359a021. [DOI] [PubMed] [Google Scholar]
- BALDWIN R. L., SHOOTER E. M. THE ALKALINE TRANSITION OF BU-CONTAINING DNA AND ITS BEARING ON THE REPLICATION OF DNA. J Mol Biol. 1963 Nov;7:511–526. doi: 10.1016/s0022-2836(63)80098-4. [DOI] [PubMed] [Google Scholar]
- 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]
- Cohen J. S., Wooten J. B., Chatterjee C. L. Characterization of alternating deoxyribonucleic acid conformations in solution by phosphorus-31 nuclear magnetic resonance spectroscopy. Biochemistry. 1981 May 26;20(11):3049–3055. doi: 10.1021/bi00514a010. [DOI] [PubMed] [Google Scholar]
- Corin A. F., Jovin T. M. Proflavin binding to poly[d(A-T)] and poly[d(A-br5U)]: triplet state and temperature-jump kinetics. Biochemistry. 1986 Jul 15;25(14):3995–4007. doi: 10.1021/bi00362a004. [DOI] [PubMed] [Google Scholar]
- Driggers P. H., Beattie K. L. Effect of pH on the base-mispairing properties of 5-bromouracil during DNA synthesis. Biochemistry. 1988 Mar 8;27(5):1729–1735. doi: 10.1021/bi00405a052. [DOI] [PubMed] [Google Scholar]
- Fazakerley G. V., Sowers L. C., Eritja R., Kaplan B. E., Goodman M. F. Structural and dynamic properties of a bromouracil-adenine base pair in DNA studied by proton NMR. J Biomol Struct Dyn. 1987 Dec;5(3):639–650. doi: 10.1080/07391102.1987.10506417. [DOI] [PubMed] [Google Scholar]
- INMAN R. B., BALDWIN R. L. Formation of hybrid molecules from two alternating DNA copolymers. J Mol Biol. 1962 Aug;5:185–200. doi: 10.1016/s0022-2836(62)80083-7. [DOI] [PubMed] [Google Scholar]
- INMAN R. B., BALDWIN R. L. Helix-random coil transitions in synthetic DNAs of alternating sequence. J Mol Biol. 1962 Aug;5:172–184. doi: 10.1016/s0022-2836(62)80082-5. [DOI] [PubMed] [Google Scholar]
- Ivanov V. I., Krylov DYu, Minyat E. E. Three-state diagram for DNA. J Biomol Struct Dyn. 1985 Aug;3(1):43–55. doi: 10.1080/07391102.1985.10508397. [DOI] [PubMed] [Google Scholar]
- 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]
- Klug A., Jack A., Viswamitra M. A., Kennard O., Shakked Z., Steitz T. A. A hypothesis on a specific sequence-dependent conformation of DNA and its relation to the binding of the lac-repressor protein. J Mol Biol. 1979 Jul 15;131(4):669–680. doi: 10.1016/0022-2836(79)90196-7. [DOI] [PubMed] [Google Scholar]
- Kypr J., Sági J., Szabolcs A., Ebinger K., Otvös L., Vorlícková M. Two distinct conformers coexist in a synthetic DNA poly(dA-dT).Poly(dA-dT) in low-salt aqueous solution. Gen Physiol Biophys. 1990 Aug;9(4):415–418. [PubMed] [Google Scholar]
- Kypr J., Vorlícková M. Conformations of alternating purine-pyrimidine DNAs in high-CsF solutions and their reversal by dipyrandium, ethidium and high temperature. Biochim Biophys Acta. 1985 Feb 15;838(2):244–251. doi: 10.1016/0304-4165(85)90085-6. [DOI] [PubMed] [Google Scholar]
- Kypr J., Vorlícková M. RNA-like conformational properties of a synthetic DNA poly(dA-dU).poly(dA-dU). Biochem Biophys Res Commun. 1985 Oct 15;132(1):95–99. doi: 10.1016/0006-291x(85)90993-3. [DOI] [PubMed] [Google Scholar]
- Lin S. Y., Riggs A. D. Lac repressor binding to operator analogues: comparison of poly(d(A-T)), poly(d(A-BrU)), and poly(d(A-U)). Biochem Biophys Res Commun. 1971 Dec 17;45(6):1542–1547. doi: 10.1016/0006-291x(71)90195-1. [DOI] [PubMed] [Google Scholar]
- Lin S. Y., Riggs A. D. The binding of lac repressor and the catabolite gene activator protein to halogen-substituted analogues of poly[d(A-T)]. Biochim Biophys Acta. 1976 May 3;432(2):185–191. doi: 10.1016/0005-2787(76)90160-x. [DOI] [PubMed] [Google Scholar]
- Malfoy B., Rousseau N., Leng M. Interaction between antibodies to Z-form deoxyribonucleic acid and double-stranded polynucleotides. Biochemistry. 1982 Oct 26;21(22):5463–5467. doi: 10.1021/bi00265a013. [DOI] [PubMed] [Google Scholar]
- 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]
- Petruska J., Horn D. Sequence-specific responses of restriction endonucleases to bromodeoxyuridine substitution in mammalian DNA. Nucleic Acids Res. 1983 Apr 25;11(8):2495–2510. doi: 10.1093/nar/11.8.2495. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Privé G. G., Yanagi K., Dickerson R. E. Structure of the B-DNA decamer C-C-A-A-C-G-T-T-G-G and comparison with isomorphous decamers C-C-A-A-G-A-T-T-G-G and C-C-A-G-G-C-C-T-G-G. J Mol Biol. 1991 Jan 5;217(1):177–199. doi: 10.1016/0022-2836(91)90619-h. [DOI] [PubMed] [Google Scholar]
- Sponer J., Kypr J. Base pair buckling can eliminate the interstrand purine clash at the CpG steps in B-DNA caused by the base pair propeller twisting. J Biomol Struct Dyn. 1990 Jun;7(6):1211–1220. doi: 10.1080/07391102.1990.10508560. [DOI] [PubMed] [Google Scholar]
- 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]
- Viswamitra M. A., Kennard O., Jones P. G., Sheldrick G. M., Salisbury S., Favello L., Shakked Z. DNA double helical fragment at atomic resolution. Nature. 1978 Jun 22;273(5664):687–688. doi: 10.1038/273687a0. [DOI] [PubMed] [Google Scholar]
- 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]
- Vorlícková M., Kypr J., Jovin T. M., Planck M. CD of the synthetic RNA duplexes poly[r(A-T)] and poly[r(A-U)] in salt and ethanolic solutions. Biopolymers. 1990 Feb 5;29(2):385–392. doi: 10.1002/bip.360290210. [DOI] [PubMed] [Google Scholar]
- 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]
- 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]
- 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]
- WAKE R. G., BALDWIN R. L. Physical studies on the replication of DNA in vitro. J Mol Biol. 1962 Aug;5:201–216. doi: 10.1016/s0022-2836(62)80084-9. [DOI] [PubMed] [Google Scholar]
- Wick K. L., Matthews K. S. Interactions between lac repressor protein and site-specific bromodeoxyuridine-substituted operator DNA. Ultraviolet footprinting and protein-DNA cross-link formation. J Biol Chem. 1991 Apr 5;266(10):6106–6112. [PubMed] [Google Scholar]
- Wright W. E. BUdR, probability and cell variants: towards a molecular understanding of the decision to differentiate. Bioessays. 1985 Dec;3(6):245–248. doi: 10.1002/bies.950030603. [DOI] [PubMed] [Google Scholar]
