Abstract
Differential scanning microcalorimetry (DSC), UV absorption and circular dichroism (CD) have been used to study structure and stability of linear (lin), open circular (oc), supercoiled (cd) and relaxed circular duplex (rd) DNA and calf thymus (CT) DNA. Investigations were made in low salt buffer and in the presence of 7.2 M NaClO4. The chaotropic action of perchlorate promotes a reduction of the overall stability of DNA, which permits a direct determination of the transition enthalpies of all four DNA configurations. The stabilities against thermal denaturation have been found to increase in the series lin approximately oc less than cd less than rd. These relative stabilities can be rationalized on the basis of the linkage between supercoiling and secondary structural changes in topologically constrained duplex DNA. On the basis of these studies, a model of the melting process could be suggested that is consistent with the energetic and spectroscopic data.
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Selected References
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- Anderson P., Bauer W. Supercoiling in closed circular DNA: dependence upon ion type and concentration. Biochemistry. 1978 Feb 21;17(4):594–601. doi: 10.1021/bi00597a006. [DOI] [PubMed] [Google Scholar]
- Atkinson A., Gatenby A. D., Lowe A. G. The determination of inorganic orthophosphate in biological systems. Biochim Biophys Acta. 1973 Aug 17;320(1):195–204. doi: 10.1016/0304-4165(73)90178-5. [DOI] [PubMed] [Google Scholar]
- Baase W. A., Johnson W. C., Jr Circular dichroism and DNA secondary structure. Nucleic Acids Res. 1979 Feb;6(2):797–814. doi: 10.1093/nar/6.2.797. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bauer W. R. Structure and reactions of closed duplex DNA. Annu Rev Biophys Bioeng. 1978;7:287–313. doi: 10.1146/annurev.bb.07.060178.001443. [DOI] [PubMed] [Google Scholar]
- Bauer W. R. Structure of DNA in denaturing solvents. I. Bacteriophage PM2 DNA in aqueous sodium perchlorate. J Mol Biol. 1972 Jun 20;67(2):183–198. doi: 10.1016/0022-2836(72)90235-5. [DOI] [PubMed] [Google Scholar]
- Beard P., Morrow J. F., Berg P. Cleavage of circular, superhelical simian virus 40 DNA to a linear duplex by S1 nuclease. J Virol. 1973 Dec;12(6):1303–1313. doi: 10.1128/jvi.12.6.1303-1313.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bernstein L. B., Mount S. M., Weiner A. M. Pseudogenes for human small nuclear RNA U3 appear to arise by integration of self-primed reverse transcripts of the RNA into new chromosomal sites. Cell. 1983 Feb;32(2):461–472. doi: 10.1016/0092-8674(83)90466-x. [DOI] [PubMed] [Google Scholar]
- Borovik A. S., Kalambet Y. A., Lyubchenko Y. L., Shitov V. T., Golovanov E. I. Equilibrium melting of plasmid ColE1 DNA: electron-microscopic visualization. Nucleic Acids Res. 1980 Sep 25;8(18):4165–4184. doi: 10.1093/nar/8.18.4165. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brahms S., Brahms J., Van Holde K. E. Nature of conformational changes in poly[d(A-T)-d(A-T)] in the premelting region. Proc Natl Acad Sci U S A. 1976 Oct;73(10):3453–3457. doi: 10.1073/pnas.73.10.3453. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Burke R. L., Bauer W. R. The early melting of closed duplex DNA: analysis by banding in buoyant neutral rubidium trichloroacetate. Nucleic Acids Res. 1980 Mar 11;8(5):1145–1165. doi: 10.1093/nar/8.5.1145. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Burke R. L., Bauer W. R. The helix-coil transition of closed and nicked DNAs in aqueous neutral trichloroacetate solutions. Nucleic Acids Res. 1978 Dec;5(12):4819–4836. doi: 10.1093/nar/5.12.4819. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chan A., Kilkuskie R., Hanlon S. Correlations between the duplex winding angle and the circular dichroism spectrum of calf thymus DNA. Biochemistry. 1979 Jan 9;18(1):84–91. doi: 10.1021/bi00568a013. [DOI] [PubMed] [Google Scholar]
- Crick F. H. Linking numbers and nucleosomes. Proc Natl Acad Sci U S A. 1976 Aug;73(8):2639–2643. doi: 10.1073/pnas.73.8.2639. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Depew D. E., Wang J. C. Conformational fluctuations of DNA helix. Proc Natl Acad Sci U S A. 1975 Nov;72(11):4275–4279. doi: 10.1073/pnas.72.11.4275. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Drew H. R., Wing R. M., Takano T., Broka C., Tanaka S., Itakura K., Dickerson R. E. Structure of a B-DNA dodecamer: conformation and dynamics. Proc Natl Acad Sci U S A. 1981 Apr;78(4):2179–2183. doi: 10.1073/pnas.78.4.2179. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Finch J. T., Lutter L. C., Rhodes D., Brown R. S., Rushton B., Levitt M., Klug A. Structure of nucleosome core particles of chromatin. Nature. 1977 Sep 1;269(5623):29–36. doi: 10.1038/269029a0. [DOI] [PubMed] [Google Scholar]
- Furlong J. C., Lilley D. M. Highly selective chemical modification of cruciform loops by diethyl pyrocarbonate. Nucleic Acids Res. 1986 May 27;14(10):3995–4007. doi: 10.1093/nar/14.10.3995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gagua A. V., Belintsev B. N., Lyubchenko YuL Effect of base-pair stability on the melting of superhelical DNA. Nature. 1981 Dec 17;294(5842):662–663. doi: 10.1038/294662a0. [DOI] [PubMed] [Google Scholar]
- Gellert M., Mizuuchi K., O'Dea M. H., Nash H. A. DNA gyrase: an enzyme that introduces superhelical turns into DNA. Proc Natl Acad Sci U S A. 1976 Nov;73(11):3872–3876. doi: 10.1073/pnas.73.11.3872. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gennis R. B., Cantor C. R. Optical studies of a conformational change in DNA before melting. J Mol Biol. 1972 Apr 14;65(3):381–399. doi: 10.1016/0022-2836(72)90196-9. [DOI] [PubMed] [Google Scholar]
- Gray D. M., Taylor T. N., Lang D. Dehydrated circular DNA: circular dichroism of molecules in ethanolic solutions. Biopolymers. 1978 Jan;17(1):145–157. doi: 10.1002/bip.1978.360170111. [DOI] [PubMed] [Google Scholar]
- Greve J., Maestre M. F., Levin A. Circular dichroism of adenine and thymine containing synthetic polynucleotides. Biopolymers. 1977 Jul;16(7):1489–1504. doi: 10.1002/bip.1977.360160709. [DOI] [PubMed] [Google Scholar]
- Haniford D. B., Pulleyblank D. E. Facile transition of poly[d(TG) x d(CA)] into a left-handed helix in physiological conditions. Nature. 1983 Apr 14;302(5909):632–634. doi: 10.1038/302632a0. [DOI] [PubMed] [Google Scholar]
- Hanlon S., Chan A., Berman S. Specific cation effects on conformational transitions of DNA in aqueous solutions. Biochim Biophys Acta. 1978 Jul 24;519(2):526–536. doi: 10.1016/0005-2787(78)90105-3. [DOI] [PubMed] [Google Scholar]
- Hays J. B., Boehmer S. Antagonists of DNA gyrase inhibit repair and recombination of UV-irradiated phage lambda. Proc Natl Acad Sci U S A. 1978 Sep;75(9):4125–4129. doi: 10.1073/pnas.75.9.4125. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Helland D., Nes I. F., Kleppe K. Mammalian DNA-repair endonuclease acts only on supercoiled DNA. FEBS Lett. 1982 Jun 1;142(1):121–124. doi: 10.1016/0014-5793(82)80233-0. [DOI] [PubMed] [Google Scholar]
- Ivanov V. I., Minchenkova L. E., Schyolkina A. K., Poletayev A. I. Different conformations of double-stranded nucleic acid in solution as revealed by circular dichroism. Biopolymers. 1973;12(1):89–110. doi: 10.1002/bip.1973.360120109. [DOI] [PubMed] [Google Scholar]
- Johnson B. B., Dahl K. S., Tinoco I., Jr, Ivanov V. I., Zhurkin V. B. Correlations between deoxyribonucleic acid structural parameters and calculated circular dichroism spectra. Biochemistry. 1981 Jan 6;20(1):73–78. doi: 10.1021/bi00504a013. [DOI] [PubMed] [Google Scholar]
- Kikuchi A., Asai K. Reverse gyrase--a topoisomerase which introduces positive superhelical turns into DNA. Nature. 1984 Jun 21;309(5970):677–681. doi: 10.1038/309677a0. [DOI] [PubMed] [Google Scholar]
- Klump H., Burkart W. Calorimetric measurements of the transition enthalpy of DNA in aqueous urea solutions. Biochim Biophys Acta. 1977 Apr 19;475(4):601–604. doi: 10.1016/0005-2787(77)90320-3. [DOI] [PubMed] [Google Scholar]
- Krasnow M. A., Cozzarelli N. R. Site-specific relaxation and recombination by the Tn3 resolvase: recognition of the DNA path between oriented res sites. Cell. 1983 Apr;32(4):1313–1324. doi: 10.1016/0092-8674(83)90312-4. [DOI] [PubMed] [Google Scholar]
- Kłysik J., Stirdivant S. M., Larson J. E., Hart P. A., Wells R. D. Left-handed DNA in restriction fragments and a recombinant plasmid. Nature. 1981 Apr 23;290(5808):672–677. doi: 10.1038/290672a0. [DOI] [PubMed] [Google Scholar]
- Laiken N. Theoretical model for the equilibrium behavior of DNA superhelices. Biopolymers. 1973;12(1):11–26. doi: 10.1002/bip.1973.360120103. [DOI] [PubMed] [Google Scholar]
- Lilley D. M. The inverted repeat as a recognizable structural feature in supercoiled DNA molecules. Proc Natl Acad Sci U S A. 1980 Nov;77(11):6468–6472. doi: 10.1073/pnas.77.11.6468. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lilley D. M. The kinetic properties of cruciform extrusion are determined by DNA base-sequence. Nucleic Acids Res. 1985 Mar 11;13(5):1443–1465. doi: 10.1093/nar/13.5.1443. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Litman R. M. A deoxyribonucleic acid polymerase from Micrococcus luteus (Micrococcus lysodeikticus) isolated on deoxyribonucleic acid-cellulose. J Biol Chem. 1968 Dec 10;243(23):6222–6233. [PubMed] [Google Scholar]
- Liu L. F., Liu C. C., Alberts B. M. T4 DNA topoisomerase: a new ATP-dependent enzyme essential for initiation of T4 bacteriophage DNA replication. Nature. 1979 Oct 11;281(5731):456–461. doi: 10.1038/281456a0. [DOI] [PubMed] [Google Scholar]
- Maeda Y., Ohtsubo E. Relationship between helix-coil transition and gene organization of ColE1 plasmid DNA. Differential scanning calorimetric and theoretical studies. J Mol Biol. 1987 Apr 20;194(4):691–698. doi: 10.1016/0022-2836(87)90246-4. [DOI] [PubMed] [Google Scholar]
- Maestre M. F., Wang J. C. Circular dichroism of superhelical DNA. Biopolymers. 1971 Jun;10(6):1021–1030. doi: 10.1002/bip.360100608. [DOI] [PubMed] [Google Scholar]
- Mizuuchi K., Gellert M., Nash H. A. Involement of supertwisted DNA in integrative recombination of bacteriophage lambda. J Mol Biol. 1978 May 25;121(3):375–392. doi: 10.1016/0022-2836(78)90370-4. [DOI] [PubMed] [Google Scholar]
- Mizuuchi K., Mizuuchi M., Gellert M. Cruciform structures in palindromic DNA are favored by DNA supercoiling. J Mol Biol. 1982 Apr 5;156(2):229–243. doi: 10.1016/0022-2836(82)90325-4. [DOI] [PubMed] [Google Scholar]
- Palecek E. Premelting changes in DNA conformation. Prog Nucleic Acid Res Mol Biol. 1976;18:151–213. [PubMed] [Google Scholar]
- Peck L. J., Nordheim A., Rich A., Wang J. C. Flipping of cloned d(pCpG)n.d(pCpG)n DNA sequences from right- to left-handed helical structure by salt, Co(III), or negative supercoiling. Proc Natl Acad Sci U S A. 1982 Aug;79(15):4560–4564. doi: 10.1073/pnas.79.15.4560. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Perahia D., Jhon M. S., Pullman B. Theoretical study of the hydration of B-DNA. Biochim Biophys Acta. 1977 Feb 3;474(3):349–362. doi: 10.1016/0005-2787(77)90265-9. [DOI] [PubMed] [Google Scholar]
- Platt J. R. POSSIBLE SEPARATION OF INTERTWINED NUCLEIC ACID CHAINS BY TRANSFER-TWIST. Proc Natl Acad Sci U S A. 1955 Mar 15;41(3):181–183. doi: 10.1073/pnas.41.3.181. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Richardson J. P. Effects of supercoiling on transcription from bacteriophage PM2 deoxyribonucleic acid. Biochemistry. 1974 Jul 16;13(15):3164–3169. doi: 10.1021/bi00712a025. [DOI] [PubMed] [Google Scholar]
- Seidl A., Hinz H. J. The free energy of DNA supercoiling is enthalpy-determined. Proc Natl Acad Sci U S A. 1984 Mar;81(5):1312–1316. doi: 10.1073/pnas.81.5.1312. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shishido K. Relationship between S1 endonuclease-sensitivity and number of superhelical turns in a negatively-twisted DNA. FEBS Lett. 1980 Mar 10;111(2):333–336. doi: 10.1016/0014-5793(80)80821-0. [DOI] [PubMed] [Google Scholar]
- Sinden R. R., Pettijohn D. E. Cruciform transitions in DNA. J Biol Chem. 1984 May 25;259(10):6593–6600. [PubMed] [Google Scholar]
- Singleton C. K., Wells R. D. Relationship between superhelical density and cruciform formation in plasmid pVH51. J Biol Chem. 1982 Jun 10;257(11):6292–6295. [PubMed] [Google Scholar]
- Sprecher C. A., Johnson W. C., Jr Change in conformation of various DNAs on melting as followed by circular dichroism. Biopolymers. 1982 Feb;21(2):321–329. doi: 10.1002/bip.360210207. [DOI] [PubMed] [Google Scholar]
- Sternglanz R., DiNardo S., Voelkel K. A., Nishimura Y., Hirota Y., Becherer K., Zumstein L., Wang J. C. Mutations in the gene coding for Escherichia coli DNA topoisomerase I affect transcription and transposition. Proc Natl Acad Sci U S A. 1981 May;78(5):2747–2751. doi: 10.1073/pnas.78.5.2747. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Studdert D. S., Patroni M., Davis R. C. Circular dichroism of DNA: temperature and salt dependence. Biopolymers. 1972;11(4):761–779. doi: 10.1002/bip.1972.360110404. [DOI] [PubMed] [Google Scholar]
- Vinograd J., Lebowitz J. Physical and topological properties of circular DNA. J Gen Physiol. 1966 Jul;49(6):103–125. doi: 10.1085/jgp.49.6.103. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Voordouw G., Kam Z., Borochov N., Eisenberg H. Isolation and physical studies of the intact supercoiled, the open circular and the linear forms of ColE1-plasmid DNA. Biophys Chem. 1978 May;8(2):171–189. doi: 10.1016/0301-4622(78)80008-8. [DOI] [PubMed] [Google Scholar]
- Wada A., Yabuki S., Husimi Y. Fine structure in the thermal denaturation of DNA: high temperature-resolution spectrophotometric studies. CRC Crit Rev Biochem. 1980;9(2):87–144. doi: 10.3109/10409238009105432. [DOI] [PubMed] [Google Scholar]
- Wang J. C. Interaction between DNA and an Escherichia coli protein omega. J Mol Biol. 1971 Feb 14;55(3):523–533. doi: 10.1016/0022-2836(71)90334-2. [DOI] [PubMed] [Google Scholar]
- Wang J. C., Peck L. J., Becherer K. DNA supercoiling and its effects on DNA structure and function. Cold Spring Harb Symp Quant Biol. 1983;47(Pt 1):85–91. doi: 10.1101/sqb.1983.047.01.011. [DOI] [PubMed] [Google Scholar]
- Wolf B., Hanlon S. Structural transitions of deoxyribonucleic acid in aqueous electrolyte solutions. II. The role of hydration. Biochemistry. 1975 Apr 22;14(8):1661–1670. doi: 10.1021/bi00679a018. [DOI] [PubMed] [Google Scholar]
- Worcel A., Strogatz S., Riley D. Structure of chromatin and the linking number of DNA. Proc Natl Acad Sci U S A. 1981 Mar;78(3):1461–1465. doi: 10.1073/pnas.78.3.1461. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yang J. T., Samejima T. Optical rotatory dispersion and circular dichroism of nucleic acids. Prog Nucleic Acid Res Mol Biol. 1969;9:223–300. doi: 10.1016/s0079-6603(08)60770-9. [DOI] [PubMed] [Google Scholar]
