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. 1984 Sep 25;12(18):7071–7086. doi: 10.1093/nar/12.18.7071

Changes in site specificity of single-strand-specific endonucleases on supercoiled PM2 DNA with temperature and ionic environment.

D Kowalski
PMCID: PMC320143  PMID: 6091053

Abstract

Mung bean nuclease sites in supercoiled PM2 DNA at neutral pH were located by linearizing the singly-nicked circular DNA product with venom phosphodiesterase followed by restriction endonuclease mapping. The locations of the sites varied with small changes in temperature and in concentration of NaC1 or magnesium ion. Different environmental changes which affect duplex stability in the same direction showed similar effects on the number of sites and in some cases resulted in identical cleavage patterns. Venom phosphodiesterase and P1 nuclease showed cleavage patterns similar to mung bean nuclease under the same environmental conditions and showed similar variations in cleavage patterns when environmental conditions were changed. Relaxed, closed-circular DNA was slowly cleaved at numerous sites whose locations did not vary with environment. Changes in site specificity are likely the result of environmental effects on the conformation of supercoiled DNA as opposed to effects on the single-strand-specific endonucleases themselves.

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Selected References

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  1. 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]
  2. Azorin F., Nordheim A., Rich A. Formation of Z-DNA in negatively supercoiled plasmids is sensitive to small changes in salt concentration within the physiological range. EMBO J. 1983;2(5):649–655. doi: 10.1002/j.1460-2075.1983.tb01479.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bartok K., Denhardt D. T. Site of cleavage of superhelical phiX174 replicative form DNA by the single strand-specific Neurospora crassa endonuclease. J Biol Chem. 1976 Jan 25;251(2):530–535. [PubMed] [Google Scholar]
  4. 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]
  5. 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]
  6. Benham C. J. Theoretical analysis of competitive conformational transitions in torsionally stressed DNA. J Mol Biol. 1981 Jul 25;150(1):43–68. doi: 10.1016/0022-2836(81)90324-7. [DOI] [PubMed] [Google Scholar]
  7. Benham C. J. Torsional stress and local denaturation in supercoiled DNA. Proc Natl Acad Sci U S A. 1979 Aug;76(8):3870–3874. doi: 10.1073/pnas.76.8.3870. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Brack C., Bickle T. A., Yuan R. The relation of single-stranded regions in bacteriophage PM2 supercoiled DNA to the early melting sequences. J Mol Biol. 1975 Aug 25;96(4):693–702. doi: 10.1016/0022-2836(75)90146-1. [DOI] [PubMed] [Google Scholar]
  9. Brack C., Eberle H., Bickle T. A., Yuan R. A map of the sites on bacteriophage PM2 DNA for the restriction endonucleases HindIII and HpaII. J Mol Biol. 1976 Jun 14;104(1):305–309. doi: 10.1016/0022-2836(76)90016-4. [DOI] [PubMed] [Google Scholar]
  10. Dasgupta S., Allison D. P., Snyder C. E., Mitra S. Base-unpaired regions in supercoiled replicative form DNA of coliphage M13. J Biol Chem. 1977 Aug 25;252(16):5916–5923. [PubMed] [Google Scholar]
  11. DeLeys R. J., Jackson D. A. Dye titrations of covalently closed supercoiled DNA analyzed by agarose gel electrophoresis. Biochem Biophys Res Commun. 1976 Mar 22;69(2):446–454. doi: 10.1016/0006-291x(76)90542-8. [DOI] [PubMed] [Google Scholar]
  12. 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]
  13. Gellert M. DNA topoisomerases. Annu Rev Biochem. 1981;50:879–910. doi: 10.1146/annurev.bi.50.070181.004311. [DOI] [PubMed] [Google Scholar]
  14. Gellert M., Mizuuchi K., O'Dea M. H., Ohmori H., Tomizawa J. DNA gyrase and DNA supercoiling. Cold Spring Harb Symp Quant Biol. 1979;43(Pt 1):35–40. doi: 10.1101/sqb.1979.043.01.007. [DOI] [PubMed] [Google Scholar]
  15. Germond J. E., Vogt V. M., Hirt B. Characterization of the single-strand-specific nuclease S1 activity on double-stranded supercoiled polyoma DNA. Eur J Biochem. 1974 Apr 16;43(3):591–600. doi: 10.1111/j.1432-1033.1974.tb03446.x. [DOI] [PubMed] [Google Scholar]
  16. Helling R. B., Goodman H. M., Boyer H. W. Analysis of endonuclease R-EcoRI fragments of DNA from lambdoid bacteriophages and other viruses by agarose-gel electrophoresis. J Virol. 1974 Nov;14(5):1235–1244. doi: 10.1128/jvi.14.5.1235-1244.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Hentschel C. C. Homocopolymer sequences in the spacer of a sea urchin histone gene repeat are sensitive to S1 nuclease. Nature. 1982 Feb 25;295(5851):714–716. doi: 10.1038/295714a0. [DOI] [PubMed] [Google Scholar]
  18. Hsu T. W., Guntaka R. V., Taylor J. M. Specific site of action for single-strand specific nuclease on the double-stranded circular DNA intermediates of an avian RNA tumor virus. J Virol. 1978 Dec;28(3):1015–1017. doi: 10.1128/jvi.28.3.1015-1017.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Kowalski D. A procedure for the quantitation of relaxed closed circular DNA in the presence of superhelical DNA: an improved fluorometric assay for nicking-closing enzyme. Anal Biochem. 1979 Mar;93(2):346–354. doi: 10.1016/s0003-2697(79)80161-x. [DOI] [PubMed] [Google Scholar]
  20. Kowalski D., Kroeker W. D., Laskowski M., Sr Mung bean nuclease I. Physical, chemical, and catalytic properties. Biochemistry. 1976 Oct 5;15(20):4457–4463. doi: 10.1021/bi00665a019. [DOI] [PubMed] [Google Scholar]
  21. Kowalski D., Sanford J. P. Action of mung bean nuclease on supercoiled PM2 DNA. J Biol Chem. 1982 Jul 10;257(13):7820–7825. [PubMed] [Google Scholar]
  22. Larsen A., Weintraub H. An altered DNA conformation detected by S1 nuclease occurs at specific regions in active chick globin chromatin. Cell. 1982 Jun;29(2):609–622. doi: 10.1016/0092-8674(82)90177-5. [DOI] [PubMed] [Google Scholar]
  23. Laskowski M., Sr Purification and properties of venom phosphodiesterase. Methods Enzymol. 1980;65(1):276–284. doi: 10.1016/s0076-6879(80)65037-x. [DOI] [PubMed] [Google Scholar]
  24. Lilley D. M. Hairpin-loop formation by inverted repeats in supercoiled DNA is a local and transmissible property. Nucleic Acids Res. 1981 Mar 25;9(6):1271–1289. doi: 10.1093/nar/9.6.1271. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. 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]
  26. Nordheim A., Lafer E. M., Peck L. J., Wang J. C., Stollar B. D., Rich A. Negatively supercoiled plasmids contain left-handed Z-DNA segments as detected by specific antibody binding. Cell. 1982 Dec;31(2 Pt 1):309–318. doi: 10.1016/0092-8674(82)90124-6. [DOI] [PubMed] [Google Scholar]
  27. Panayotatos N., Wells R. D. Cruciform structures in supercoiled DNA. Nature. 1981 Feb 5;289(5797):466–470. doi: 10.1038/289466a0. [DOI] [PubMed] [Google Scholar]
  28. Parker R. C., Watson R. M., Vinograd J. Mapping of closed circular DNAs by cleavage with restriction endonucleases and calibration by agarose gel electrophoresis. Proc Natl Acad Sci U S A. 1977 Mar;74(3):851–855. doi: 10.1073/pnas.74.3.851. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. 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]
  30. Pritchard A. E., Kowalski D., Laskowski M., Sr An endonuclease activity of venom phosphodiesterase specific for single-stranded and superhelical DNA. J Biol Chem. 1977 Dec 10;252(23):8652–8659. [PubMed] [Google Scholar]
  31. Pritchard A. E., Laskowski M., Sr Discrete fragmnets produced by limited digestion of superhelical PM2 DNA with venom phosphodiesterase. Cleavage sites and mode of generation. J Biol Chem. 1978 Sep 25;253(18):6606–6613. [PubMed] [Google Scholar]
  32. Pritchard A. E., Laskowski M., Sr Specific cleavages inflicted by venom phosphodiesterase on superhelical phiX174 DNA. J Biol Chem. 1978 Nov 25;253(22):7989–7992. [PubMed] [Google Scholar]
  33. Pulleyblank D. E., Shure M., Tang D., Vinograd J., Vosberg H. P. Action of nicking-closing enzyme on supercoiled and nonsupercoiled closed circular DNA: formation of a Boltzmann distribution of topological isomers. Proc Natl Acad Sci U S A. 1975 Nov;72(11):4280–4284. doi: 10.1073/pnas.72.11.4280. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Singleton C. K. Effects of salts, temperature, and stem length on supercoil-induced formation of cruciforms. J Biol Chem. 1983 Jun 25;258(12):7661–7668. [PubMed] [Google Scholar]
  35. Singleton C. K., Klysik J., Stirdivant S. M., Wells R. D. Left-handed Z-DNA is induced by supercoiling in physiological ionic conditions. Nature. 1982 Sep 23;299(5881):312–316. doi: 10.1038/299312a0. [DOI] [PubMed] [Google Scholar]
  36. Sutcliffe J. G. pBR322 restriction map derived from the DNA sequence: accurate DNA size markers up to 4361 nucleotide pairs long. Nucleic Acids Res. 1978 Aug;5(8):2721–2728. doi: 10.1093/nar/5.8.2721. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Upholt W. B., Gray H. B., Jr, Vinograd J. Sedimentation velocity behavior of closed circular SV40 DNA as a function of superhelix density, ionic strength, counterion and temperature. J Mol Biol. 1971 Nov 28;62(1):21–38. doi: 10.1016/0022-2836(71)90128-8. [DOI] [PubMed] [Google Scholar]
  38. Vollenweider H. J., Koller T., Parello J., Sogo J. M. Superstructure of linear duplex DNA. Proc Natl Acad Sci U S A. 1976 Nov;73(11):4125–4129. doi: 10.1073/pnas.73.11.4125. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Waldeck W., Chowdhury K., Gruss P., Sauer G. Random cleavage of superhelical SV 40 DNA S1 nuclease. Biochim Biophys Acta. 1976 Mar 4;425(2):157–167. doi: 10.1016/0005-2787(76)90021-6. [DOI] [PubMed] [Google Scholar]
  40. Wang J. C. Variation of the average rotation angle of the DNA helix and the superhelical turns of covalently closed cyclic lambda DNA. J Mol Biol. 1969 Jul 14;43(1):25–39. doi: 10.1016/0022-2836(69)90076-x. [DOI] [PubMed] [Google Scholar]
  41. Wells R. D., Goodman T. C., Hillen W., Horn G. T., Klein R. D., Larson J. E., Müller U. R., Neuendorf S. K., Panayotatos N., Stirdivant S. M. DNA structure and gene regulation. Prog Nucleic Acid Res Mol Biol. 1980;24:167–267. doi: 10.1016/s0079-6603(08)60674-1. [DOI] [PubMed] [Google Scholar]
  42. Wiegand R. C., Godson G. N., Radding C. M. Specificity of the S1 nuclease from Aspergillus oryzae. J Biol Chem. 1975 Nov 25;250(22):8848–8855. [PubMed] [Google Scholar]

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