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. 1988 Sep 12;16(17):8277–8289. doi: 10.1093/nar/16.17.8277

Detection of Z DNA binding proteins in tissue culture cells.

I R Leith 1, R T Hay 1, W C Russell 1
PMCID: PMC338558  PMID: 3419919

Abstract

A gel electrophoresis DNA binding assay to detect Z DNA binding proteins has been developed utilising [32P] labelled poly [d(G-C)] which was converted to the Z form by incubation in 100 microM Co(NH3)6Cl3. The parameters of the assay were established using a Z DNA antibody as a model system and then applied to extracts of Hela and BHK21 cells. Using an anti-Z DNA antibody conditions were established which allowed resolution of antibody-DNA complexes and free DNA in the presence of 100 microM Co(NH3)6Cl3. The inclusion of unlabelled complementary homopolymers eliminated non-specific binding to the labelled Z-DNA probe. Competition experiments demonstrated that the assay was highly specific for double stranded non-B DNA. Application of the technique to extracts of mammalian cells demonstrated that human and hamster cells contain Z-DNA binding proteins; further characterisation by a blotting technique indicated that a 56,000 molecular weight cell protein preferentially binds Z-DNA.

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Selected References

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  1. Azorin F., Hahn R., Rich A. Restriction endonucleases can be used to study B-Z junctions in supercoiled DNA. Proc Natl Acad Sci U S A. 1984 Sep;81(18):5714–5718. doi: 10.1073/pnas.81.18.5714. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Azorin F., Rich A. Isolation of Z-DNA binding proteins from SV40 minichromosomes: evidence for binding to the viral control region. Cell. 1985 Jun;41(2):365–374. doi: 10.1016/s0092-8674(85)80009-x. [DOI] [PubMed] [Google Scholar]
  3. Barrett P., Clark L., Hay R. T. A cellular protein binds to a conserved sequence in the adenovirus type 2 enhancer. Nucleic Acids Res. 1987 Mar 25;15(6):2719–2735. doi: 10.1093/nar/15.6.2719. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Barton J. K., Basile L. A., Danishefsky A., Alexandrescu A. Chiral probes for the handedness of DNA helices: enantiomers of tris(4,7-diphenylphenanthroline)ruthenium(II). Proc Natl Acad Sci U S A. 1984 Apr;81(7):1961–1965. doi: 10.1073/pnas.81.7.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. 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]
  6. Blaho J. A., Wells R. D. Left-handed Z-DNA binding by the recA protein of Escherichia coli. J Biol Chem. 1987 May 5;262(13):6082–6088. [PubMed] [Google Scholar]
  7. Fried M., Crothers D. M. Equilibria and kinetics of lac repressor-operator interactions by polyacrylamide gel electrophoresis. Nucleic Acids Res. 1981 Dec 11;9(23):6505–6525. doi: 10.1093/nar/9.23.6505. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Garner M. M., Revzin A. A gel electrophoresis method for quantifying the binding of proteins to specific DNA regions: application to components of the Escherichia coli lactose operon regulatory system. Nucleic Acids Res. 1981 Jul 10;9(13):3047–3060. doi: 10.1093/nar/9.13.3047. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gut S. H., Bischoff M., Hobi R., Kuenzle C. C. Z-DNA-binding proteins from bull testis. Nucleic Acids Res. 1987 Dec 10;15(23):9691–9705. doi: 10.1093/nar/15.23.9691. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hill R. J., Stollar B. D. Dependence of Z-DNA antibody binding to polytene chromosomes on acid fixation and DNA torsional strain. Nature. 1983 Sep 22;305(5932):338–340. doi: 10.1038/305338a0. [DOI] [PubMed] [Google Scholar]
  11. Jaworski A., Hsieh W. T., Blaho J. A., Larson J. E., Wells R. D. Left-handed DNA in vivo. Science. 1987 Nov 6;238(4828):773–777. doi: 10.1126/science.3313728. [DOI] [PubMed] [Google Scholar]
  12. Kitchin P. A., Klein V. A., Ryan K. A., Gann K. L., Rauch C. A., Kang D. S., Wells R. D., Englund P. T. A highly bent fragment of Crithidia fasciculata kinetoplast DNA. J Biol Chem. 1986 Aug 25;261(24):11302–11309. [PubMed] [Google Scholar]
  13. Kmiec E. B., Holloman W. K. Synapsis promoted by Ustilago rec1 protein. Cell. 1984 Mar;36(3):593–598. doi: 10.1016/0092-8674(84)90338-6. [DOI] [PubMed] [Google Scholar]
  14. Lafer E. M., Möller A., Nordheim A., Stollar B. D., Rich A. Antibodies specific for left-handed Z-DNA. Proc Natl Acad Sci U S A. 1981 Jun;78(6):3546–3550. doi: 10.1073/pnas.78.6.3546. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Lafer E. M., Sousa R., Rosen B., Hsu A., Rich A. Isolation and characterization of Z-DNA binding proteins from wheat germ. Biochemistry. 1985 Sep 10;24(19):5070–5076. doi: 10.1021/bi00340a017. [DOI] [PubMed] [Google Scholar]
  16. Lancillotti F., Lopez M. C., Arias P., Alonso C. Z-DNA in transcriptionally active chromosomes. Proc Natl Acad Sci U S A. 1987 Mar;84(6):1560–1564. doi: 10.1073/pnas.84.6.1560. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. 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]
  18. Nelson H. C., Finch J. T., Luisi B. F., Klug A. The structure of an oligo(dA).oligo(dT) tract and its biological implications. Nature. 1987 Nov 19;330(6145):221–226. doi: 10.1038/330221a0. [DOI] [PubMed] [Google Scholar]
  19. Nordheim A., Meese K. Topoisomer gel retardation: detection of anti-Z-DNA antibodies bound to Z-DNA within supercoiled DNA minicircles. Nucleic Acids Res. 1988 Jan 11;16(1):21–37. doi: 10.1093/nar/16.1.21. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Nordheim A., Pardue M. L., Lafer E. M., Möller A., Stollar B. D., Rich A. Antibodies to left-handed Z-DNA bind to interband regions of Drosophila polytene chromosomes. Nature. 1981 Dec 3;294(5840):417–422. doi: 10.1038/294417a0. [DOI] [PubMed] [Google Scholar]
  21. Nordheim A., Tesser P., Azorin F., Kwon Y. H., Möller A., Rich A. Isolation of Drosophila proteins that bind selectively to left-handed Z-DNA. Proc Natl Acad Sci U S A. 1982 Dec;79(24):7729–7733. doi: 10.1073/pnas.79.24.7729. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Rich A., Nordheim A., Wang A. H. The chemistry and biology of left-handed Z-DNA. Annu Rev Biochem. 1984;53:791–846. doi: 10.1146/annurev.bi.53.070184.004043. [DOI] [PubMed] [Google Scholar]
  23. Robert-Nicoud M., Arndt-Jovin D. J., Zarling D. A., Jovin T. M. Immunological detection of left-handed Z DNA in isolated polytene chromosomes. Effects of ionic strength, pH, temperature and topological stress. EMBO J. 1984 Apr;3(4):721–731. doi: 10.1002/j.1460-2075.1984.tb01875.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Russell W. C., Blair G. E. Polypeptide phosphorylation in adenovirus-infected cells. J Gen Virol. 1977 Jan;34(1):19–35. doi: 10.1099/0022-1317-34-1-19. [DOI] [PubMed] [Google Scholar]
  25. Russell W. C., Precious B., Martin S. R., Bayley P. M. Differential promotion and suppression of Z leads to B transitions in poly[d(G-C)] by histone subclasses, polyamino acids and polyamines. EMBO J. 1983;2(10):1647–1653. doi: 10.1002/j.1460-2075.1983.tb01639.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Russell W. C., Precious B. Nucleic acid-binding properties of adenovirus structural polypeptides. J Gen Virol. 1982 Nov;63(Pt 1):69–79. doi: 10.1099/0022-1317-63-1-69. [DOI] [PubMed] [Google Scholar]
  27. Seed B. Diazotizable arylamine cellulose papers for the coupling and hybridization of nucleic acids. Nucleic Acids Res. 1982 Mar 11;10(5):1799–1810. doi: 10.1093/nar/10.5.1799. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Silva C. M., Tully D. B., Petch L. A., Jewell C. M., Cidlowski J. A. Application of a protein-blotting procedure to the study of human glucocorticoid receptor interactions with DNA. Proc Natl Acad Sci U S A. 1987 Apr;84(7):1744–1748. doi: 10.1073/pnas.84.7.1744. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Snyder M., Buchman A. R., Davis R. W. Bent DNA at a yeast autonomously replicating sequence. Nature. 1986 Nov 6;324(6092):87–89. doi: 10.1038/324087a0. [DOI] [PubMed] [Google Scholar]
  30. Soslau G., Parker J., Nelson J. W. Methylation and restriction endonuclease cleavage of linear Z-DNA in the presence of hexamminecobalt (III) ions. Nucleic Acids Res. 1986 Sep 25;14(18):7237–7252. doi: 10.1093/nar/14.18.7237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Stenzel T. T., Patel P., Bastia D. The integration host factor of Escherichia coli binds to bent DNA at the origin of replication of the plasmid pSC101. Cell. 1987 Jun 5;49(5):709–717. doi: 10.1016/0092-8674(87)90547-2. [DOI] [PubMed] [Google Scholar]
  32. Viegas-Péquignot E., Derbin C., Malfoy B., Taillandier E., Leng M., Dutrillaux B. Z-DNA immunoreactivity in fixed metaphase chromosomes of primates. Proc Natl Acad Sci U S A. 1983 Oct;80(19):5890–5894. doi: 10.1073/pnas.80.19.5890. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Wells R. D. Biophysics of left-handed Z-DNA. Adv Biophys. 1985;20:31–38. doi: 10.1016/0065-227x(85)90029-2. [DOI] [PubMed] [Google Scholar]
  34. Zahn K., Blattner F. R. Direct evidence for DNA bending at the lambda replication origin. Science. 1987 Apr 24;236(4800):416–422. doi: 10.1126/science.2951850. [DOI] [PubMed] [Google Scholar]

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