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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1977 Jul;74(7):2958–2962. doi: 10.1073/pnas.74.7.2958

Specific action of T4 endonuclease V on damaged DNA in xeroderma pigmentosum cells in vivo.

K Tanaka, H Hayakawa, M Sekiguchi, Y Okada
PMCID: PMC431362  PMID: 197527

Abstract

The specific action of T4 endonuclease V on damaged DNA in xeroderma pigmentosum cells was examined using an in vivo assay system with hemagglutinating virus of Japan (Sendai virus) inactivated by UV light. A clear dose response was observed between the level of UV-induce unscheduled DNA synthesis of xeroderma pigmentosum cells and the amount of T4 endonuclease V activity added. The T4 enzyme was unstable in human cells, and its half-life was 3 hr. Fractions derived from an extract of Escherichia coli infected with T4V1, a mutant defective in the endonuclease V gene, showed no ability to restore the UV-induced unscheduled DNA synthesis of xeroderma pigmentosum cells. However, fractions derived from an extract of T4D-infected E. coli with endonuclease V activity were effective. The T4 enzyme was effective in xeroderma pigmentosum cells on DNA damaged by UV light but not in cells damaged by 4-nitroquinoline 1-oxide. The results of these experiments show that the T4 enzyme has a specific action on human cell DNA in vivo. Treatment with the T4 enzyme increased the survival of group A xeroderma pigmentosum cells after UV irradiation.

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Selected References

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  1. Cleaver J. E., Bootsma D. Xeroderma pigmentosum: biochemical and genetic characteristics. Annu Rev Genet. 1975;9:19–38. doi: 10.1146/annurev.ge.09.120175.000315. [DOI] [PubMed] [Google Scholar]
  2. Day R. S., 3rd Human cells repair DNA damaged by nitrous acid. Mutat Res. 1975 Mar;27(3):407–409. doi: 10.1016/0027-5107(75)90298-5. [DOI] [PubMed] [Google Scholar]
  3. Edenberg H. J., Hanawalt P. C. The timecourse of DNA repair replication in ultraviolet-irradiated HeLa cells. Biochim Biophys Acta. 1973 Oct 12;324(2):206–217. doi: 10.1016/0005-2787(73)90138-x. [DOI] [PubMed] [Google Scholar]
  4. Epstein J. H., Fukuyama K., Reed W. B., Epstein W. L. Defect in DNA synthesis in skin of patients with xeroderma pigmentosum demonstrated in vivo. Science. 1970 Jun 19;168(3938):1477–1478. doi: 10.1126/science.168.3938.1477. [DOI] [PubMed] [Google Scholar]
  5. Friedberg E. C. Studies on the substrate specificity of the T 4 excision repair endonuclease. Mutat Res. 1972 Jun;15(2):113–123. doi: 10.1016/0027-5107(72)90024-3. [DOI] [PubMed] [Google Scholar]
  6. Furusawa M., Nishimura T., Yamaizumi M., Okada Y. Injection of foreign substances into single cells by cell fusion. Nature. 1974 May 31;249(456):449–450. doi: 10.1038/249449a0. [DOI] [PubMed] [Google Scholar]
  7. Kraemer K. H., De Weerd-Kastelein E. A., Robbins J. H., Keijzer W., Barrett S. F., Petinga R. A., Bootsma D. Five complementation groups in xeroderma pigmentosum. Mutat Res. 1975 Dec;33(2-3):327–340. doi: 10.1016/0027-5107(75)90208-0. [DOI] [PubMed] [Google Scholar]
  8. Kuhnlein U., Penhoet E. E., Linn S. An altered apurinic DNA endonuclease activity in group A and group D xeroderma pigmentosum fibroblasts. Proc Natl Acad Sci U S A. 1976 Apr;73(4):1169–1173. doi: 10.1073/pnas.73.4.1169. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  10. Lehmann A. R., Kirk-Bell S., Arlett C. F., Paterson M. C., Lohman P. H., de Weerd-Kastelein E. A., Bootsma D. Xeroderma pigmentosum cells with normal levels of excision repair have a defect in DNA synthesis after UV-irradiation. Proc Natl Acad Sci U S A. 1975 Jan;72(1):219–223. doi: 10.1073/pnas.72.1.219. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Lieberman M. W., Dipple A. Removal of bound carcinogen during DNA repair in nondividing human lymphocytes. Cancer Res. 1972 Sep;32(9):1855–1860. [PubMed] [Google Scholar]
  12. Loyter A., Zakai N., Kulka R. G. "Ultramicroinjection" of macromolecules or small particles into animal cells. A new technique based on virus-induced cell fusion. J Cell Biol. 1975 Aug;66(2):292–304. doi: 10.1083/jcb.66.2.292. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Maher V. M., Birch N., Otto J. R., MacCormick J. J. Cytotoxicity of carcinogenic aromatic amides in normal and xeroderma pigmentosum fibroblasts with different DNA repair capabilities. J Natl Cancer Inst. 1975 Jun;54(6):1287–1294. doi: 10.1093/jnci/54.6.1287. [DOI] [PubMed] [Google Scholar]
  14. Nishida Y., Yasuda S., Sekiguchi M. Repair of DNA damaged by methyl methanesulfonate in bacteriophage T4. Biochim Biophys Acta. 1976 Aug 18;442(2):208–215. doi: 10.1016/0005-2787(76)90491-3. [DOI] [PubMed] [Google Scholar]
  15. Okada Y., Koseki I., Kim J., Maeda Y., Hashimoto T. Modification of cell membranes with viral envelopes during fusion of cells with HVJ (Sendai virus). Exp Cell Res. 1975 Jul;93(2):368–378. doi: 10.1016/0014-4827(75)90462-0. [DOI] [PubMed] [Google Scholar]
  16. Papahadjopoulos D., Poste G., Mayhew E. Cellular uptake of cyclic AMP captured within phospholipid vesicles and effect on cell-growth behaviour. Biochim Biophys Acta. 1974 Sep 23;363(3):404–418. doi: 10.1016/0005-2736(74)90079-0. [DOI] [PubMed] [Google Scholar]
  17. Slor H. Induction of unscheduled DNA synthesis by the carcinogen 7-bromomethylbenz(a)anthracene and its removal from the DNA of normal and xeroderma pigmentosum lymphocytes. Mutat Res. 1973 Aug;19(2):231–235. doi: 10.1016/0027-5107(73)90081-x. [DOI] [PubMed] [Google Scholar]
  18. Sutherland B. M., Rice M., Wagner E. K. Xeroderma pigmentosum cells contain low levels of photoreactivating enzyme. Proc Natl Acad Sci U S A. 1975 Jan;72(1):103–107. doi: 10.1073/pnas.72.1.103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Takebe H., Miki Y., Kozuka T., Furuyama J. I., Tanaka K. DNA repair characteristics and skin cancers of xeroderma pigmentosum patients in Japan. Cancer Res. 1977 Feb;37(2):490–495. [PubMed] [Google Scholar]
  20. Tanaka K., Sekiguchi M., Okada Y. Restoration of ultraviolet-induced unscheduled DNA synthesis of xeroderma pigmentosum cells by the concomitant treatment with bacteriophage T4 endonuclease V and HVJ (Sendai virus). Proc Natl Acad Sci U S A. 1975 Oct;72(10):4071–4075. doi: 10.1073/pnas.72.10.4071. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Uchida T., Yamaizumi M., Okada Y. Reassembled HVJ (Sendai virus) envelopes containing non-toxic mutant proteins of diphtheria toxin show toxicity to mouse L cell. Nature. 1977 Apr 28;266(5605):839–840. doi: 10.1038/266839a0. [DOI] [PubMed] [Google Scholar]
  22. Yasuda S., Sekiguchi M. Further purification and characterization of T4 endonuclease V. Biochim Biophys Acta. 1976 Aug 18;442(2):197–207. doi: 10.1016/0005-2787(76)90490-1. [DOI] [PubMed] [Google Scholar]
  23. Yasuda S., Sekiguchi M. Mechanism of repair of DNA in bacteriophage. II. Inability of ultraviolet-sensitive strains of bacteriophage in inducing an enzyme activity to excise pyrimidine dimers. J Mol Biol. 1970 Jan 28;47(2):243–255. doi: 10.1016/0022-2836(70)90343-8. [DOI] [PubMed] [Google Scholar]
  24. Yasuda S., Sekiguchi M. T4 endonuclease involved in repair of DNA. Proc Natl Acad Sci U S A. 1970 Dec;67(4):1839–1845. doi: 10.1073/pnas.67.4.1839. [DOI] [PMC free article] [PubMed] [Google Scholar]

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