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. 1974 Jan;13(1):1–8. doi: 10.1128/jvi.13.1.1-8.1974

Biochemical Studies on the χ Mutation of Bacteriophage T4: Differential Inhibition of χ+ and χ DNA Synthesis by Mitomycin C

Kenji Shimizu 1, Mutsuo Sekiguchi 1
PMCID: PMC355251  PMID: 4359423

Abstract

Biochemical studies were carried out to determine the effect of χ mutation on T4 DNA synthesis. The rate and final extent of DNA synthesis are almost the same with T4D- and T4χ-infected cells, although the burst size of T4χ is about one-sixth that of the wild type. The DNA synthesis of T4χ-infected cells is more readily inhibited by mitomycin C than is that of T4 wild type. When mitomycin C was added during active phage growth, DNA synthesis of T4χ halted almost immediately. T4 DNA polymerases isolated from χ+- and χ-infected cells, however, exhibit no difference with regard to their sensitivities to mitomycin C, priming activities with alkylated or ultraviolet light-irradiated templates and other enzymatic properties.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BOLLUM F. J., SETLOW R. B. Ultraviolet inactivation of DNA primer activity. I. Effects of different wavelengths and doses. Biochim Biophys Acta. 1963 Apr 30;68:599–607. doi: 10.1016/0006-3002(63)90189-6. [DOI] [PubMed] [Google Scholar]
  2. BURTON K. A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid. Biochem J. 1956 Feb;62(2):315–323. doi: 10.1042/bj0620315. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Baldy M. W., Strom B., Bernstein H. Repair of alkylated bacteriophage T4 deoxyribonucleic acid by a mechanism involving polynucleotide ligase. J Virol. 1971 Mar;7(3):407–408. doi: 10.1128/jvi.7.3.407-408.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Baldy M. W. The UV sensitivity of some early-function temperature-sensitive mutants of phage T4. Virology. 1970 Feb;40(2):272–287. doi: 10.1016/0042-6822(70)90403-4. [DOI] [PubMed] [Google Scholar]
  5. Boyle J. M., Symonds N. Radiation-sensitive mutants of T4D. I. T4y: a new radiation-sensitive mutant; effect of the mutation on radiation survival, growth and recombination. Mutat Res. 1969 Nov-Dec;8(3):431–439. doi: 10.1016/0027-5107(69)90060-8. [DOI] [PubMed] [Google Scholar]
  6. De Waard A., Paul A. V., Lehman I. R. The structural gene for deoxyribonucleic acid polymerase in bacteriophages T4 and T5. Proc Natl Acad Sci U S A. 1965 Oct;54(4):1241–1248. doi: 10.1073/pnas.54.4.1241. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Drake J. W. The genetic control of spontaneous and induced mutation rates in bacteriophage T4. Genetics. 1973 Apr;73(Suppl):45–64. [PubMed] [Google Scholar]
  8. Friedberg E. C., King J. J. Dark repair of ultraviolet-irradiated deoxyribonucleic acid by bacteriophage T4: purification and characterization of a dimer-specific phage-induced endonuclease. J Bacteriol. 1971 May;106(2):500–507. doi: 10.1128/jb.106.2.500-507.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. 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]
  10. Goulian M., Lucas Z. J., Kornberg A. Enzymatic synthesis of deoxyribonucleic acid. XXV. Purification and properties of deoxyribonucleic acid polymerase induced by infection with phage T4. J Biol Chem. 1968 Feb 10;243(3):627–638. [PubMed] [Google Scholar]
  11. HARM W. Mutants of phage T4 with increased sensitivity to ultraviolet. Virology. 1963 Jan;19:66–71. doi: 10.1016/0042-6822(63)90025-4. [DOI] [PubMed] [Google Scholar]
  12. Harm W. Recovery of UV-inactivated E. coli cells by the v-gene action of phage T4. Mutat Res. 1968 Jul-Aug;6(1):175–179. doi: 10.1016/0027-5107(68)90115-2. [DOI] [PubMed] [Google Scholar]
  13. IYER V. N., SZYBALSKI W. A MOLECULAR MECHANISM OF MITOMYCIN ACTION: LINKING OF COMPLEMENTARY DNA STRANDS. Proc Natl Acad Sci U S A. 1963 Aug;50:355–362. doi: 10.1073/pnas.50.2.355. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. KECK K., MAHLER H. R., FRASER D. Synthesis of deoxycytidine-5'-phosphate deaminase in Escherichia coli infected by T2 bacteriophage. Arch Biochem Biophys. 1960 Jan;86:85–88. doi: 10.1016/0003-9861(60)90373-8. [DOI] [PubMed] [Google Scholar]
  15. 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]
  16. MAGEE W. E., MILLER O. V. Dissociation of the synthesis of host and viral deoxyribonucleic acid. Biochim Biophys Acta. 1962 Jun 11;55:818–826. doi: 10.1016/0006-3002(62)90894-6. [DOI] [PubMed] [Google Scholar]
  17. Otsuji N., Murayama I. Deoxyribonucleic acid damage by monofunctional mitomycins and its repair in Escherichia coli. J Bacteriol. 1972 Feb;109(2):475–483. doi: 10.1128/jb.109.2.475-483.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Poddar R. K., Sinsheimer R. L. Nature of the complementary strands synthesized in vitro upon the single-stranded circular DNA of bacteriophage phiX174 after ultraviolet irradiation. Biophys J. 1971 Apr;11(4):355–369. doi: 10.1016/s0006-3495(71)86220-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Ray U., Bartenstein L., Drake J. W. Inactivation of bacteriophage T4 by ethyl methanesulfonate: influence of host and viral genotypes. J Virol. 1972 Mar;9(3):440–447. doi: 10.1128/jvi.9.3.440-447.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. SEKIGUCHI M., TAKAGI Y. Effect of mitomycin C on the synthesis of bacterial and viral deoxyribonucleic acid. Biochim Biophys Acta. 1960 Jul 15;41:434–443. doi: 10.1016/0006-3002(60)90040-8. [DOI] [PubMed] [Google Scholar]
  21. SHIBA S., TERAWAKI A., TAGUCHI T., KAWAMATA J. Selective inhibition of formation of deoxyribonucleic acid in Escherichia coli by mitomycin C. Nature. 1959 Apr 11;183(4667):1056–1057. doi: 10.1038/1831056a0. [DOI] [PubMed] [Google Scholar]
  22. Sekiguchi M. Studies on the physiological defect in rII mutants of bacteriophage T4. J Mol Biol. 1966 Apr;16(2):503–522. doi: 10.1016/s0022-2836(66)80188-2. [DOI] [PubMed] [Google Scholar]
  23. Smith S. M., Symonds N. The unexpected location of a gene conferring abnormal radiation sensitivity on phage T4. Nature. 1973 Feb 9;241(5389):395–396. doi: 10.1038/241395a0. [DOI] [PubMed] [Google Scholar]
  24. Taketo A., Yasuda S., Sekiguchi M. Initial step of excision repair in Escherichia coli: replacement of defective function of uvr mutants by T4 endonuclease V. J Mol Biol. 1972 Sep 14;70(1):1–14. doi: 10.1016/0022-2836(72)90160-x. [DOI] [PubMed] [Google Scholar]
  25. Wood W. B., Edgar R. S. Building a bacterial virus. Sci Am. 1967 Jul;217(1):61–passim. [PubMed] [Google Scholar]
  26. 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]
  27. van den Ende P., Symonds N. The isolation and characterization of a T4 mutant partially defective in recombination. Mol Gen Genet. 1972;116(3):239–247. doi: 10.1007/BF00269768. [DOI] [PubMed] [Google Scholar]

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