λ-prophage Induction in Repair-deficient and Wild Type E. Coli Strains by γ-rays and Heavy Ions

References

• Bertany G. Studies of lysogenesis. I. The mode of phage liberation by lysogenic E. coli. Journal of Bacteriology 1951; 62: 301–303
   Google Scholar
• Bailone A., Levine A., Devoret F. Inactivation of λ prophage repressor in vivo. Journal of Molecular Biology 1979; 131: 553–557
   PubMedGoogle Scholar
• Bridges B.A., Mottershead R.P. Gamma ray mutagenesis in a strain of Escherichia coli deficient in DNA polymerase I. Heredity 1972; 29: 203–211
   PubMed Web of Science ®Google Scholar
• Cherevatenko A.P. The apparatus ‘GENOM’ for experiments in radiation biology. Proceedings of the Fifth All-Union Symposium on Microdosimetry, Ust-Narva, USSR 1986, (In Russian)
   Google Scholar
• Christensen R.C., Tobias C.A., Taylor W.D. Heavy ion induced single-and double-strand breaks in φX-174 replicative form DNA. International Journal of Radiation Biology 1972; 22: 457–477
   Web of Science ®Google Scholar
• Cohen P.S., Resnik J., Sussman R. Interaction of single-strand binding protein and RecA protein at the single-stranded DNA site. Journal of Molecular Biology 1983; 167: 901–909
   PubMed Web of Science ®Google Scholar
• Craig N.L., Roberts J.W. E. coli RecA protein-directed cleavage of phage λ repressor requires polynucleotide. Nature 1980; 283: 26–30
   PubMedGoogle Scholar
• Defais M., Fauquet P., Radman M., Errara M. Ultraviolet inactivation and ultraviolet mutagensis of lambda in different genetic systems. Virology 1971; 43: 495–503
   PubMedGoogle Scholar
• Eisen H.A., Fuerst C.R., Siminovich L., Thomas R., Lambert L., Pereira da Silva L., Jacob F. Genetics and physiology of defective lysogeny in K12(lambda): studies of early mutants. Virology 1966; 30: 224–241
   Google Scholar
• Gottesman S. Genetic control of the SOS-system in E. coli. Cell 1981; 23: 1–2
   Google Scholar
• Johnson A.D., Poteete A.R., Lauer G., Sauer R.T., Ackers G.K., Ptashne M. Repressor and cro-cromponents of an efficient molecular switch. Nature 1981; 294: 217–223
   PubMed Web of Science ®Google Scholar
• Kampf G., Tolkendorf E. Relation between DNA double strand breaks, chromosome breaks and cell survival after the influence of radiations of different LET. Studia Biophysica 1980; 78: 1–10
   Google Scholar
• Kozubek S., Krasavin E.A. Cell sensitivity to irradiation and DNA repair processes. II. The cell sensitivity to high LET radiation. Neoplasma 1984; 31: 684–689
   Google Scholar
• Kozubek S., Krasavin E.A., Cherevatenko A.P., Amirtajev K.G., Tokarova B., Bonev M.N. The role of energy distributions of charged particles in the mutagenic radiation action. Proceedings of the Symposium ‘Quantitative Mathematical models in Radiation Biology’, J. Kiefer. Springer Verlag, Berlin 1988; 85–95
   Google Scholar
• Little J.W., Mount D.W. The SOS regulatory system of Escherichia coli. Cell 1982; 20: 11–22
   Google Scholar
• Lu C., Echols H. RecA protein and SOS-correlation of mutagenesis phenotype with binding of mutant RecA protein to duplex DNA and LexA cleavage. Journal of Molecular Biology 1987; 196: 4–4
   Google Scholar
• Marcovich H. Quantitative biological test sensitive to low doses of ionizing radiations. Nature 1954; 174: 796–797
   Google Scholar
• Marcovich H., Latarget R. Radiobiological aspects of the induction of lysogenic bacteria to produce phage with X-ray gamma-ray, and ultraviolet radiations. Advances in Biological and Medicinal Physics 1958; 6: 75–94
   Google Scholar
• Mount D.W.A., Harris A.W., Fuerst C.R., Siminovich L. Mutations in bacteriophage lambda affecting particles morphogenesis. Virology 1968; 35: 134–149
   Google Scholar
• Munson R.J., Bridges B.A. The LET factor in mutagenesis by ionizing radiation. I. Reversion to wild type of a bacteriophage T4 amber mutant. International Journal of Radiation Biology 1973; 24: 257–273
   Web of Science ®Google Scholar
• Phizicky E.M., Roberts J.W. Induction of SOS function: regulation of proteolytic activity of E. coli RecA protein by interaction with DNA and nucleotide triphosphate. Cell 1981; 25: 259–267
   PubMed Web of Science ®Google Scholar
• Pollard E.C., Achey P.M. Induction of radioresistance in Escherichia coli. Biophysical Journal 1975; 15: 1141–1154
   PubMed Web of Science ®Google Scholar
• Pollard E.C., Randall E.P. Studies on the inducible inhibitor of radiation induced DNA degradation of E. coli. Radiation Research 1973; 55: 265–279
   PubMed Web of Science ®Google Scholar
• Pollard E.C., Person S., Rader M., Fluke D.J. Relation of ultraviolet light mutagenesis to a radiation damage inducible system in Escherichia coli. Radiation Research 1977; 72: 519–532
   Google Scholar
• Ritter M.A., Cleaver J.E., Tobias C.A. High LET radiation induce a large proportion of non-rejoining breaks in mammalian cell DNA. Nature 1977; 266: 653–655
   PubMed Web of Science ®Google Scholar
• Roberts J.W., Roberts C.W., Mount D.W. Inactivation and proteolytic cleavage of phage λ repressor in vitro in an ATP-dependent reaction. Proceedings of the National Academy of Sciences, USA 1977; 74: 2283–2287
   PubMed Web of Science ®Google Scholar
• Satta G., Gudas L.J., Pardee A.B. Degradation of E. coli DNA: evidence for limitation in vivo by protein X, the recA gene product. Molecular and General Genetics 1979; 168: 69–80
   Google Scholar
• Shinoura Y., Ise T., Kato T., Glickman B.W. UmuC-mediate misrepair mutagenesis in Escherichia coli: extent and specificity of SOS mutagenesis. Mutation Research 1983; 11: 51–59
   Google Scholar
• Town C.D., Smith K.C., Kaplan H.S. Repair of X-ray damage to bacterial DNA. Current Topics of Radiation Research 1973; 8: 351–399
   PubMedGoogle Scholar
• Walker G.C. Mutagenesis and inducible response to deoxyribonucleic acid damage in Escherichia coli. Microbiological Review 1984; 48: 60–93
   PubMedGoogle Scholar
• Weigle J.J. Induction of mutation in a bacterial virus. Proceedings of the National Academy of Sciences, USA 1953; 39: 628–636
   PubMed Web of Science ®Google Scholar
• West S.C., Powell K.A., Emmerson P.T. recA--dependent inactivation of the lambda repressor in Escherichia coli lysogen by γ-radiation and by tif expression. Molecular and General Genetics 1975; 141: 1–8
   Google Scholar
• Wilkins R.J. Alpha-ray induced breaks in the DNA of Escherichia coli. International Journal of Radiation Biology 1971; 20: 497–500
   Google Scholar
• Williams J.K.G., Shibata T., Radding C.M. Escherichia coli RecA-protein protects single-stranded DNA or gapped duplex DNA from degradation by RecBC DNase. Journal of Biological Chemistry 1981; 256: 7573–7582
   Google Scholar
• Witkin E.M. The radiation sensitivity of E. coli B: An hypothesis relating filament formation and prophage induction. Proceedings of the National Academy of Sciences, USA 1967; 57: 1275–1280
   PubMed Web of Science ®Google Scholar
• Witkin E.M. Thermal enhancement of UV mutability in a tif-1 uvrA derivative of E. coli B/r: evidence that uv mutagenesis depends upon an inducible function. Proceedings of the National Academy of Sciences, USA 1974; 71: 1930–1935
   PubMedGoogle Scholar