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. 1974 Jul;119(1):1–8. doi: 10.1128/jb.119.1.1-8.1974

Genetic Analysis of a Temperature-Resistant Revertant of the Conditional Lethal Escherichia coli Double Mutant polA12 uvrE502

G B Smirnov 1, A S Saenko 2
PMCID: PMC245565  PMID: 4366022

Abstract

Conditional lethality of the Escherichia coli polA12 uvrE502 double mutant may be overcome by a mutation that has been termed polA350. The polA350 mutation restored the polymerizing activity of deoxyribonucleic acid polymerase I at 42 C in the polA12 mutant and partially suppressed ultraviolet (UV) and methylmethane sulfonate sensitivities of the polA12. Mapping experiments have located polA350 between metE and polA12, very close to the latter. The strain carrying polA12 polA350 and recB21 was viable at 42 C. The effects of the recB21 and polA12 polA350 combination on the UV sensitivity were additive. The triple mutant polA12 polA350 uvrE502 was more UV sensitive than the single uvrE502 mutant.

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Selected References

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

  1. Barbour S. D., Nagaishi H., Templin A., Clark A. J. Biochemical and genetic studies of recombination proficiency in Escherichia coli. II. Rec+ revertants caused by indirect suppression of rec- mutations. Proc Natl Acad Sci U S A. 1970 Sep;67(1):128–135. doi: 10.1073/pnas.67.1.128. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cooper P. K., Hanawalt P. C. Role of DNA polymerase I and the rec system in excision-repair in Escherichia coli. Proc Natl Acad Sci U S A. 1972 May;69(5):1156–1160. doi: 10.1073/pnas.69.5.1156. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. De Lucia P., Cairns J. Isolation of an E. coli strain with a mutation affecting DNA polymerase. Nature. 1969 Dec 20;224(5225):1164–1166. doi: 10.1038/2241164a0. [DOI] [PubMed] [Google Scholar]
  4. GORINI L., KAUFMAN H. Selecting bacterial mutants by the penicillin method. Science. 1960 Feb 26;131(3400):604–605. doi: 10.1126/science.131.3400.604. [DOI] [PubMed] [Google Scholar]
  5. Ganesan A. K., Smith K. C. Dark-recovery processes in Escherichia coli irradiated with ultraviolet light. 3. Effect of rec mutations on recovery of excision-deficient mutants of Escherichia coli K-12. J Bacteriol. 1970 May;102(2):404–410. doi: 10.1128/jb.102.2.404-410.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Gross J. D., Grunstein J., Witkin E. M. Inviability of recA- derivatives of the DNA polymerase mutant of De Lucia and Cairns. J Mol Biol. 1971 Jun 14;58(2):631–634. doi: 10.1016/0022-2836(71)90377-9. [DOI] [PubMed] [Google Scholar]
  7. Gross J., Gross M. Genetic analysis of an E. coli strain with a mutation affecting DNA polymerase. Nature. 1969 Dec 20;224(5225):1166–1168. doi: 10.1038/2241166a0. [DOI] [PubMed] [Google Scholar]
  8. Kanner L., Hanawalt P. Repair deficiency in a bacterial mutant defective in DNA polymerase. Biochem Biophys Res Commun. 1970 Apr 8;39(1):149–155. doi: 10.1016/0006-291x(70)90770-9. [DOI] [PubMed] [Google Scholar]
  9. Kato T. Excision repair characteristics of recB - res - and uvrC - strains of Escherichia coli. J Bacteriol. 1972 Dec;112(3):1237–1246. doi: 10.1128/jb.112.3.1237-1246.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Kushner S. R., Nagaishi H., Templin A., Clark A. J. Genetic recombination in Escherichia coli: the role of exonuclease I. Proc Natl Acad Sci U S A. 1971 Apr;68(4):824–827. doi: 10.1073/pnas.68.4.824. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Monk M., Kinross J. Conditional lethality of recA and recB derivatives of a strain of Escherichia coli K-12 with a temperature-sensitive deoxyribonucleic acid polymerase I. J Bacteriol. 1972 Mar;109(3):971–978. doi: 10.1128/jb.109.3.971-978.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Monk M., Peacey M., Gross J. D. Repair of damage induced by ultraviolet light in DNA polymerase-defective Escherichia coli cells. J Mol Biol. 1971 Jun 14;58(2):623–630. doi: 10.1016/0022-2836(71)90376-7. [DOI] [PubMed] [Google Scholar]
  13. Paterson M. C., Boyle J. M., Setlow R. B. Ultraviolet- and X-ray-induced responses of a deoxyribonucleic acid polymerase-deficient mutant of Escherichia coli. J Bacteriol. 1971 Jul;107(1):61–67. doi: 10.1128/jb.107.1.61-67.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Shizuya H., Dykhuizen D. Conditional lethality of deletions which include uvrB in strains of Escherichia coli lacking deoxyribonucleic acid polymerase I. J Bacteriol. 1972 Nov;112(2):676–681. doi: 10.1128/jb.112.2.676-681.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Shlaes D. M., Anderson J. A., Barbour S. D. Excision repair properties of isogenic rec mutants of Escherichia coli K-12. J Bacteriol. 1972 Sep;111(3):723–730. doi: 10.1128/jb.111.3.723-730.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Siegel E. C. Ultraviolet-sensitive mutator mutU4 of Escherichia coli inviable with polA. J Bacteriol. 1973 Jan;113(1):161–166. doi: 10.1128/jb.113.1.161-166.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Sinzinis B. I., Smirnov G. B., Saenko A. A. Repair deficiency in Escherichia coli UV-sensitive mutator strain uvr502. Biochem Biophys Res Commun. 1973 Jul 2;53(1):309–316. doi: 10.1016/0006-291x(73)91435-6. [DOI] [PubMed] [Google Scholar]
  18. Smirnov G. B., Favorskaya Y. N., Skavronskaya A. G. Monofunctional alkylating agent-induced inactivation, mutagenesis and DNA degradation in an Escherichia coli mutant deficient in DNA polymerase. Mol Gen Genet. 1971;111(4):357–367. doi: 10.1007/BF00569788. [DOI] [PubMed] [Google Scholar]
  19. Smirnov G. B., Filkova E. V., Skavronskaya A. G., Saenko A. S., Sinzinis B. I. Loss and restoration of viability of E. coli due to combinations of mutations affecting DNA polymerase I and repair activities. Mol Gen Genet. 1973 Mar 1;121(2):139–150. doi: 10.1007/BF00277528. [DOI] [PubMed] [Google Scholar]
  20. Smirnov G. B., Filkova E. V., Skavronskaya A. G. The mutator property of uvr502 mutation affecting UV sensitivity of Escherichia coli. Mol Gen Genet. 1972;118(1):51–56. doi: 10.1007/BF02428332. [DOI] [PubMed] [Google Scholar]
  21. Smirnov G. B., Filkova E. V., Skavronskaya A. G. Ultraviolet sensitivity, spontaneous mutability and DNA degradation in Escherichia coli strains carrying mutations in uvr and rec genes. J Gen Microbiol. 1973 Jun;76(2):407–416. doi: 10.1099/00221287-76-2-407. [DOI] [PubMed] [Google Scholar]
  22. Smirnov G. B., Skavronskaya A. G. Location of uvr502 mutation on the chromosome of Escherichia coli K-12. Mol Gen Genet. 1971;113(3):217–221. doi: 10.1007/BF00339541. [DOI] [PubMed] [Google Scholar]
  23. Strike P., Emmerson P. T. [Coexistence of polA and recB mutations of Escherichia coli in the presence of sbc, a mutation which indirectly suppresses recB]. Mol Gen Genet. 1972;116(2):177–180. doi: 10.1007/BF00582226. [DOI] [PubMed] [Google Scholar]
  24. Youngs D. A., Smith K. C. Evidence for the control by exrA and polA genes of two branches of the uvr gene-dependent excision repair pathway in Escherichia coli K-12. J Bacteriol. 1973 Oct;116(1):175–182. doi: 10.1128/jb.116.1.175-182.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]

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