Survival and induction of SOS in Escherichia coli treated with cisplatin, UV-irradiation, or mitomycin C are dependent on the function of the RecBC and RecFOR pathways of homologous recombination

Mutation Research - DNA Repair

Volumn 486, Issue 1, 2001, Pages 21-29

  Keller, Kimberly L ^a   Overbeck Carrick, Terri L ^a   Beck, Doris J ^a  

^a BOWLING GREEN STATE UNIVERSITY   (United States)

Author keywords

Cisplatin; Homologous recombination; Mitomycin C; RecB; RecO; SOS induction

Indexed keywords

CISPLATIN; GALACTOSIDASE; MITOMYCIN C; RECBC PROTEIN; RECFOR PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; CELL SURVIVAL; CONTROLLED STUDY; DNA CROSS LINKING; DNA DAMAGE; DNA REPAIR; DRUG ACTIVITY; ENZYME ACTIVITY; ESCHERICHIA COLI; GENETIC RECOMBINATION; NONHUMAN; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; SOS CHROMOTEST; ULTRAVIOLET IRRADIATION;

BACTERIAL PROTEINS; CELL DIVISION; CISPLATIN; CROSS-LINKING REAGENTS; DNA DAMAGE; DNA REPAIR; DNA-BINDING PROTEINS; DOSE-RESPONSE RELATIONSHIP, DRUG; DOSE-RESPONSE RELATIONSHIP, RADIATION; DRUG RESISTANCE; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; EXODEOXYRIBONUCLEASE V; EXODEOXYRIBONUCLEASES; GENOTYPE; MITOMYCIN; MUTATION; NUCLEIC ACID SYNTHESIS INHIBITORS; PHENOTYPE; RADIATION-SENSITIZING AGENTS; RECOMBINATION, GENETIC; SIGNAL TRANSDUCTION; SOS RESPONSE (GENETICS); ULTRAVIOLET RAYS;

ESCHERICHIA COLI; SULA;

EID: 0035811261     PISSN: 09218777     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0921-8777(01)00077-5     Document Type: Article

References (35)

1. M. Radman, Phenomenology of an inducible mutagenic DNA repair pathway in Escherichia coli: SOS repair hypothesis, in: L. Prakash, F. Sherman, M. Miller, C. Lawrence, H.W. Tabor (Eds.), Molecular and Environmental Aspects of Mutagenesis, Charles C. Thomas, Springfield, IL, pp. 128-142
2. Little J., Mount D. The SOS regulatory system of Escherichia coli. Cell. 29:1982;11-22.
3. Walker G.C. Mutagenesis and inducible responses to DNA damage by Escherichia coli. Microbiol. Rev. 48:1985;60-93.
4. A. Kuzminov, Recombinational Repair of DNA Damage, Chapman & Hall, New York, 1996, pp. 81-89, 122-145.
5. Kowalczykowski S. Initiation of genetic recombination and recombination-dependent replication. TIBS. 25:2000;156-165.
6. Taylor A.F., Smith G.R. Monomeric RecBCD enzyme binds and unwinds DNA. J. Bacteriol. 174:1995;24451-24458.
7. Chadhury A.M., Smith G.R. Role of Escherichia coli RecBC enzyme in SOS induction. Mol. Gen. Genet. 201:1985;525-528.
8. Whitby M.C., Lloyd R.G. Altered SOS induction associated with mutations in recF, recO and recR. Mol. Gen. Genet. 246:1995;174-179.
9. Umezu K., Kolodner R. Biochemical interaction of the Escherichia coli RecF, RecO, and RecR proteins with RecA protein and single-stranded DNA binding protein. Proc. Natl. Acad. Sci. U. S. A. 90:1993;3875-3879.
10. Umezu K., Kolodner R. Protein interactions in genetic recombination in Escherichia coli. J. Biol. Chem. 269:1994;30005-30013.
11. Rosenberg B., VanCamp L., Krigas T. Inhibition of cell division in Escherichia coli by electrolysis products from a platinum electrode. Nature. 205:1965;698-699.
12. Beck D.J., Vazquez D., Cook R. Effect of cis-platinum(II)diamminodichloride on wild type and a recA mutant of Escherichia coli. J. Clin. Hematol. Oncol. 7:1975;726-774.
13. S.K. Carter, Cisplatin - past, present and future, in: M.P. Hacker, E.B. Douple, I.H. Krakoff (Eds.) Platinum Coordination Complexes in Cancer Chemotherapy, Boston, pp. 359-376.
14. Eastman A. The formation, isolation, and characterization of DNA adducts produced by anticancer platinum complexes. Pharmacol. Ther. 34:1987;155-166.
15. Johnson S.W., Swiggard P.A., Handel L.M., Brennan J.M., Godwin A.K., Ozols R.F., Hamilton T.C. Relationship between platinum-DNA adduct formation and removal and cisplatin cytotoxicity in cisplatin-sensitive and -resistant human ovarian cancer cells. Cancer Res. 54:1994;5911-5916.
16. Jarosik G.P., Beck D.J. The effects of cis-platinum(II)diamminochloride, UV light and N-methyl-N-nitro-N-nitrosoguanidine on Escherichia coli: plasmid mediated resistance to mutagens. Chem. Biol. Interact. 51:1984;247-259.
17. Beck D.J., Brubaker R.R. Effect of cisplatinum(II)diamminochloride on wild type and deoxyribonucleic acid repair-deficient mutants of Escherichia coli. J. Bacteriol. 116:1973;1247-1252.
18. Zdraveski Z.Z., Mello J.A., Marinus M.G., Essigmann J.M. Multiple pathways of recombination define cellular responses to cisplatin. Chem. Biol. 7:2000;39-50.
19. Courcelle J., Crowley D.J., Hanawalt P.C. Recovery of DNA replication in UV-irradiated Escherichia coli requires both excision repair and the RecF protein function. J. Bacteriol. 181:1999;916-922.
20. Kumar G.S., Lipman R., Cummings J., Tomasz M. Mitomycin C-DNA adducts generated by DT-diaphorase. Revised mechanism of the enzymatic reductive activation of mitomycin C. Biochemistry. 36:1997;14128-14136.
21. Quillardet P., Hofnung M. The SOS chromotest, a colorimetric bacterial assay for genotoxins: procedures. Mutat. Res. 147:1985;65-78.
22. Quillardet P., Hofnung M. The SOS chromotest: a review. Mutat. Res. 297:1993;235-279.
23. Breña-Valle M., Serment J. SOS Induction by γ-radiation in Escherichia coli strains defective in repair and/or recombination mechanisms. Mutagenesis. 13:1998;637-641.
24. J. Sambrook, E.F. Fritsch, T. Maniatis, in: Molecular Cloning: A Laboratory Manual, 2nd Edition, Cold Spring Harbor Laboratory Press, New York, Vol. 3, 1989, p. A1.
25. Mersch-Sundermann V., Mochayedi S., Kevekordes S. Genotoxicity of polycyclic aromatic hydrocarbons in Escherichia coli. Mutat. Res. 278:1992;1-9.
26. Rupp W.D., Howard-Flanders P. Discontinuities in the DNA synthesized in an excision-defective strain of Escherichia coli following ultraviolet irradiation. J. Mol. Biol. 31:1968;291-304.
27. Beck D.J., Popoff S., Sancar A., Rupp W.D. Reactions of the UVRABC excision nuclease with DNA damaged by diamminedichloroplatinum(II). Nucleic Acids Res. 13:1985;7395-7412.
28. E.C. Friedberg, G.C. Walker, W. Siede, DNA Repair and Mutagenesis, American Society for Microbiology Press, Washington, DC, 1995, pp. 191-232, 440-456.
29. Van Houten B., Gamper H., Holbrook S.R., Hearst J.E., Sancar A. Action mechanism of ABC excision nuclease on a DNA substrate containing a psoralen crosslink at a defined position. Proc. Natl. Acad. Sci. U. S. A. 83:1986;8077-8081.
30. Sancar A., Franklin K.A., Sancar G.B. Escherichia coli DNA photolyase stimulates UvrABC excision nuclease in vitro. Proc. Natl. Acad. Sci. U. S. A. 81:1984;7397-7401.
31. Van Houten B., Cheng S., Chen Y. Measuring gene-specific nucleotide excision repair in human cells using quantitative amplification of long targets from nanogram quantities of DNA. Mutat. Res. 460:2000;81-94.
32. Hegde S., Sandler S.J., Clark A.J., Madiraju M.V.V.S. recO and recR mutations delay induction of the SOS response in Escherichia coli. Mol. Gen. Genet. 246:1995;254-258.
33. Goodman M.F. Coping with replication "train wrecks" in Escherichia coli using Pol V, Pol II and RecA proteins. TIBS. 25:2000;189-195.
34. Barbé J., Vericat J.A., Cairó J., Guerrero R. Further characterization of SOS system induction in recBC mutants of Escherichia coli. Mutat. Res. 146:1985;23-32.
35. Lloyd R., Thomas A. On the nature of the RecBC and RecF pathways of conjugal recombination in Escherichia coli. Mol. Gen. Genet. 190:1982;156-161.