Catabolite repression of SOS-dependent and SOS-independent spontaneous mutagenesis in stationary-phase Escherichia coli

Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis

Volumn 686, Issue 1-2, 2010, Pages 84-89

  MacPhee, D G ^a   Ambrose, M ^b  

^a LA TROBE UNIVERSITY   (Australia)

^b UNIVERSITY OF AUCKLAND   (New Zealand)

Author keywords

Catabolite repression; SOS response; Spontaneous mutagenesis; Stationary phase

Indexed keywords

ALPHA METHYLGLUCOSIDE; BACTERIAL PROTEIN; CARBON; GLYCEROL; LACTOSE; PROTEIN DINB; PROTEIN UMUDC; RECA PROTEIN; UNCLASSIFIED DRUG; VALINE;

ALLELE; ARTICLE; BACTERIAL CELL; BACTERIAL MUTATION; BACTERIAL STRAIN; BACTERIUM CULTURE; BACTERIUM MUTANT; CATABOLITE REPRESSION; CONTROLLED STUDY; ESCHERICHIA COLI; MUTAGENESIS; NONHUMAN; PRIORITY JOURNAL;

BACTERIAL PROTEINS; ESCHERICHIA COLI; GLUCOSE; LACTOSE; MUTAGENESIS; REPRESSOR PROTEINS; SOS RESPONSE (GENETICS);

BACTERIA (MICROORGANISMS); ESCHERICHIA COLI;

EID: 77649190844     PISSN: 00275107     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mrfmmm.2010.01.022     Document Type: Article

References (40)

1. Ambrose M., and MacPhee D.G. Catabolite repressors are potent antimutagens in Escherichia coli plate incorporation assays: experiments with glucose, glucose-6-phosphate and methyl-α-d-glucopyranoside. Mutat. Res. 398 (1998) 175-182
2. Saier Jr. M.H., and Feucht B.U. Coordinate regulation of adenylate cyclase and carbohydrate permeases by the phosphoenolpyruvate: sugar phosphotransferase system in Salmonella typhimurium. J. Biol. Chem. 250 (1975) 7078-7080
3. Epstein W., Rothman-Denes L.B., and Hesse J. Adenosine 3′:5′-cyclic monophosphate as mediator of catabolite repression in Escherichia coli. Proc. Natl. Acad. Sci. U.S.A. 72 (1975) 2300-2304
4. Castro L., Feucht B.U., Morse M.L., and Saier Jr. M.H. Regulation of carbohydrate permeases and adenylate cyclase in Escherichia coli. J. Biol. Chem. 251 (1976) 5522-5527
5. Harwood J.P., Gazdar C., Prasad C., and Peterkofsky A. Involvement of the glucose enzymes II of the sugar phosphotransferase system in the regulation of adenylate cyclase by glucose in Escherichia coli. J. Biol. Chem. 251 (1976) 2462-2468
6. Dumay V., Danchin A., and Crasnier M. Regulation of Escherichia coli adenylate cyclase activity during hexose phosphate transport. Microbiology 142 (1996) 575-583
7. Little J.W., Mount D.W., and Yanisch-Perron C.R. Purified LexA protein is a repressor of the recA and lexA genes. Proc. Natl. Acad. Sci. U.S.A. 78 (1981) 4199-4203
8. Little J.W., and Mount D.W. The SOS regulatory system of Escherichia coli. Cell 29 (1982) 11-22
9. Friedberg E.C., Walker G.C., and Siede W. DNA Repair and Mutagenesis (1995), ASM Press, Washington, DC pp. 407-464
10. Lin L.L., and Little J.W. Isolation and characterization of noncleavable (Ind-) mutants of the LexA repressor of Escherichia coli K-12. J. Bacteriol. 170 (1988) 2163-2173
11. Wagner J., Gruz P., Su-Ryang K., Yamada M., Matsui K., Fuchs R.P.P., and Nohmi T. The dinB gene encodes a novel E. coli DNA polymerase, DNA pol IV, involved in mutagenesis. Mol. Cell 4 (1999) 281-286
12. Tang M., Shen X., Frank E.G., O'Donnell M., Woodgate R., and Goodman M.F. UmuD′(2)C is an error-prone DNA polymerase, Escherichia coli pol V. Proc. Natl. Acad. Sci. U.S.A. 96 (1999) 8919-8924
13. Brotcorne-Lannoye A., and Maenhaut-Michel G. Role of RecA protein in untargeted UV mutagenesis of bacteriophage lambda: evidence for the requirement for the dinB gene. Proc. Natl. Acad. Sci. U.S.A. 83 (1986) 3904-3908
14. Miller J.H. A Short Course in Bacterial Genetics (1992), Cold Spring Harbor Laboratory Press, Plainview, New York
15. Sambrook J., Fritsch E.F., and Maniatis T. Molecular Cloning: A Laboratory Manual. second ed. (1989), Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York
16. Vogel H.J., and Bonner D.M. Acetylornithinase of Escherichia coli: partial purification and some properties. J. Biol. Chem. 218 (1956) 97-106
17. Demerec M., and Cahn E. Studies on mutability in nutritionally deficient strains of Escherichia coli. J. Bacteriol. 65 (1953) 27-36
18. + reversion in Escherichia coli. Mutat. Res. 38 (1976) 3-32
19. Mortelmans K.E., and Stocker B.A.D. Ultraviolet light protection, enhancement of ultraviolet light mutagenesis, and mutator effect of plasmid R46 in Salmonella typhimurium. J. Bacteriol. 128 (1976) 271-282
20. MacPhee D.G. Indications that mutagenesis in Salmonella may be subject to catabolite repression. Mutat. Res. 151 1985 (1985) 35-41
21. Cairns J., and Foster P.L. Adaptive reversion of a frameshift mutation in Escherichia coli. Genetics 128 (1991) 695-701
22. Rosenberg S.M., Longerich S., Gee P., and Harris R.S. Adaptive mutation by deletions in small mononucleotide repeats. Science 265 (1994) 405-407
23. Foster P.L., and Trimarchi J.M. Adaptive reversion of a frameshift mutation in Escherichia coli by simple base deletions in homopolymeric runs. Science 265 (1994) 407-409
24. Taddei F., Matic I., and Radman M. cAMP-dependent SOS induction and mutagenesis is resting bacterial populations. Proc. Natl. Acad. Sci. U.S.A. 92 (1995) 11736-11740
25. McKenzie G.J., Harris R.S., Lee P.L., and Rosenberg S.M. The SOS response regulates adaptive mutation. Proc. Natl. Acad. Sci. U.S.A. 97 (2000) 6646-6651
26. McKenzie G.J., Lee P.L., Lombardo M.J., Hastings P.J., and Rosenberg S.M. SOS mutator DNA polymerse IV functions in adaptive mutation and not adaptive amplication. Mol. Cell 7 (2001) 571-579
27. Layton J.C., and Foster P.L. Error-prone DNA polymerase IV is controlled by the stress-response sigma factor, RpoS, in Escherichia coli. Mol. Microbiol. 50 (2003) 549-561
28. Kim S.R., Maenhaut-Michel G., Yamada M., Yamamoto Y., Matsui K., Sofuni T., Nohmi T., and Omori H. Multiple pathways for SOS-induced mutagenesis in Escherichia coli: an overexpression of dinB/dinP results in strongly enhancing mutagenesis in the absence of any exogenous treatment to damage DNA. Proc. Natl. Acad. Sci. U.S.A. 94 (1997) 13792-13797
29. Galhardo R.S., Do R., Yamada M., Friedberg E.C., Hastings P.J., Nohmi T., and Rosenberg S.M. DinB upregulation is the sole role of the SOS response in stress-induced mutagenesis in Escherichia coli. Genetics 182 (2009) 55-68
30. S (RpoS) subunit of RNA polymerase. Microbiol. Mol. Biol. Rev. 66 (2002) 373-395
31. McCann M.P., Fraley C.D., and Matin A. The putative σ factor KatF is regulated posttranscriptionally during carbon starvation. J. Bacteriol. 175 (1993) 2143-2149
32. Glover S.W. Valine-resistant mutants of Escherichia coli K-12. Genet. Res. 3 (1962) 448-460
33. Cairns J., Overbaugh J., and Miller S. The origin of mutants. Nature (London) 335 (1988) 142-145
34. Schaaper R.M., and Dunn R.L. The antimutator phenotype of E. coli mud is only apparent and results from delayed appearance of mutants. Mutat. Res. 480-481 (2001) 71-75
35. Palejwala V.A., Pandya G.A., Bhanot O.S., Solomon J.J., Murphy H.S., Dunman P.M., and Humayun M.Z. UVM, an ultraviolet-inducible RecA-independent mutagenic phenomenon in Escherichia coli. J. Biol. Chem. 269 (1994) 27433-27440
36. Palejwala V.A., Wang G.E., Murphy H.S., and Humayun M.Z. Functional recA, lexA, umuD, umuC, polA, and polB genes are not required for the Escherichia coli UVM response. J. Bacteriol. 177 (1995) 6041-6048
37. Wang G., Palejwala V.A., Dunman P.M., Aviv D.H., Murphy H.S., Rahman M.S., and Humayun M.Z. Alkylating agents induce UVM, a recA-independent inducible mutagenic phenomenon in Escherichia coli. Genetics 141 (1995) 813-823
38. Wang G., and Humayun M.Z. Induction of the Escherichia coli UVM response by oxidative stress. Mol. Gen. Genet. 251 (1996) 573-579
39. Thomas S.M., and MacPhee D.G. Frameshift mutagenesis by 9-aminoacridine and ICR191 in Escherichia coli: effects of uvrB, recA and lexA mutations and of plasmid pKM101. Mutat. Res. 151 (1985) 49-56
40. Thomas S.M., and MacPhee D.G. RecA-independent mutagenesis in Escherichia coli may be subject to glucose repression. Mutat. Res. 180 (1987) 67-73