Literature DB >> 3888960

Regulation of the SOS response analyzed by RecA protein amplification.

P Calsou, B Salles.   

Abstract

A split UV light dose procedure was used in Escherichia coli to induce an SOS function, RecA protein amplification, which was measured by an immunoradiometric assay. The SOS system was partially induced after the first UV irradiation, and the inducing effects of subsequent identical UV doses were quantified. Variations in the inducing effects of successive UV doses were related to modulations of the SOS signal level during SOS induction. A reduction in the level of SOS signal was found after 20 min in the wild-type strain, hypothesized to result from negative control of repair functions. A few DNA repair mutants were tested by the same procedure; the uvrA, recF, and umuC genes were involved in SOS induction control, but we found differences in their respective kinetics of expression. On the contrary, in a recB mutant, only a slight effect was obtained on this control.

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Year:  1985        PMID: 3888960      PMCID: PMC215898          DOI: 10.1128/jb.162.3.1162-1165.1985

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  21 in total

1.  Suppressibility of recA, recB, and recC mutations by nonsense suppressors.

Authors:  A Templin; L Margossian; A J Clark
Journal:  J Bacteriol       Date:  1978-05       Impact factor: 3.490

2.  Isolation and characterization of mutants of Escherichia coli deficient in induction of mutations by ultraviolet light.

Authors:  T Kato; Y Shinoura
Journal:  Mol Gen Genet       Date:  1977-11-14

Review 3.  Pedigrees of some mutant strains of Escherichia coli K-12.

Authors:  B J Bachmann
Journal:  Bacteriol Rev       Date:  1972-12

Review 4.  Ultraviolet mutagenesis and inducible DNA repair in Escherichia coli.

Authors:  E M Witkin
Journal:  Bacteriol Rev       Date:  1976-12

5.  Mutagenic repair in Escherichia coli. X. The umuC gene product may be required for replication past pyrimidine dimers but not for the coding error in UV-mutagenesis.

Authors:  B A Bridges; R Woodgate
Journal:  Mol Gen Genet       Date:  1984

Review 6.  The SOS regulatory system of Escherichia coli.

Authors:  J W Little; D W Mount
Journal:  Cell       Date:  1982-05       Impact factor: 41.582

7.  An immunoradiometric quantitative assay of Escherichia coli recA protein.

Authors:  C Paoletti; B Salles; P Giacomoni
Journal:  Biochimie       Date:  1982-04       Impact factor: 4.079

8.  The lexA gene product represses its own promoter.

Authors:  R Brent; M Ptashne
Journal:  Proc Natl Acad Sci U S A       Date:  1980-04       Impact factor: 11.205

9.  Inducibility of a gene product required for UV and chemical mutagenesis in Escherichia coli.

Authors:  A Bagg; C J Kenyon; G C Walker
Journal:  Proc Natl Acad Sci U S A       Date:  1981-09       Impact factor: 11.205

Review 10.  Recombination deficient mutants of E. coli and other bacteria.

Authors:  A J Clark
Journal:  Annu Rev Genet       Date:  1973       Impact factor: 16.830

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  3 in total

1.  Weigle reactivation and mutagenesis of bacteriophage lambda in lexA(Def) mutants of E. coli K12.

Authors:  P Calsou; M Defais
Journal:  Mol Gen Genet       Date:  1985

2.  Activated RecA protein may induce expression of a gene that is not controlled by the LexA repressor and whose function is required for mutagenesis and repair of UV-irradiated bacteriophage lambda.

Authors:  P Calsou; A Villaverde; M Defais
Journal:  J Bacteriol       Date:  1987-10       Impact factor: 3.490

3.  Accumulation of inorganic polyphosphate enables stress endurance and catalytic vigour in Pseudomonas putida KT2440.

Authors:  Pablo I Nikel; Max Chavarría; Esteban Martínez-García; Anne C Taylor; Víctor de Lorenzo
Journal:  Microb Cell Fact       Date:  2013-05-20       Impact factor: 5.328

  3 in total

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