Literature DB >> 6336731

Effect of suppressors of SOS-mediated filamentation on sfiA operon expression in Escherichia coli.

O Huisman, R D'Ari.   

Abstract

In Escherichia coli, the cell division block observed during the SOS response requires the product of the sfiA gene, whose expression is regulated negatively by the LexA repressor and positively by the RecA protease. We have studied the effect on sfiA expression of sfiA, sfiB, infA, and infB mutations, which are known to affect SOS-associated filamentation. To measure sfiA expression in the different strains, we first constructed a lambda transducing phage carrying an sfiA::lac operon fusion. Mutations at the sfiA locus (dominant and recessive) and the sfiB locus (recessive) had no effect on sfiA expression. The mutations tif (at the recA locus) and tsl (at the lexA locus) are known to induce filamentation and a high level of sfiA expression at 42 degrees C. The infB1 mutation, which suppresses filamentation in a tif tsl strain at 42 degrees C, reduced sfiA expression at 42 degrees C in tif tsl infB1 and tsl infB1 strains but not in a tif infB1 strain. The infA3 mutation, which suppresses tif-mediated filamentation, reduced induction of sfiA expression in a tif infA3 strain at 42 degrees C or after UV irradiation. The isolation and characterization of sfiA constitutive strains revealed only lexA-linked mutations in a sfiA-background, suggesting that LexA is the only readily eliminated repressor of the sfiA gene. Nevertheless, the infA and infB mutations could define elements involved in the regulation of sfiA expression.

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Year:  1983        PMID: 6336731      PMCID: PMC217354          DOI: 10.1128/jb.153.1.169-175.1983

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


  30 in total

1.  E. coli K12 inf: a mutant deficient in prophage lambda induction and cell filamentation.

Authors:  A Bailone; M Blanco; R Devoret
Journal:  Mol Gen Genet       Date:  1975

2.  Cell division during inhibition of deoxyribonucleic acid synthesis in Escherichia coli.

Authors:  C E Helmstetter; O Pierucci
Journal:  J Bacteriol       Date:  1968-05       Impact factor: 3.490

3.  The radiation sensitivity of Escherichia coli B: a hypothesis relating filament formation and prophage induction.

Authors:  E M Witkin
Journal:  Proc Natl Acad Sci U S A       Date:  1967-05       Impact factor: 11.205

4.  SOS chromotest, a direct assay of induction of an SOS function in Escherichia coli K-12 to measure genotoxicity.

Authors:  P Quillardet; O Huisman; R D'Ari; M Hofnung
Journal:  Proc Natl Acad Sci U S A       Date:  1982-10       Impact factor: 11.205

Review 5.  The SOS regulatory system of Escherichia coli.

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

6.  Mechanism of action of the lexA gene product.

Authors:  R Brent; M Ptashne
Journal:  Proc Natl Acad Sci U S A       Date:  1981-07       Impact factor: 11.205

7.  Purified lexA protein is a repressor of the recA and lexA genes.

Authors:  J W Little; D W Mount; C R Yanisch-Perron
Journal:  Proc Natl Acad Sci U S A       Date:  1981-07       Impact factor: 11.205

8.  Regulation of deoxyribonucleic acid replication and cell division in Escherichia coli B-r.

Authors:  D J Clark
Journal:  J Bacteriol       Date:  1968-10       Impact factor: 3.490

9.  DNA replication and indirect induction of the SOS response in Escherichia coli.

Authors:  R D'Ari; O Huisman
Journal:  Biochimie       Date:  1982 Aug-Sep       Impact factor: 4.079

10.  Quantitative evaluation of recA gene expression in Escherichia coli.

Authors:  S Casaregola; R D'Ari; O Huisman
Journal:  Mol Gen Genet       Date:  1982
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  29 in total

1.  Cellular responses to postsegregational killing by restriction-modification genes.

Authors:  N Handa; A Ichige; K Kusano; I Kobayashi
Journal:  J Bacteriol       Date:  2000-04       Impact factor: 3.490

2.  YneA, an SOS-induced inhibitor of cell division in Bacillus subtilis, is regulated posttranslationally and requires the transmembrane region for activity.

Authors:  Allison H Mo; William F Burkholder
Journal:  J Bacteriol       Date:  2010-04-16       Impact factor: 3.490

3.  Inhibition of cell division in hupA hupB mutant bacteria lacking HU protein.

Authors:  A M Dri; J Rouviere-Yaniv; P L Moreau
Journal:  J Bacteriol       Date:  1991-05       Impact factor: 3.490

4.  Genetic and morphological characterization of ftsB and nrdB mutants of Escherichia coli.

Authors:  P E Taschner; J G Verest; C L Woldringh
Journal:  J Bacteriol       Date:  1987-01       Impact factor: 3.490

5.  The rep region of pR plasmid regulates the expression of SOS system.

Authors:  P A Battaglia; F Gigliani; L Marcucci; R Elli
Journal:  Mol Gen Genet       Date:  1987-08

6.  A gene encoding an SOS inhibitor is present in different conjugative plasmids.

Authors:  E Golub; A Bailone; R Devoret
Journal:  J Bacteriol       Date:  1988-09       Impact factor: 3.490

7.  Inhibition of the SOS response of Escherichia coli by the Ada protein.

Authors:  J A Vericat; R Guerrero; J Barbé
Journal:  J Bacteriol       Date:  1988-03       Impact factor: 3.490

8.  Only the N-terminal domain of FtsK functions in cell division.

Authors:  G C Draper; N McLennan; K Begg; M Masters; W D Donachie
Journal:  J Bacteriol       Date:  1998-09       Impact factor: 3.490

9.  DNA replication termination in Escherichia coli parB (a dnaG allele), parA, and gyrB mutants affected in DNA distribution.

Authors:  V Norris; T Alliotte; A Jaffé; R D'Ari
Journal:  J Bacteriol       Date:  1986-11       Impact factor: 3.490

10.  Cell-division control in Escherichia coli: specific induction of the SOS function SfiA protein is sufficient to block septation.

Authors:  O Huisman; R D'Ari; S Gottesman
Journal:  Proc Natl Acad Sci U S A       Date:  1984-07       Impact factor: 11.205

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