Literature DB >> 8389742

Involvement of Escherichia coli FIS protein in maintenance of bacteriophage mu lysogeny by the repressor: control of early transcription and inhibition of transposition.

M Bétermier1, I Poquet, R Alazard, M Chandler.   

Abstract

The Escherichia coli FIS (factor for inversion stimulation) protein has been implicated in assisting bacteriophage Mu repressor, c, in maintaining the lysogenic state under certain conditions. In a fis strain, a temperature-inducible Mucts62 prophage is induced at lower temperatures than in a wild-type host (M. Bétermier, V. Lefrère, C. Koch, R. Alazard, and M. Chandler, Mol. Microbiol. 3:459-468, 1989). Increasing the prophage copy number rendered Mucts62 less sensitive to this effect of the fis mutation, which thus seems to depend critically on the level of repressor activity. The present study also provides evidence that FIS affects the control of Mu gene expression and transposition. As judged by the use of lac transcriptional fusions, repression of early transcription was reduced three- to fourfold in a fis background, and this could be compensated by an increase in cts62 gene copy number. c was also shown to inhibit Mu transposition two- to fourfold less strongly in a fis host. These modulatory effects, however, could not be correlated to sequence-specific binding of FIS to the Mu genome, in particular to the strong site previously identified on the left end. We therefore speculate that a more general function of FIS is responsible for the observed modulation of Mu lysogeny.

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Year:  1993        PMID: 8389742      PMCID: PMC204797          DOI: 10.1128/jb.175.12.3798-3811.1993

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


  65 in total

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Authors:  N P Higgins
Journal:  Trends Biochem Sci       Date:  1992-06       Impact factor: 13.807

2.  Stabilization of bacteriophage Mu repressor-operator complexes by the Escherichia coli integration host factor protein.

Authors:  M J Gama; A Toussaint; N P Higgins
Journal:  Mol Microbiol       Date:  1992-06       Impact factor: 3.501

3.  Escherichia coli integration host factor stabilizes bacteriophage Mu repressor interactions with operator DNA in vitro.

Authors:  R Alazard; M Bétermier; M Chandler
Journal:  Mol Microbiol       Date:  1992-06       Impact factor: 3.501

4.  Methylation regulates the expression of a DNA-modification function encoded by bacteriophage Mu.

Authors:  R Kahmann
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1983

5.  Ner, a cro-like function of bacteriophage Mu.

Authors:  E Van Leerdam; C Karreman; P van de Putte
Journal:  Virology       Date:  1982-11       Impact factor: 3.616

6.  New M13 vectors for cloning.

Authors:  J Messing
Journal:  Methods Enzymol       Date:  1983       Impact factor: 1.600

7.  Cointegrate formation mediated by Tn9. II. Activity of IS1 is modulated by external DNA sequences.

Authors:  M Chandler; D J Galas
Journal:  J Mol Biol       Date:  1983-10-15       Impact factor: 5.469

8.  rho Mutations restore lamB expression in E. coli K12 strains with an inactive malB region.

Authors:  B Colonna; M Hofnung
Journal:  Mol Gen Genet       Date:  1981

9.  E.coli Fis protein activates ribosomal RNA transcription in vitro and in vivo.

Authors:  W Ross; J F Thompson; J T Newlands; R L Gourse
Journal:  EMBO J       Date:  1990-11       Impact factor: 11.598

10.  Point mutations change the thermal denaturation profile of a short DNA fragment containing the lactose control elements. Comparison between experiment and theory.

Authors:  F Schaeffer; A Kolb; H Buc
Journal:  EMBO J       Date:  1982       Impact factor: 11.598

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  8 in total

1.  Stimulation of DNA inversion by FIS: evidence for enhancer-independent contacts with the Gin-gix complex.

Authors:  A Deufel; T Hermann; R Kahmann; G Muskhelishvili
Journal:  Nucleic Acids Res       Date:  1997-10-01       Impact factor: 16.971

2.  Identification of genes negatively regulated by Fis: Fis and RpoS comodulate growth-phase-dependent gene expression in Escherichia coli.

Authors:  J Xu; R C Johnson
Journal:  J Bacteriol       Date:  1995-02       Impact factor: 3.490

3.  Effects of N-terminal deletions of the Escherichia coli protein Fis on growth rate, tRNA(2Ser) expression and cell morphology.

Authors:  L Spaeny-Dekking; L Nilsson; A von Euler; P van de Putte; N Goosen
Journal:  Mol Gen Genet       Date:  1995-01-20

4.  Immunity of replicating Mu to self-integration: a novel mechanism employing MuB protein.

Authors:  Jun Ge; Zheng Lou; Rasika M Harshey
Journal:  Mob DNA       Date:  2010-02-01

Review 5.  Regulation of bacteriophage Mu transposition.

Authors:  A Toussaint; M J Gama; J Laachouch; G Maenhaut-Michel; A Mhammedi-Alaoui
Journal:  Genetica       Date:  1994       Impact factor: 1.082

6.  Sequence, regulation, and functions of fis in Salmonella typhimurium.

Authors:  R Osuna; D Lienau; K T Hughes; R C Johnson
Journal:  J Bacteriol       Date:  1995-04       Impact factor: 3.490

7.  Silencing of toxic gene expression by Fis.

Authors:  Shweta Karambelkar; Ganduri Swapna; Valakunja Nagaraja
Journal:  Nucleic Acids Res       Date:  2012-01-28       Impact factor: 16.971

8.  Transposable prophage Mu is organized as a stable chromosomal domain of E. coli.

Authors:  Rudra P Saha; Zheng Lou; Luke Meng; Rasika M Harshey
Journal:  PLoS Genet       Date:  2013-11-07       Impact factor: 5.917

  8 in total

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