Literature DB >> 7928948

Response to UV damage by four Escherichia coli K-12 restriction systems.

J E Kelleher1, E A Raleigh.   

Abstract

To understand the role of restriction in regulating gene flow in bacterial populations, we would like to understand the regulation of restriction enzyme activity. Several antirestriction (restriction alleviation) systems are known that reduce the activity of type I restriction enzymes like EcoKI in vivo. Most of these do not act on type II or type III enzymes, but little information is available for the unclassified modification-dependent systems, of which there are three in E. coli K-12. Of particular interest are two physiological controls on type I enzymes: EcoKI restriction is reduced 2 to 3 orders of magnitude following DNA damage, and a similar effect is seen constitutively in Dam- cells. We used the behavior of EcoKI as a control for testing the response to UV treatment of the three endogenous modification-dependent restriction systems of K-12, McrA, McrBC, and Mrr. Two of these were also tested for response to Dam status. We find that all four resident restriction systems show reduced activity following UV treatment, but not in a unified fashion; each response was genetically and physiologically distinct. Possible mechanisms are discussed.

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Year:  1994        PMID: 7928948      PMCID: PMC196804          DOI: 10.1128/jb.176.19.5888-5896.1994

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


  75 in total

1.  Genetic and sequence organization of the mcrBC locus of Escherichia coli K-12.

Authors:  D Dila; E Sutherland; L Moran; B Slatko; E A Raleigh
Journal:  J Bacteriol       Date:  1990-09       Impact factor: 3.490

2.  The role of dam methyltransferase in the control of DNA replication in E. coli.

Authors:  E Boye; A Løbner-Olesen
Journal:  Cell       Date:  1990-09-07       Impact factor: 41.582

3.  Nomenclature relating to restriction of modified DNA in Escherichia coli.

Authors:  E A Raleigh; J Benner; F Bloom; H D Braymer; E DeCruz; K Dharmalingam; J Heitman; M Noyer Weidner; A Piekarowicz; P L Kretz
Journal:  J Bacteriol       Date:  1991-04       Impact factor: 3.490

4.  Nature of the SOS-inducing signal in Escherichia coli. The involvement of DNA replication.

Authors:  M Sassanfar; J W Roberts
Journal:  J Mol Biol       Date:  1990-03-05       Impact factor: 5.469

5.  Genetic and physical mapping of the mcrA (rglA) and mcrB (rglB) loci of Escherichia coli K-12.

Authors:  E A Raleigh; R Trimarchi; H Revel
Journal:  Genetics       Date:  1989-06       Impact factor: 4.562

Review 6.  A possible role for DNA restriction in bacterial evolution.

Authors:  C Price; T A Bickle
Journal:  Microbiol Sci       Date:  1986-10

7.  Genetic and physical mapping of recF in Escherichia coli K-12.

Authors:  L W Ream; L Margossian; A J Clark; F G Hansen; K von Meyenburg
Journal:  Mol Gen Genet       Date:  1980

8.  Control of recA gene RNA in E. coli: regulatory and signal genes.

Authors:  A McPartland; L Green; H Echols
Journal:  Cell       Date:  1980-07       Impact factor: 41.582

Review 9.  The great GATC: DNA methylation in E. coli.

Authors:  F Barras; M G Marinus
Journal:  Trends Genet       Date:  1989-05       Impact factor: 11.639

10.  Efficient transformation of Bacillus thuringiensis requires nonmethylated plasmid DNA.

Authors:  A Macaluso; A M Mettus
Journal:  J Bacteriol       Date:  1991-02       Impact factor: 3.490

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  18 in total

1.  Regulation of endonuclease activity by proteolysis prevents breakage of unmodified bacterial chromosomes by type I restriction enzymes.

Authors:  S Makovets; V A Doronina; N E Murray
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-17       Impact factor: 11.205

Review 2.  Type I restriction systems: sophisticated molecular machines (a legacy of Bertani and Weigle).

Authors:  N E Murray
Journal:  Microbiol Mol Biol Rev       Date:  2000-06       Impact factor: 11.056

Review 3.  Stress-induced evolution and the biosafety of genetically modified microorganisms released into the environment.

Authors:  V V Velkov
Journal:  J Biosci       Date:  2001-12       Impact factor: 1.826

Review 4.  Nucleoside triphosphate-dependent restriction enzymes.

Authors:  D T Dryden; N E Murray; D N Rao
Journal:  Nucleic Acids Res       Date:  2001-09-15       Impact factor: 16.971

5.  Lack of regulation of the modification-dependent restriction enzyme McrBC in Escherichia coli.

Authors:  Mark Murphy; Stefanie Schmid Nuoffer; Thomas A Bickle
Journal:  J Bacteriol       Date:  2002-03       Impact factor: 3.490

6.  Short-range and long-range context effects on coliphage T4 endonuclease II-dependent restriction.

Authors:  K Carlson; L D Kosturko; A C Nyström
Journal:  J Bacteriol       Date:  1996-11       Impact factor: 3.490

7.  Roles of PriA protein and double-strand DNA break repair functions in UV-induced restriction alleviation in Escherichia coli.

Authors:  Ivana Ivancić-Bacće; Ignacija Vlasić; Gordana Cogelja-Cajo; Krunoslav Brcić-Kostić; Erika Salaj-Smic
Journal:  Genetics       Date:  2006-10-08       Impact factor: 4.562

8.  McrBs, a modulator peptide for McrBC activity.

Authors:  D Panne; E A Raleigh; T A Bickle
Journal:  EMBO J       Date:  1998-09-15       Impact factor: 11.598

Review 9.  Diverse functions of restriction-modification systems in addition to cellular defense.

Authors:  Kommireddy Vasu; Valakunja Nagaraja
Journal:  Microbiol Mol Biol Rev       Date:  2013-03       Impact factor: 11.056

10.  Extensive DNA mimicry by the ArdA anti-restriction protein and its role in the spread of antibiotic resistance.

Authors:  Stephen A McMahon; Gareth A Roberts; Kenneth A Johnson; Laurie P Cooper; Huanting Liu; John H White; Lester G Carter; Bansi Sanghvi; Muse Oke; Malcolm D Walkinshaw; Garry W Blakely; James H Naismith; David T F Dryden
Journal:  Nucleic Acids Res       Date:  2009-06-08       Impact factor: 16.971

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