Literature DB >> 11106642

Escherichia coli MutS,L modulate RuvAB-dependent branch migration between diverged DNA.

A Fabisiewicz1, L Worth.   

Abstract

This study examines the interaction between Escherichia coli MutS,L and E. coli RuvAB during E. coli RecA-promoted strand exchange. RuvAB is a branch migration complex that stimulates heterologous strand exchange. Previous studies indicate that RuvAB increases the rate at which heteroduplex products are formed by RecA, that RuvA and RuvB are required for this stimulation, and that RuvAB does not stimulate homologous strand exchange. This study indicates that MutS,L inhibit the formation of full-length heteroduplex DNA between M13-fd DNA in the presence of RuvAB, such that less than 2% of the linear substrate is converted to product. Inhibition depends on the time at which MutS,L are added to the reaction and is strongest when MutS,L are added during initiation. The kinetics of the strand exchange reaction suggest that MutS,L directly inhibit RuvAB-dependent branch migration in the absence of RecA. The inhibition requires the formation of base-base mismatches and ATP utilization; no effect on RuvAB-promoted strand exchange is seen if an ATP-deficient mutant of MutS (MutS501) is included in the reaction instead of wild-type MutS. These results are consistent with a role for MutS,L in maintaining genomic stability and replication fidelity.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11106642     DOI: 10.1074/jbc.M005176200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  13 in total

1.  MutS inhibits RecA-mediated strand exchange with platinated DNA substrates.

Authors:  Melissa A Calmann; M G Marinus
Journal:  Proc Natl Acad Sci U S A       Date:  2004-09-16       Impact factor: 11.205

2.  Meiotic recombination between paralogous RBCSB genes on sister chromatids of Arabidopsis thaliana.

Authors:  John G Jelesko; Kristy Carter; Whitney Thompson; Yuki Kinoshita; Wilhelm Gruissem
Journal:  Genetics       Date:  2004-02       Impact factor: 4.562

3.  The frequency and structure of recombinant products is determined by the cellular level of MutL.

Authors:  Marina Elez; Miroslav Radman; Ivan Matic
Journal:  Proc Natl Acad Sci U S A       Date:  2007-05-14       Impact factor: 11.205

4.  Biochemistry of Meiotic Recombination: Formation, Processing, and Resolution of Recombination Intermediates.

Authors:  Kirk T Ehmsen; Wolf-Dietrich Heyer
Journal:  Genome Dyn Stab       Date:  2008-04-05

5.  Genetic exchange between homeologous sequences in mammalian chromosomes is averted by local homology requirements for initiation and resolution of recombination.

Authors:  Derek Yang; Edie B Goldsmith; Yunfu Lin; Barbara Criscuolo Waldman; Vimala Kaza; Alan S Waldman
Journal:  Genetics       Date:  2006-07-02       Impact factor: 4.562

6.  Impact of mutS inactivation on foreign DNA acquisition by natural transformation in Pseudomonas stutzeri.

Authors:  Petra Meier; Wilfried Wackernagel
Journal:  J Bacteriol       Date:  2005-01       Impact factor: 3.490

Review 7.  Targeting and processing of site-specific DNA interstrand crosslinks.

Authors:  Karen M Vasquez
Journal:  Environ Mol Mutagen       Date:  2010-07       Impact factor: 3.216

8.  Distinct roles for the Saccharomyces cerevisiae mismatch repair proteins in heteroduplex rejection, mismatch repair and nonhomologous tail removal.

Authors:  Tamara Goldfarb; Eric Alani
Journal:  Genetics       Date:  2004-10-16       Impact factor: 4.562

9.  Enhanced levels of lambda Red-mediated recombinants in mismatch repair mutants.

Authors:  Nina Costantino; Donald L Court
Journal:  Proc Natl Acad Sci U S A       Date:  2003-12-12       Impact factor: 11.205

10.  DNA Mismatch Repair.

Authors:  M G Marinus
Journal:  EcoSal Plus       Date:  2012-11
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.