Literature DB >> 15467360

Mismatch repair proteins: key regulators of genetic recombination.

J A Surtees1, J L Argueso, E Alani.   

Abstract

Mismatch repair (MMR) systems are central to maintaining genome stability in prokaryotes and eukaryotes. MMR proteins play a fundamental role in avoiding mutations, primarily by removing misincorporation errors that occur during DNA replication. MMR proteins also act during genetic recombination in steps that include repairing mismatches in heteroduplex DNA, modulating meiotic crossover control, removing 3' non-homologous tails during double-strand break repair, and preventing recombination between divergent sequences. In this review we will, first, discuss roles for MMR proteins in repairing mismatches that occur during recombination, particularly during meiosis. We will also explore how studying this process has helped to refine models of double-strand break repair, and particularly to our understanding of gene conversion gradients. Second, we will examine the role of MMR proteins in repressing homeologous recombination, i.e. recombination between divergent sequences. We will also compare the requirements for MMR proteins in preventing homeologous recombination to the requirements for these proteins in mismatch repair. Copyright 2004 S. Karger AG, Basel.

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Year:  2004        PMID: 15467360     DOI: 10.1159/000080593

Source DB:  PubMed          Journal:  Cytogenet Genome Res        ISSN: 1424-8581            Impact factor:   1.636


  69 in total

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2.  A two-pathway analysis of meiotic crossing over and gene conversion in Saccharomyces cerevisiae.

Authors:  Franklin W Stahl; Henriette M Foss
Journal:  Genetics       Date:  2010-08-02       Impact factor: 4.562

3.  Assessment of anti-recombination and double-strand break-induced gene conversion in human cells by a chromosomal reporter.

Authors:  Keqian Xu; Xiling Wu; Joshua D Tompkins; Chengtao Her
Journal:  J Biol Chem       Date:  2012-07-07       Impact factor: 5.157

4.  Trans events associated with crossovers are revealed in the absence of mismatch repair genes in Saccharomyces cerevisiae.

Authors:  Eva R Hoffmann; Rhona H Borts
Journal:  Genetics       Date:  2005-01-16       Impact factor: 4.562

5.  Saccharomyces cerevisiae MSH2-MSH3 and MSH2-MSH6 complexes display distinct requirements for DNA binding domain I in mismatch recognition.

Authors:  Susan D Lee; Jennifer A Surtees; Eric Alani
Journal:  J Mol Biol       Date:  2006-11-03       Impact factor: 5.469

Review 6.  Mechanisms of RecQ helicases in pathways of DNA metabolism and maintenance of genomic stability.

Authors:  Sudha Sharma; Kevin M Doherty; Robert M Brosh
Journal:  Biochem J       Date:  2006-09-15       Impact factor: 3.857

7.  Bi-directional routing of DNA mismatch repair protein human exonuclease 1 to replication foci and DNA double strand breaks.

Authors:  Sascha E Liberti; Sofie D Andersen; Jing Wang; Alfred May; Simona Miron; Mylene Perderiset; Guido Keijzers; Finn C Nielsen; Jean-Baptiste Charbonnier; Vilhelm A Bohr; Lene J Rasmussen
Journal:  DNA Repair (Amst)       Date:  2010-10-20

8.  Sequence divergence impedes crossover more than noncrossover events during mitotic gap repair in yeast.

Authors:  Caroline Welz-Voegele; Sue Jinks-Robertson
Journal:  Genetics       Date:  2008-06-18       Impact factor: 4.562

9.  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

10.  Distinct requirements within the Msh3 nucleotide binding pocket for mismatch and double-strand break repair.

Authors:  Charanya Kumar; Gregory M Williams; Brett Havens; Michelle K Dinicola; Jennifer A Surtees
Journal:  J Mol Biol       Date:  2013-02-28       Impact factor: 5.469

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