Mismatch repair proteins: key regulators of genetic recombination

被引:121
作者
Surtees, JA [1 ]
Argueso, JL [1 ]
Alani, E [1 ]
机构
[1] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
关键词
D O I
10.1159/000080593
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:146 / 159
页数:14
相关论文
共 146 条
[1]   Genetic analysis of mouse embryonic stem cells bearing Msh3 and Msh2 single and compound mutations [J].
Abuin, A ;
Zhang, HJ ;
Bradley, A .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (01) :149-157
[2]   The coordinated functions of the E-coli MutS and MutL proteins in mismatch repair [J].
Acharya, S ;
Foster, PL ;
Brooks, P ;
Fishel, R .
MOLECULAR CELL, 2003, 12 (01) :233-246
[3]  
ALANI E, 1994, GENETICS, V137, P19
[4]   Crystal structure and biochemical analysis of the MutS•ADP•Beryllium fluoride complex suggests a conserved mechanism for ATP interactions in mismatch repair [J].
Alani, E ;
Lee, JY ;
Schofield, MJ ;
Kijas, AW ;
Hsieh, P ;
Yang, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (18) :16088-16094
[5]  
Alani E, 1996, MOL CELL BIOL, V16, P5604
[6]   MutS mediates heteroduplex loop formation by a translocation mechanism [J].
Allen, DJ ;
Makhov, A ;
Grilley, M ;
Taylor, J ;
Thresher, R ;
Modrich, P ;
Griffith, JD .
EMBO JOURNAL, 1997, 16 (14) :4467-4476
[7]   Differential timing and control of noncrossover and crossover recombination during meiosis [J].
Allers, T ;
Lichten, M .
CELL, 2001, 106 (01) :47-57
[8]   Intermediates of yeast meiotic recombination contain heteroduplex DNA [J].
Allers, T ;
Lichten, M .
MOLECULAR CELL, 2001, 8 (01) :225-231
[9]   exo1-Dependent mutator mutations:: Model system for studying functional interactions in mismatch repair [J].
Amin, NS ;
Nguyen, MN ;
Oh, S ;
Kolodner, RD .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (15) :5142-5155
[10]   Systematic mutagenesis of the Saccharomyces cerevisiae MLH1 gene reveals distinct roles for Mlh1p in meiotic crossing over and in vegetative and meiotic mismatch repair [J].
Argueso, JL ;
Kijas, AW ;
Sarin, S ;
Heck, J ;
Waase, M ;
Alani, E .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (03) :873-886