New insights into the mechanism of DNA mismatch repair

被引:0
作者
Gloria X. Reyes
Tobias T. Schmidt
Richard D. Kolodner
Hans Hombauer
机构
[1] German Cancer Research Center (DKFZ),Ludwig Institute for Cancer Research, Department of Cellular and Molecular Medicine, Moores
[2] University of California,UCSD Cancer Center and Institute of Genomic Medicine
[3] San Diego School of Medicine,undefined
来源
Chromosoma | 2015年 / 124卷
关键词
Proliferate Cell Nuclear Antigen; Lynch Syndrome; PWWP Domain; MutL Homolog; Mispaired Base;
D O I
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中图分类号
学科分类号
摘要
The genome of all organisms is constantly being challenged by endogenous and exogenous sources of DNA damage. Errors like base:base mismatches or small insertions and deletions, primarily introduced by DNA polymerases during DNA replication are repaired by an evolutionary conserved DNA mismatch repair (MMR) system. The MMR system, together with the DNA replication machinery, promote repair by an excision and resynthesis mechanism during or after DNA replication, increasing replication fidelity by up-to-three orders of magnitude. Consequently, inactivation of MMR genes results in elevated mutation rates that can lead to increased cancer susceptibility in humans. In this review, we summarize our current understanding of MMR with a focus on the different MMR protein complexes, their function and structure. We also discuss how recent findings have provided new insights in the spatio-temporal regulation and mechanism of MMR.
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页码:443 / 462
页数:19
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共 870 条
[1]  
Acharya S(1996)hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6 Proc Natl Acad Sci U S A 93 13629-13634
[2]  
Wilson T(2003)The coordinated functions of the Mol Cell 12 233-246
[3]  
Gradia S(2006) MutS and MutL proteins in mismatch repair Nucleic Acids Res 34 3169-3180
[4]  
Kane MF(1997)Identifying an interaction site between MutH and the C-terminal domain of MutL by crosslinking, affinity purification, chemical coding and mass spectrometry EMBO J 16 4467-4476
[5]  
Guerrette S(2014)MutS mediates heteroduplex loop formation by a translocation mechanism Mol Cell Biol 34 1521-1534
[6]  
Marsischky GT(2001)A Mol Cell Biol 21 5142-5155
[7]  
Kolodner R(2003) RNase H2 interaction network functions to suppress genome instability Biochemistry 42 7682-7693
[8]  
Fishel R(2010)exo1-Dependent mutator mutations: model system for studying functional interactions in mismatch repair DNA Repair (Amst) 9 448-457
[9]  
Acharya S(2014)Mismatch recognition-coupled stabilization of Msh2-Msh6 in an ATP-bound state at the initiation of DNA repair Front Genet 5 287-552
[10]  
Foster PL(1998)Functional residues on the surface of the N-terminal domain of yeast Pms1 Cell 95 541-97