Localization of checkpoint and repair proteins in eukaryotes

被引:50
作者
Lisby, M
Rothstein, R
机构
[1] Columbia Univ Coll Phys & Surg, Dept Genet & Dev, New York, NY 10032 USA
[2] Univ Copenhagen, Inst Mol Biol, DK-1353 Copenhagen, Denmark
关键词
double-strand break; replication; DNA damage; checkpoint; foci; homologous recombination; non-homologous end-joining; repair center;
D O I
10.1016/j.biochi.2004.10.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In eukaryotes, the cellular response to DNA damage depends on the type of DNA structure being recognized by the checkpoint and repair machinery. DNA ends and single-stranded DNA are hallmarks of double-strand breaks and replication stress. These two structures are recognized by distinct sets of proteins, which are reorganized into a focal assembly at the lesion. Moreover, the composition of these foci is coordinated with cell cycle progression, reflecting the favoring of end-joining in the G1 phase and homologous recombination in S and G2. The assembly of proteins at sites of DNA damage is largely controlled by a network of protein-protein interactions, with the Mre11 complex initiating assembly at DNA ends and replication protein A directing recruitment to single-stranded DNA. This review summarizes current knowledge on the cellular organization of DSB repair and checkpoint proteins focusing on budding yeast and mammalian cells. (C) 2004 Elsevier SAS. All rights reserved.
引用
收藏
页码:579 / 589
页数:11
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