Replication Stress-Induced Genome Instability: The Dark Side of Replication Maintenance by Homologous Recombination

被引:136
作者
Carr, Antony M. [1 ]
Lambert, Sarah [2 ,3 ]
机构
[1] Univ Sussex, Genome Damage & Stabil Ctr, Sch Life Sci, Brighton BN1 9RQ, E Sussex, England
[2] Inst Curie, F-91405 Orsay, France
[3] Univ Paris 11, Ctr Univ, Ctr Natl Rech Sci, UMR 3348, F-91405 Orsay, France
基金
英国医学研究理事会;
关键词
homologous recombination; DNA replication; genome instability; genomic disorders; INDUCED DNA-DAMAGE; BREAK-INDUCED REPLICATION; COMMON FRAGILE SITES; INVERTED REPEATS; FORK PROGRESSION; DORMANT ORIGINS; EXCESS MCM2-7; REPAIR; REARRANGEMENTS; COMPLEX;
D O I
10.1016/j.jmb.2013.04.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Homologous recombination (HR) is an evolutionary-conserved mechanism involved in a subtle balance between genome stability and diversity. HR is a faithful DNA repair pathway and has been largely characterized in the context of double-strand break (DSB) repair. Recently, multiple functions for the HR machinery have been identified at arrested forks. These are evident across different organisms and include replication fork-stabilization and fork-restart functions. Interestingly, a DSB appears not to be a prerequisite for HR-mediated replication maintenance. HR has the ability to rebuild a replisome at inactivated forks, but perhaps surprisingly, the resulting replisome is liable to intrastrand and interstrand switches leading to replication errors. Here, we review our current understanding of the replication maintenance function of HR. The error proneness of these pathways leads us to suggest that the origin of replication-associated genome instability should be re-evaluated. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4733 / 4744
页数:12
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