共 77 条
DNA structure dependent checkpoints as regulators of DNA repair
被引:120
作者:

Carr, AM
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Sussex, Genome Damage & Stabil Ctr, Falmer BN1 9RQ, Sussex, England Univ Sussex, Genome Damage & Stabil Ctr, Falmer BN1 9RQ, Sussex, England
机构:
[1] Univ Sussex, Genome Damage & Stabil Ctr, Falmer BN1 9RQ, Sussex, England
来源:
关键词:
SMC;
BRCT-domain;
cell cycle;
recombination;
D O I:
10.1016/S1568-7864(02)00165-9
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Checkpoint proteins were initially identified because their loss of function resulted in defects in cell cycle arrest in response to genotoxic treatments. Initially, the analysis of checkpoint pathways concentrated on their function as signal transducers and how the checkpoint signals were communicated to the core cell cycle machinery and transcriptional apparatus. Although some of the early genetic analysis indicated a complex relationship between DNA replication, DNA repair and the checkpoint pathways, it is only now becoming apparent that checkpoint proteins regulate multiple DNA repair and replication functions. Furthermore, recent data suggest that some checkpoint proteins may participate directly in DNA repair events. In this review I summarise the current models for DNA structure-dependent checkpoint activation and review the evidence linking checkpoint proteins both directly and indirectly to DNA repair. (C) 2002 Elsevier Science B.V. All rights reserved.
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收藏
页码:983 / 994
页数:12
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