Eplication licensing and the DNA damage checkpoint

被引:23
作者
Cook, Jeanette Gowen [1 ,2 ]
机构
[1] Univ N Carolina, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Lineberger Comprehens Canc Ctr, Dept Pharmacol, Chapel Hill, NC 27599 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2009年 / 14卷
基金
美国国家卫生研究院;
关键词
DNA replication; licensing; rereplication; preRC; checkpoint; Cdt1; Cdc6; Chk1; ATR; DNA Damage; Cyclin Dependent Kinase; Review; MINICHROMOSOME MAINTENANCE PROTEINS; ORIGIN RECOGNITION COMPLEX; CELL-CYCLE; S-PHASE; UBIQUITIN LIGASE; RE-REPLICATION; MCM PROTEINS; DEPENDENT PHOSPHORYLATION; SACCHAROMYCES-CEREVISIAE; PREVENTS REREPLICATION;
D O I
10.2741/3584
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
Accurate and timely duplication of chromosomal DNA requires that replication be coordinated with processes that ensure genome integrity. Significant advances in determining how the earliest steps in DNA replication are affected by DNA damage have highlighted some of the mechanisms to establish that coordination. Recent insights have expanded the relationship between the ATM and ATR-dependent checkpoint pathways and the proteins that bind and function at replication origins. These findings suggest that checkpoints and replication are more intimately associated than previously appreciated, even in the absence of exogenous DNA damage. This review summarizes some of these developments.
引用
收藏
页码:5013 / 5030
页数:18
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