Surviving the breakup: The DNA damage checkpoint

被引:420
作者
Harrison, Jacob C. [1 ]
Haber, James E.
机构
[1] Brandeis Univ, Dept Biol, Waltham, MA 02445 USA
[2] Brandeis Univ, Rosenstiel Basic Med Sci Res Ctr, Waltham, MA 02445 USA
关键词
DNA damage checkpoint; double-strand break; Mec1; Rad53; adaptation; recovery;
D O I
10.1146/annurev.genet.40.051206.105231
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In response to even a single chromosomal double-strand DNA break, cells enact the DNA damage checkpoint. This checkpoint triggers cell cycle arrest, providing time for the cell to repair damaged chromosomes before entering mitosis. This mechanism helps prevent the segregation of damaged or mutated chromosomes and thus promotes genomic stability Recent work has elucidated the molecular mechanisms underlying several critical steps in checkpoint activation, notablv the recruitment of the upstream checkpoint kinases of the ATM and ATR families to different damaged DNA structures and the molecular events through which these kinases activate their effectors. Chromatin modification has emerged as one important component of checkpoint activation and maintenance. Following DNA repair, the checkpoint pathway is inactivated in a process termed recovery. A related but genetic-ally distinct process, adaptation, controls cell cycle re-entry in the face of unrepairable damage.
引用
收藏
页码:209 / 235
页数:27
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