Overall Cdk activity modulates the DNA damage response in mammalian cells

被引:49
作者
Cerqueira, Antonio [1 ]
Santamaria, David [1 ]
Martinez-Pastor, Barbara [2 ]
Cuadrado, Miriam [2 ]
Fernandez-Capetillo, Oscar [2 ]
Barbacid, Mariano [1 ]
机构
[1] Ctr Nacl Invest Oncol, Mol Oncol Programme, Expt Oncol Grp, E-28029 Madrid, Spain
[2] Ctr Nacl Invest Oncol, Mol Oncol Programme, Genom Instabil Grp, E-28029 Madrid, Spain
基金
欧洲研究理事会;
关键词
DOUBLE-STRAND BREAKS; CYCLIN-DEPENDENT KINASES; END RESECTION; HOMOLOGOUS RECOMBINATION; CHECKPOINT RESPONSE; IN-VIVO; S-PHASE; ATM; PHOSPHORYLATION; REPAIR;
D O I
10.1083/jcb.200903033
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In response to DNA damage, cells activate a phosphorylation-based signaling cascade known as the DNA damage response (DDR). One of the main outcomes of DDR activation is inhibition of cyclin-dependent kinase (Cdk) activity to restrain cell cycle progression until lesions are healed. Recent studies have revealed a reverse connection by which Cdk activity modulates processing of DNA break ends and DDR activation. However, the specific contribution of individual Cdks to this process remains poorly understood. To address this issue, we have examined the DDR in murine cells carrying a defined set of Cdks. Our results reveal that genome maintenance programs of post-replicative cells, including DDR, are regulated by the overall level of Cdk activity and not by specific Cdks.
引用
收藏
页码:773 / 780
页数:8
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