The p38-mediated stress-activated checkpoint - A rapid response system for delaying progression through antephase and entry into mitosis

被引:79
作者
Mikhailov, A
Shinohara, M
Rieder, CL
机构
[1] New York State Dept Hlth, Wadsworth Ctr, Lab Cell Regulat, Div Mol Med, Albany, NY 12201 USA
[2] SUNY Albany, Sch Publ Hlth, Dept Biomed Sci, Albany, NY USA
关键词
topoisomerase II; p38; antephase; stress reponse; checkpoint; mitosis;
D O I
10.4161/cc.4.1.1357
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cells have evolved a number of control pathways that delay or prevent them from entering mitosis under conditions that can compromise genome integrity. One recently appreciated and versatile control pathway involves the p38 stress activated protein kinase. During late G(2) p38 is rapidly activated by diverse stresses ( topoisomerase II ( topo II)) and histone deacetylase inhibitors, osmotic shock, microtubule disassembly, UV light, etc) via a number of different pathways. Once activated p38 appears to delay entry into mitosis by inhibiting cdc25B phosphatase that, in turn, down-regulates cyclin A/CDK2 activity. Depending on the agent and degree of stress, this delay may be transient, or it may last until transcription mediated checkpoint pathways can take over.
引用
收藏
页码:57 / 62
页数:6
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