Involvement of the MKK6-p38γ cascade in γ-radiation-induced cell cycle arrest

被引:226
作者
Wang, XF
McGowan, CH
Zhao, M
He, LS
Downey, JS
Fearns, C
Wang, YB
Huang, S
Han, JH
机构
[1] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
[3] Burnham Inst, Program Oncogenes & Tumor Suppressor Genes, La Jolla, CA 92037 USA
[4] Univ Maryland, Sch Med, Dept Physiol, Baltimore, MD 21201 USA
关键词
D O I
10.1128/MCB.20.13.4543-4552.2000
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
The p38 group of kinases belongs to the mitogen-activated protein (MAP) kinase superfamily with structural and functional characteristics distinguishable from those of the ERK, JNK (SAPK), and BMK (ERK5) kinases. Although there is a high degree of similarity among members of the p38 group in terms of structure and activation, each member appears to have a unique function. Here we show that activation of p38 gamma (also known as ERK6 or SAPK3), but not the other p38 isoforms, is required for gamma-irradiation-induced G(2) arrest. Activation of the MKK6-p38 gamma cascade is sufficient to induce G(2) arrest in cells, and expression of dominant negative alleles of MKK6 or p38 gamma allows cells to escape the DNA damage-induce G(2) delay. Activation of p38 gamma is dependent on ATM and leads to activation of Cds1 (also known as Chk2). These data suggest a model in which activation of ATM by gamma irradiation leads to the activation of MKK6, p38 gamma, and Cds1 and that activation of both MKK6 and p38 gamma is essential for the proper regulation of the G(2) checkpoint in mammalian cells.
引用
收藏
页码:4543 / 4552
页数:10
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