DAP kinase activates a p19ARF/p53-mediated apoptotic checkpoint to suppress oncogenic transformation

被引:308
作者
Raveh, T
Droguett, G
Horwitz, MS
DePinho, RA
Kimchi, A
机构
[1] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
[2] Albert Einstein Coll Med, Dept Microbiol & Immunol, Bronx, NY 10461 USA
[3] Harvard Univ, Sch Med, Dept Med Genet, Boston, MA 02115 USA
[4] Dana Farber Canc Inst, Dep Adult Oncol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/35050500
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
DAP kinase is a pro-apoptotic calcium-regulated serine/threonine kinase, whose expression is frequently lost in human tumours, Here we show that DAP kinase counteracts oncogene-induced transformation by activating a p19(ARF)/p53-dependent apoptotic checkpoint. Ectopic expression of DAP kinase suppressed oncogenic transformation of primary embryonic fibroblasts by activating p53 in a p19(ARF)-dependent manner. Consequently, the fibroblasts underwent apoptosis, characterized by caspase activation and DNA fragmentation. In response to c-Myc or E2F-1, the endogenous DAP kinase protein was upregulated. Furthermore, functional or genetic inactivation of the endogenous DAP kinase reduced the extent of induction of p19(ARF)/p53 and weakened the subsequent apoptotic responses to c-Myc or E2F-1. These results establish a role for DAP kinase in an early apoptotic checkpoint designed to eliminate pre-malignant cells during cancer development.
引用
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页码:1 / 7
页数:7
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