Apoptosis-stimulating protein of p53-2 (ASPP2/53BP2L) is an E2F target gene

被引:54
作者
Chen, D
Padiernos, E
Ding, F
Lossos, IS
Lopez, CD
机构
[1] Oregon Hlth & Sci Univ, Dept Med, Div Hematol & Med Oncol, Portland, OR 97239 USA
[2] Univ Miami, Sylvester Comprehens Canc Ctr, Dept Med, Div Hematol Oncol, Miami, FL 33136 USA
[3] Univ Miami, Dept Mol & Cellular Pharmacol, Miami, FL 33136 USA
关键词
ASPP2; 53BP2; p53; E2F; apoptosis;
D O I
10.1038/sj.cdd.4401536
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 p53 pathway is a central apoptotic regulator. Deregulation of the Rb/E2F pathway occurs in a majority of tumors, resulting in both unrestrained proliferation and enhanced apoptosis sensitivity via p53-dependent and independent mechanisms. However, the mechanisms coupling the p53 and Rb/E2F pathways remain incompletely understood. We report that ASPP2/(53BP2L), a p53/p73-binding protein that promotes p53/p73-dependent apoptosis, is an E2F target gene. The ASPP2/53BP2L promoter was identified and ectopic expression of transcription-competent E2F-1 (E2F-2 and E2F-3) stimulated an ASPP2/(53BP2L) promoter-luciferase reporter. Mutational analysis of the ASPP2/(53BP2L) promoter identified E2F-binding sites that cooperate for E2F-1 induction and basal repression of ASPP2/(53BP2L). Moreover, endogenous ASPP2/(53BP2L) levels increased after E2F-1 expression, and E2F-1 bound the endogenous ASPP2/(53BP2L) promoter after chromatin immunoprecipitation. Typical for an E2F target, ASPP2/(53BP2L) expression was maximal in early S-phase. Thus, ASPP2/(53BP2L) is downstream of E2F, suggesting that it functions as a common link between the p53/p73 and Rb/E2F apoptotic pathways.
引用
收藏
页码:358 / 368
页数:11
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