Bax and Bid, two proapoptotic Bcl-2 family members, inhibit homologous recombination, independently of apoptosis regulation

被引:35
作者
Dumay, A.
Laulier, C.
Bertrand, P.
Saintigny, Y.
Lebrun, F.
Vayssiére, J-L
Lopez, B. S.
机构
[1] CEA, CNRS, UMR 217, DSV,DRR, F-92265 Fontenay Aux Roses, France
[2] Univ Versailles, Lab Genet & Biol Cellulaire, CNRS, FRE 2445, F-78000 Versailles, France
关键词
homologous recombination; double-strand break repair; genetic instability; Bcl-2; family; BAX; BID; apoptosis;
D O I
10.1038/sj.onc.1209344
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
In order to analyse the relationships between regulation of apoptosis and homologous recombination (HR), we over-expressed proapoptotic Bax or only-BH3 Bid proteins or antiapoptotic Bcl-2 or Bcl-XL, in hamster CHO cells or in SV40-transformed human fibroblasts. We measured HR induced by gamma-rays, UVC or a specific double-strand cleavage targeted in the recombination substrate by the meganuclease I-SceI. We show here that the induction of both recombinant cells and recombinant colonies was impaired when expressing Bcl-2 family members, in hamster as well as in human cells. Moreover, the pro- as well as antiapoptotic Bcl-2 family members inhibited HR, independently of degradation of the RAD51 recombination protein and of their impact on apoptosis. These data reveal a mechanism of HR downregulation by potentially proapoptotic proteins, distinct from and parallel to degradation of recombination proteins, a situation that should also optimize the efficiency of programmed cell death.
引用
收藏
页码:3196 / 3205
页数:10
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