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

被引:0
|
作者
A Dumay
C Laulier
P Bertrand
Y Saintigny
F Lebrun
J-L Vayssière
B S Lopez
机构
[1] UMR 217 CNRS/CEA,
[2] DSV,undefined
[3] DRR,undefined
[4] Fontenay aux RosesCédex,undefined
[5] CNRS-FRE 2445,undefined
[6] Laboratoire de génétique et de biologie cellulaire,undefined
[7] Université Versailles/Saint Quentin-en-Yvelines,undefined
来源
Oncogene | 2006年 / 25卷
关键词
homologous recombination; double-strand break repair; genetic instability; Bcl-2 family; BAX; BID; apoptosis;
D O I
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学科分类号
摘要
In order to analyse the relationships between regulation of apoptosis and homologous recombination (HR), we overexpressed 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 γ-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.
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页码:3196 / 3205
页数:9
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