Requirement of poly(ADP-ribose) polymerase in recovery from DNA damage in mice and in cells

被引:860
作者
deMurcia, JM
Niedergang, C
Trucco, C
Ricoul, M
Dutrillaux, B
Mark, M
Oliver, FJ
Masson, M
Dierich, A
LeMeur, M
Walztinger, C
Chambon, P
deMurcia, G
机构
[1] CENFAR,DEPT RADIOBIOL,F-92255 FONTENAY ROSES,FRANCE
[2] UNIV LOUIS PASTEUR STRASBOURG 1,INSERM,CNRS,INST GENET & BIOL MOL CELLULAIRE,COLL FRANCE,F-67404 ILLKIRCH GRAFFENS,FRANCE
关键词
cellular response to DNA damage; gamma-rays; alkylating agents; G(2) arrest; apoptosis);
D O I
10.1073/pnas.94.14.7303
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Poly(ADP-ribose) polymerase [PARP; NAD(+) ADP-ribosyltransferase; NAD(+): poly(adenosine-diphosphate-D-ribosyl)-acceptor ADP-D-ribosyltransferase, EC 2.4.2.30] is a zinc-finger DNA-binding protein that detects specifically DNA strand breaks generated by genotoxic agents. To determine its biological function, me have inactivated both alleles by gene targeting in mice. Treatment of PARP(-/-) mice either by the alkylating agent N-methyl-N-nitrosourea (MNU) or by gamma-irradiation revealed an extreme sensitivity and a high genomic instability to both agents. Following whole body gamma-irradiation (8 Gy) mutant mice died rapidly from acute radiation toxicity to the small intestine. Mice-derived PARP(-/-) cells displayed a high sensitivity to MNU exposure: a G(2)/M arrest in mouse embryonic fibroblasts and a rapid apoptotic response and a p53 accumulation were observed in splenocytes. Altogether these results demonstrate that PARP is a survival factor playing an essential and positive role during DNA damage recovery.
引用
收藏
页码:7303 / 7307
页数:5
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