YAMA/CPP32-BETA, A MAMMALIAN HOMOLOG OF CED-3, IS A CRMA-INHIBITABLE PROTEASE THAT CLEAVES THE DEATH SUBSTRATE POLY(ADP-RIBOSE) POLYMERASE

被引:2356
作者
TEWARI, M
QUAN, LT
OROURKE, K
DESNOYERS, S
ZENG, Z
BEIDLER, DR
POIRIER, GG
SALVESEN, GS
DIXIT, VM
机构
[1] UNIV MICHIGAN,SCH MED,GRAD PROGRAM CELLULAR & MOLEC BIOL,ANN ARBOR,MI 48109
[2] DUKE UNIV,MED CTR,DEPT PATHOL,DURHAM,NC 27710
[3] CHU LAVAL,RES CTR,MOLEC ENDOCRINOL LAB,POLY ADPRIBOSE METAB GRP,ST FOY,PQ G1V 4G2,CANADA
[4] UNIV LAVAL,ST FOY,PQ G1V 4G2,CANADA
关键词
D O I
10.1016/0092-8674(95)90541-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Although the mechanism of mammalian apoptosis has not been elucidated, a protease of the CED-3/ICE family is anticipated to be a component of the death machinery. Several lines of evidence predict that this protease cleaves the death substrate poly(ADP-ribose) polymerase (PARP) to a specific 85 kDa form observed during apoptosis, is inhibitable by the CrmA protein, and is distinct from ICE, We cloned a ced-3/ICE-related gene, designated Yama, that encodes a protein identical to CPP32 beta. Purified Yama was a zymogen that, when activated, cleaved PARP to generate the 85 kDa apoptotic fragment. Cleavage of PARP by Yama was inhibited by CrmA but not by an inactive point mutant of CrmA. Furthermore, CrmA blocked cleavage of PARP in cells undergoing apoptosis. We propose that Yama may represent an effector component of the mammalian cell death pathway and suggest that CrmA blocks apoptosis by inhibiting Yama.
引用
收藏
页码:801 / 809
页数:9
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