Bcl-2 mutants with restricted subcellular location reveal spatially distinct pathways for apoptosis in different cell types

被引:284
作者
Zhu, WJ
Cowie, A
Wasfy, GW
Penn, LZ
Leber, B
Andrews, DW
机构
[1] MCMASTER UNIV,DEPT BIOCHEM,HAMILTON,ON L8N 3Z5,CANADA
[2] MCMASTER UNIV,DEPT MED,HAMILTON,ON L8N 3Z5,CANADA
[3] UNIV TORONTO,ONTARIO CANC INST,DEPT MICROBIOL,TORONTO,ON M5G 2C1,CANADA
[4] UNIV TORONTO,ONTARIO CANC INST,DEPT MED BIOPHYS,TORONTO,ON M5G 2C1,CANADA
关键词
apoptosis; bcl-2; insertion sequence; mitochondria; protein targeting;
D O I
10.1002/j.1460-2075.1996.tb00788.x
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
Human Bcl-2 is located in multiple intracellular membranes when expressed in MDCK and Rat-1/myc cells. We restricted expression to the endoplasmic reticulum or mitochondria by exchanging the Bcl-2 carboxyterminal insertion sequence for an equivalent sequence from cytochrome b5 or ActA, respectively MDCK cells are protected from serum deprivation-induced apoptosis by both wild-type Bcl-2 and the mutant targeted to mitochondria but not by the mutant targeted to endoplasmic reticulum. In contrast, when expressed in Rat-1/myc cells, the Bcl-2 mutant located at the endoplasmic reticulum is more effective than that targeted to mitochondria, In MDCK cells both mutants bind Bax as effectively as wild-type, demonstrating that Bax binding is not sufficient to prevent apoptosis.
引用
收藏
页码:4130 / 4141
页数:12
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