MODULATION OF APOPTOSIS BY THE WIDELY DISTRIBUTED BCL-2 HOMOLOG BAK

被引:478
作者
KIEFER, MC
BRAUER, MJ
POWERS, VC
WU, JJ
UMANSKY, SR
TOMEI, LD
BARR, PJ
机构
[1] LXR Biotechnology Inc., Richmond, CA 94804
关键词
D O I
10.1038/374736a0
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
MEMBERS Of the Bcl-2 family of proteins are characterized by their ability to modulate cell death, Bcl-2 and some of its homologues inhibit apoptosis(1-4), whereas other family members, such as Bax, will accelerate apoptosis under certain conditions(5). Here we describe the identification and characterization of a complementary DNA that encodes a previously unknown Bcl-2 homologue designated Bak. Like Bax, the bak gene product primarily enhances apoptotic cell death following an appropriate stimulus. Unlike Bax, however, Bak can inhibit cell death in an Epstein-Barr-virus-transformed cell line. The widespread tissue distribution of Bak messenger RNA, including those containing long-lived, terminally differentiated cell types, suggests that cell-death-inducing activity is broadly distributed, and that tissue-specific modulation of apoptosis is controlled primarily by regulation of molecules that inhibit apoptosis.
引用
收藏
页码:736 / 739
页数:4
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