生物
Bcl-2家族
程序性细胞死亡
细胞生物学
Bcl xL型
蛋白质家族
肽序列
转染
细胞凋亡
细胞培养
遗传学
基因
作者
Jessica M. Boyd,G J Gallo,Elangovan Boobalan,Anne B. Houghton,Scott Malstrom,B J Avery,R. G. Ebb,T. Subramanian,Thomas W. Chittenden,R J Lutz
出处
期刊:PubMed
[National Institutes of Health]
日期:1995-11-02
卷期号:11 (9): 1921-8
被引量:431
摘要
The survival-promoting activity of the Bcl-2 family of proteins appears to be modulated by interactions between various cellular proteins. We have identified a novel cellular protein, Bik, that interacts with the cellular survival-promoting proteins, Bcl-2 and Bcl-xL, as well as the viral survival-promoting proteins, Epstein Barr virus-BHRF1 and adenovirus E1B-19 kDa. In transient transfection assays, Bik promotes cell death in a manner similar to the death-promoting members of the Bcl-2 family, Bax and Bak. This death-promoting activity of Bik can be suppressed by coexpression of Bcl-2, Bcl-XL, EBV-BHRF1 and E1B-19 kDa proteins suggesting that Bik may be a common target for both cellular and viral anti-apoptotic proteins. While Bik does not show overt homology to the BH1 and BH2 conserved domains characteristic of the Bcl-2 family, it does share a 9 amino acid domain (BH3) with Bax and Bak which may be a critical determinant for the death-promoting activity of these proteins.
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