O'Connor L, Strasser A, O'Reilly L A, Hausmann G, Adams J M, Cory S, Huang D C
The Walter and Eliza Hall Institute of Medical Research, PO Royal Melbourne Hospital, Victoria, Australia.
EMBO J. 1998 Jan 15;17(2):384-95. doi: 10.1093/emboj/17.2.384.
Certain members of the Bcl-2 family inhibit apoptosis while others facilitate this physiological process of cell death. An expression screen for proteins that bind to Bcl-2 yielded a small novel protein, denoted Bim, whose only similarity to any known protein is the short (nine amino acid) BH3 motif shared by most Bcl-2 homologues. Bim provokes apoptosis, and the BH3 region is required for Bcl-2 binding and for most of its cytotoxicity. Like Bcl-2, Bim possesses a hydrophobic C-terminus and localizes to intracytoplasmic membranes. Three Bim isoforms, probably generated by alternative splicing, all induce apoptosis, the shortest being the most potent. Wild-type Bcl-2 associates with Bim in vivo and modulates its death function, whereas Bcl-2 mutants that lack survival function do neither. Significantly, Bcl-xL and Bcl-w, the two closest homologues of Bcl-2, also bind to Bim and inhibit its activity, but more distant viral homologues, adenovirus E1B19K and Epstein-Barr virus BHRF-1, can do neither. Hence, Bim appears to act as a 'death ligand' which can only neutralize certain members of the pro-survival Bcl-2 sub-family.
Bcl-2家族的某些成员可抑制细胞凋亡,而其他成员则促进这种细胞死亡的生理过程。一项针对与Bcl-2结合的蛋白质的表达筛选,产生了一种新的小蛋白质,命名为Bim,它与任何已知蛋白质的唯一相似之处是大多数Bcl-2同源物共有的短(九个氨基酸)BH3基序。Bim可引发细胞凋亡,并且BH3区域对于Bcl-2结合及其大部分细胞毒性是必需的。与Bcl-2一样,Bim具有疏水的C末端,并定位于胞质内膜。三种可能由可变剪接产生的Bim异构体均能诱导细胞凋亡,其中最短的异构体活性最强。野生型Bcl-2在体内与Bim结合并调节其死亡功能,而缺乏生存功能的Bcl-2突变体则不能。值得注意的是,Bcl-2的两个最接近的同源物Bcl-xL和Bcl-w也与Bim结合并抑制其活性,但更远的病毒同源物腺病毒E1B19K和爱泼斯坦-巴尔病毒BHRF-1则不能。因此,Bim似乎作为一种“死亡配体”,只能中和促生存Bcl-2亚家族的某些成员。