1. Academic Validation
  2. Bim: a novel member of the Bcl-2 family that promotes apoptosis

Bim: a novel member of the Bcl-2 family that promotes apoptosis

  • EMBO J. 1998 Jan 15;17(2):384-95. doi: 10.1093/emboj/17.2.384.
L O'Connor 1 A Strasser L A O'Reilly G Hausmann J M Adams S Cory D C Huang
Affiliations

Affiliation

  • 1 The Walter and Eliza Hall Institute of Medical Research, PO Royal Melbourne Hospital, Victoria, Australia.
Abstract

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.

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