Bmf: A Proapoptotic BH3-Only Protein Regulated by Interaction with the Myosin V Actin Motor Complex, Activated by Anoikis

Author:

Puthalakath Hamsa1,Villunger Andreas1,O'Reilly Lorraine A.1,Beaumont Jennifer G.1,Coultas Leigh1,Cheney Richard E.2,Huang David C. S.1,Strasser Andreas1

Affiliation:

1. The Walter and Eliza Hall Institute of Medical Research, Melbourne, P.O. Royal Melbourne Hospital, 3050 VIC, Australia.

2. University of North Carolina, Chapel Hill, NC 27599–7545, USA

Abstract

Bcl-2 family members bearing only the BH3 domain are essential inducers of apoptosis. We identified a BH3-only protein, Bmf, and show that its BH3 domain is required both for binding to prosurvival Bcl-2 proteins and for triggering apoptosis. In healthy cells, Bmf is sequestered to myosin V motors by association with dynein light chain 2. Certain damage signals, such as loss of cell attachment (anoikis), unleash Bmf, allowing it to translocate and bind prosurvival Bcl-2 proteins. Thus, at least two mammalian BH3-only proteins, Bmf and Bim, function to sense intracellular damage by their localization to distinct cytoskeletal structures.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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