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Bmf: A Proapoptotic BH3-Only Protein Regulated by Interaction with the Myosin V Actin Motor Complex, Activated by Anoikis
661
Citations
21
References
2001
Year
Molecular RegulationApoptosisMolecular BiologyCell DeathCytoskeletonBh3-only ProteinCellular PhysiologySignaling PathwayCell RegulationProapoptotic Bh3-only ProteinBcl-2 Family MembersCell SignalingProtein FunctionMolecular PhysiologyBh3 DomainCell BiologyProtein PhosphorylationSignal TransductionNatural SciencesCell MotilityCellular BiochemistrySystems BiologyMedicine
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.
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