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Mitochondrial homeostasis reflects a dynamic balance between membrane fission and fusion events thought essential for mitochondrial function. We report here that altered expression of the C. elegans BCL2 homolog CED-9 affects both mitochondrial fission and fusion. Although striated muscle cells lacking CED-9 have no alteration in mitochondrial size or ultrastructure, these cells appear more sensitive to mitochondrial fragmentation. By contrast, increased CED-9 expression in these cells produces highly interconnected mitochondria. This mitochondrial phenotype is partially suppressed by increased expression of the dynamin-related GTPase DRP-1, with suppression dependent on the BH3 binding pocket of CED-9. This suppression suggests that CED-9 directly regulates DRP-1, a model supported by our finding that CED-9 activates the GTPase activity of human DRP1. Thus, CED-9 is capable of regulating the mitochondrial fission-fusion cycle but is not essential for either fission or fusion.
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JCS ePress
online publication date 30 Sep 2008
doi: 10.1242/jcs.032904
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121/20/3373
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CED-9 and mitochondrial homeostasis in C. elegans muscle
* Author for correspondence (e-mail: hill{at}jhu.edu)
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S. G. Rolland, Y. Lu, C. N. David, and B. Conradt
The BCL-2-like protein CED-9 of C. elegans promotes FZO-1/Mfn1,2- and EAT-3/Opa1-dependent mitochondrial fusion
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S. B. Berman, Y.-b. Chen, B. Qi, J. M. McCaffery, E. B. Rucker III, S. Goebbels, K.-A. Nave, B. A. Arnold, E. A. Jonas, F. J. Pineda, et al.
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© The Company of Biologists Ltd 2008