Abstract
AbstractMitochondrial fission is critically important for controlling mitochondrial morphology, function, quality and transport. Drp1 is the master regulator driving mitochondrial fission, but exactly how Drp1 is regulated remains unclear. Here, we identified Drosophila Clueless and its mammalian orthologue CLUH as key regulators of Drp1. As with loss of drp1, depletion of clueless or CLUH results in mitochondrial elongation, while as with drp1 overexpression, clueless or CLUH overexpression leads to mitochondrial fragmentation. Importantly, drp1 overexpression rescues adult lethality, tissue disintegration and mitochondrial defects of clueless null mutants in Drosophila. Mechanistically, Clueless and CLUH promote recruitment of Drp1 to mitochondria from the cytosol. This involves CLUH binding to mRNAs encoding Drp1 receptors MiD49 and Mff, and regulation of their translation. Our findings identify a crucial role of Clueless and CLUH in controlling mitochondrial fission through regulation of Drp1.
Funder
China Scholarship Council
UCLA Dissertation Year Fellowship
The Wellcome Trust-NIH PhD Studentship
Glenn Foundation for Medical Research
U.S. Department of Health & Human Services | NIH | National Institute on Aging
National Institute on Aging, Kenneth Glenn Family Foundation, Louis B. Mayer Foundation, UCLA Laurie and Steven Gordon Commitment to Cure Parkinson’s Disease, Renee and Meyer Luskin Family Fund
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary
Cited by
27 articles.
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