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Dev Cell. 2014 Jan 27;28(2):161-73. doi: 10.1016/j.devcel.2013.12.009. Epub 2014 Jan 16.

Stress-induced nuclear-to-cytoplasmic translocation of cyclin C promotes mitochondrial fission in yeast.

Author information

1
Department of Molecular Biology, Rowan University School of Osteopathic Medicine, Stratford, NJ 08084, USA.
2
Department of Molecular Biology, Rowan University School of Osteopathic Medicine, Stratford, NJ 08084, USA. Electronic address: strichra@rowan.edu.

Abstract

Mitochondrial morphology is maintained by the opposing activities of dynamin-based fission and fusion machines. In response to stress, this balance is dramatically shifted toward fission. This study reveals that the yeast transcriptional repressor cyclin C is both necessary and sufficient for stress-induced hyperfission. In response to oxidative stress, cyclin C translocates from the nucleus to the cytoplasm, where it is destroyed. Prior to its destruction, cyclin C both genetically and physically interacts with Mdv1p, an adaptor that links the GTPase Dnm1p to the mitochondrial receptor Fis1p. Cyclin C is required for stress-induced Mdv1p mitochondrial recruitment and the efficient formation of functional Dnm1p filaments. Finally, coimmunoprecipitation studies and fluorescence microscopy revealed an elevated association between Mdv1p and Dnm1p in stressed cells that is dependent on cyclin C. This study provides a mechanism by which stress-induced gene induction and mitochondrial fission are coordinated through translocation of cyclin C.

PMID:
24439911
PMCID:
PMC3963397
DOI:
10.1016/j.devcel.2013.12.009
[Indexed for MEDLINE]
Free PMC Article

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