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Fis1, Mff, MiD49, and MiD51 mediate Drp1 recruitment in mitochondrial fission

Molecular Biology of the Cell · 2013 · Vol. 24(5) · pp. 659–667
Oliver C. LosónZhiyin SongHsiuchen ChenDavid C. Chan

Abstract

Several mitochondrial outer membrane proteins-mitochondrial fission protein 1 (Fis1), mitochondrial fission factor (Mff), mitochondrial dynamics proteins of 49 and 51 kDa (MiD49 and MiD51, respectively)-have been proposed to promote mitochondrial fission by recruiting the GTPase dynamin-related protein 1 (Drp1), but fundamental issues remain concerning their function. A recent study supported such a role for Mff but not for Fis1. In addition, it is unclear whether MiD49 and MiD51 activate or inhibit fission, because their overexpression causes extensive mitochondrial elongation. It is also unknown whether these proteins can act in the absence of one another to mediate fission. Using Fis1-null, Mff-null, and Fis1/Mff-null cells, we show that both Fis1 and Mff have roles in mitochondrial fission. Moreover, immunofluorescence analysis of Drp1 suggests that Fis1 and Mff are important for the number and size of Drp1 puncta on mitochondria. Finally, we find that either MiD49 or MiD51 can mediate Drp1 recruitment and mitochondrial fission in the absence of Fis1 and Mff. These results demonstrate that multiple receptors can recruit Drp1 to mediate mitochondrial fission.

Mitochondrial Function and PathologyATP Synthase and ATPases ResearchMetabolism and Genetic DisordersFIS1Mitochondrial fissionBiologyCell biologyFissionMitochondrionGTPasemitochondrial fusionDNAJA3Biochemistry

MeSH terms

AnimalsFibroblastsHeLa CellsHumansMembrane ProteinsMicrotubule-Associated ProteinsPeptide Elongation FactorsMitochondrial ProteinsDynaminsRNA, Small InterferingMitochondrial MembranesMiceMitochondrial Dynamics

Funding

  • National Institutes of Health
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