Published 5 August 2002. doi:10.1083/jcb.200205031
© The Rockefeller University Press,
0021-9525/2002/8/445 $5.00
The Journal of Cell Biology, Volume 158, Number 3, August 5, 2002 445-452
The WD repeat protein, Mdv1p, functions as a molecular adaptor by interacting with Dnm1p and Fis1p during mitochondrial fission
Quinton Tieu,
Voytek Okreglak,
Kari Naylor and
Jodi Nunnari
Section of Molecular and Cellular Biology, University of California, Davis, Davis, CA 95616
Address correspondence to Jodi Nunnari, Section of Molecular and Cellular Biology, University of California, Davis, 3220 Briggs Hall/LSA, Davis, CA 95616-8535. Tel.: (530) 754-9774. Fax: (530) 752-7522. E-mail: jmnunnari{at}ucdavis.edu
Yeast mitochondrial fission is a multistep process during which the dynamin-related GTPase, Dnm1p, assembles into punctate structures that associate with the outer mitochondrial membrane and mediate mitochondrial division. Steps in the Dnm1p-dependent process of fission are regulated by the actions of the WD repeat protein, Mdv1p, and the mitochondrial outer membrane protein, Fis1p. Our previous studies suggested a model where Mdv1p functions to regulate fission at a post-Dnm1p assembly step and Fis1p functions at two distinct steps, at an early point, to regulate Dnm1p assembly, and later, together with Mdv1p, to facilitate Dnm1p-dependent mitochondrial fission. To test this model, we have examined the physical and functional relationship between Mdv1p and Fis1p and present genetic, biochemical, and two-hybrid data indicating that a Fis1pMdv1p complex is required to regulate mitochondrial fission. To further define the role of Mdv1p in fission, we examined the structural features of Mdv1p required for its interactions with Dnm1p and Fis1p. Data from two-hybrid analyses and GFP-tagged domains of Mdv1p indicate that it contains two functionally distinct domains that enable it to function as a molecular adaptor to regulate sequential interactions between Dnm1p and Fis1p and catalyze a rate-limiting step in mitochondrial fission.
Key Words: mitochondria; membranes; fission; dynamin-related GTPase; WD repeat

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