A mitochondrial-focused genetic interaction map reveals a scaffold-like complex required for inner membrane organization in mitochondria

Author:

Hoppins Suzanne1,Collins Sean R.2,Cassidy-Stone Ann1,Hummel Eric3,DeVay Rachel M.1,Lackner Laura L.1,Westermann Benedikt3,Schuldiner Maya4,Weissman Jonathan S.5,Nunnari Jodi1

Affiliation:

1. Department of Molecular and Cellular Biology, University of California, Davis, Davis, CA 95616

2. Department of Chemical and Systems Biology, Stanford University, Stanford, CA 94305

3. Institut für Zellbiologie, Universität Bayreuth, 95440 Bayreuth, Germany

4. Department of Molecular Genetics, Weizmann Institute of Sciences, Rehovot 76100, Israel

5. Department of Cellular and Molecular Pharmacology, Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA 94158

Abstract

To broadly explore mitochondrial structure and function as well as the communication of mitochondria with other cellular pathways, we constructed a quantitative, high-density genetic interaction map (the MITO-MAP) in Saccharomyces cerevisiae. The MITO-MAP provides a comprehensive view of mitochondrial function including insights into the activity of uncharacterized mitochondrial proteins and the functional connection between mitochondria and the ER. The MITO-MAP also reveals a large inner membrane–associated complex, which we term MitOS for mitochondrial organizing structure, comprised of Fcj1/Mitofilin, a conserved inner membrane protein, and five additional components. MitOS physically and functionally interacts with both outer and inner membrane components and localizes to extended structures that wrap around the inner membrane. We show that MitOS acts in concert with ATP synthase dimers to organize the inner membrane and promote normal mitochondrial morphology. We propose that MitOS acts as a conserved mitochondrial skeletal structure that differentiates regions of the inner membrane to establish the normal internal architecture of mitochondria.

Publisher

Rockefeller University Press

Subject

Cell Biology

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