Progressive mitochondrial damage and the resulting dysfunction are key contributors to many human diseases. Eukaryotic cells have a multi-layered system for damage prevention and response. Many studies in humans and a variety of model systems have implicated mitochondrial protein degradation as one of the first lines of defense. We have uncovered a system, centered on the evolutionarily conserved Vms1 protein, that promotes the removal of proteins from the mitochondrial outer membrane in a stress- responsive manner. We propose an ambitious inter-disciplinary plan to describe the regulation and function of this protein and its associates in mitochondrial quality control. First, we propose to define the structural and biochemical basis for the stress-responsive localization of Vms1 to mitochondria. This involves both an inhibitory intramolecular interaction and the interaction of Vms1 with a modified sphingolipid. Second, we propose to determine the mechanisms underlying the stress-responsiveness of Vms1 localization, with an initial focus on a lipid-modifying enzyme that migrates to mitochondria under stress. We will also confirm our preliminary data suggesting that these mechanisms are operative in mammalian cells. Finally, we will determine the biochemical and physiological function of Vms1 in mammals using a combination of cell culture and mouse models. This includes the identification of degradation substrates as well as defining the phenotype of a mouse lacking Vms1.

Public Health Relevance

The progressive deterioration of mitochondrial function has been implicated in a number of chronic diseases. We have uncovered a system employed by the cell to maintain mitochondrial function through the removal of proteins from the mitochondrial outer membrane. We propose to elucidate the details and importance of this system using a combination of structural biology, biochemistry, genetics and cell biology in yeast, mammalian cells and mouse model systems.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM115129-01A1
Application #
8988012
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Anderson, Vernon
Project Start
2015-07-01
Project End
2019-03-31
Budget Start
2015-07-01
Budget End
2016-03-31
Support Year
1
Fiscal Year
2015
Total Cost
Indirect Cost
Name
University of Utah
Department
Biochemistry
Type
Schools of Medicine
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Nowinski, Sara M; Van Vranken, Jonathan G; Dove, Katja K et al. (2018) Impact of Mitochondrial Fatty Acid Synthesis on Mitochondrial Biogenesis. Curr Biol 28:R1212-R1219
Van Vranken, Jonathan G; Nowinski, Sara M; Clowers, Katie J et al. (2018) ACP Acylation Is an Acetyl-CoA-Dependent Modification Required for Electron Transport Chain Assembly. Mol Cell 71:567-580.e4
Nielson, Jason R; Rutter, Jared P (2018) Lipid-mediated signals that regulate mitochondrial biology. J Biol Chem 293:7517-7521
Nielson, Jason R; Fredrickson, Eric K; Waller, T Cameron et al. (2017) Sterol Oxidation Mediates Stress-Responsive Vms1 Translocation to Mitochondria. Mol Cell 68:673-685.e6
Van Vranken, Jonathan G; Rutter, Jared (2016) The Whole (Cell) Is Less Than the Sum of Its Parts. Cell 166:1078-1079