): Mitochondria are remarkably dynamic organelles; they undergo cycles of fusion and fission, in some cases in response to developmental signals. The mitochondrial fusion process is unique among intracellular membrane fusion events, because each organelle contains two sets of lipid bilayers. Recent studies in yeast and flies have identified Fzo, a transmembrane GTPase localized to niitochondria, as an essential molecule in mitochondrial fusion. Moreover, these studies indicate that mitochondrial fusion is essential for normal respiratory function. Intriguingly, Fzo contains several coiled-coil motifs, reminiscent of viral envelope proteins and SNARE complexes that are directly involved in other types of membrane fusion. Little is known about the physiological role of mitochondrial fusion in mammalian development. In addition, the mechanism through which Fzo promotes mitochondrial fusion is unknown. This proposal addresses these issues with the following research goals: (1) to determine the role of mitochondrial fusion in mammalian development through developmental and cellular analysis of mice lacking homologs of Fzo, (2) to gain a detailed understanding of the structural domains of Fzo and the roles these domains play in mediating membrane fusion, (3) to identify other components of the fusion machinery through development of an in vitro mitochondrial fusion assay and isolation of Fzo-associated proteins. In addition to clarifying a basic cellular process, these studies may further understanding of human mitochondrial diseases and aging.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM062967-02
Application #
6520467
Study Section
Cell Development and Function Integrated Review Group (CDF)
Program Officer
Shapiro, Bert I
Project Start
2001-04-01
Project End
2006-03-31
Budget Start
2002-04-01
Budget End
2003-03-31
Support Year
2
Fiscal Year
2002
Total Cost
$246,240
Indirect Cost
Name
California Institute of Technology
Department
Type
Schools of Arts and Sciences
DUNS #
078731668
City
Pasadena
State
CA
Country
United States
Zip Code
91125
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Marinov, Georgi K; Wang, Yun E; Chan, David et al. (2014) Evidence for site-specific occupancy of the mitochondrial genome by nuclear transcription factors. PLoS One 9:e84713
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Chan, Nickie C; den Besten, Willem; Sweredoski, Michael J et al. (2014) Degradation of the deubiquitinating enzyme USP33 is mediated by p97 and the ubiquitin ligase HERC2. J Biol Chem 289:19789-98
Losón, Oliver C; Liu, Raymond; Rome, Michael E et al. (2014) The mitochondrial fission receptor MiD51 requires ADP as a cofactor. Structure 22:367-77

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