This project involves a comprehensive genetic analysis of the regulation of cardiolipin biosynthesis in yeast. A search will be conducted for structural and regulatory mutants affecting this pathway. These newly isolated mutants, as well as existing mutants of phospholipid, sterol, and fatty acid synthesis will be used to analyze the cardiolipin pathway and to ascertain the role of cross-pathway control in the regulation of cardiolipin synthesis. Molecular technology will be employed to clone the genes involved in this pathway in order to establish gene:enzyme relationships, to analyze the role of transcriptional control in the regulation of the pathway, and to identify crucial regulatory sites within the structural genes. The structural and regulatory mutants will be used to study the role of cardiolipin in the development of mitochondria and in the activities essential for mitochondrial function. The information gained in these studies will provide insight into the regulation of membrane biogenesis and the role of phospholipid regulation in the development and function of a complex subcellular organelle. Yeast is amenable to genetic, molecular, and biochemical analyses and is itself a eukaryote which systhesizes cellular and mitochondrial membranes by pathways similar to those of higher organisms. The mitochondrion is a complex organelle which plays a key role in energy metabolism and phospholipid biosynthesis, and is furthermore implicated in processes leading to cellular senescence. The study of mitochondrial membrane biogenesis in this model eukaryote may thus be expected to contribute to our understanding of the role played by the mitochondrion in these processes.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM037723-06
Application #
3293323
Study Section
Physiological Chemistry Study Section (PC)
Project Start
1987-01-01
Project End
1992-12-31
Budget Start
1992-08-01
Budget End
1992-12-31
Support Year
6
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Jiang, F; Kelly, B L; Hagopian, K et al. (1998) Purification and characterization of phosphatidylglycerolphosphate synthase from Schizosaccharomyces pombe. J Biol Chem 273:4681-8
Zhao, M; Schlame, M; Rua, D et al. (1998) Cardiolipin synthase is associated with a large complex in yeast mitochondria. J Biol Chem 273:2402-8
Zhao, M; Rua, D; Hajra, A K et al. (1998) Enzymatic synthesis of [3H]Cytidine 5'-diphospho-1, 2-diacyl-sn-glycerol. Anal Biochem 258:48-52
Jiang, F; Rizavi, H S; Greenberg, M L (1997) Cardiolipin is not essential for the growth of Saccharomyces cerevisiae on fermentable or non-fermentable carbon sources. Mol Microbiol 26:481-91
Schlame, M; Greenberg, M L (1997) Cardiolipin synthase from yeast. Biochim Biophys Acta 1348:201-6
Minskoff, S A; Greenberg, M L (1997) Phosphatidylglycerophosphate synthase from yeast. Biochim Biophys Acta 1348:187-91
Schlame, M; Zhao, M; Rua, D et al. (1995) Kinetic analysis of cardiolipin synthase: a membrane enzyme with two glycerophospholipid substrates. Lipids 30:633-40
Kelly, B L; Greenberg, M L (1994) Expression in yeast of an Escherichia coli gene encoding a phospholipid biosynthetic enzyme. Gene 147:111-4
Minskoff, S A; Racenis, P V; Granger, J et al. (1994) Regulation of phosphatidic acid biosynthetic enzymes in Saccharomyces cerevisiae. J Lipid Res 35:2254-62
Greenberg, M L; Axelrod, D (1993) Anomalously slow mobility of fluorescent lipid probes in the plasma membrane of the yeast Saccharomyces cerevisiae. J Membr Biol 131:115-27

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