The principal goal of this grant proposal is to obtain information about the control of transcription of mitochondrial DNA. The purpose is to gain better insight to the mechanisms that control mitochondrial biogenesis in both the lower and higher eukaryotes. The work is particularly relevant to cardiac tissue in which metabolism is almost completely dependent upon the aerobic synthesis of ATP generated by mitochondria.
Our specific aims are to identify the transcriptional initiation sites of the yeast mitochondrial genes and to sequence these regions to gain information about possible controlling elements. We wil identify mitochondrial transcriptional initiation sites in grande and petite yeast by using the guanylyltransferase reaction, and map initiation sites by hybridiation to restriction enzyme digests of mtDNA. The extent of processing of the 5' terminus will be determined. The 5' flanking regions of different mitochondrial genes will be sequenced to identify homologies which may be essential for regulation of transcription. We will also develop an in vitro transcription system with mitochondrial DNA and mitochondrial RNA polymerase to characterize factors which regulate transcription. Furthermore, we will isolate mutants of mitochondrial RNA polymerase and of other factors participating in the regulation of mitochondrial transcription. We will also examine the biosynthesis of mitochondrial RNA polymerase, the regulation of its transcription, and its role in the control of mitochondrial development. Gene sequences for this enzyme will be isolated and used to evaluate transcription as related to derepression and repression of mitochondrial development.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL004442-27
Application #
3334175
Study Section
Physiological Chemistry Study Section (PC)
Project Start
1977-06-01
Project End
1987-05-31
Budget Start
1985-06-01
Budget End
1986-05-31
Support Year
27
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Chicago
Department
Type
Schools of Medicine
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Sanyal, A; Getz, G S (1995) Import of transcription factor MTF1 into the yeast mitochondria takes place through an unusual pathway. J Biol Chem 270:11970-6
Harington, A; Herbert, C J; Tung, B et al. (1993) Identification of a new nuclear gene (CEM1) encoding a protein homologous to a beta-keto-acyl synthase which is essential for mitochondrial respiration in Saccharomyces cerevisiae. Mol Microbiol 9:545-55
Tung, B S; Unger, E R; Levin, B et al. (1991) Use of an unsaturated fatty acid auxotroph of Saccharomyces cerevisiae to modify the lipid composition and function of mitochondrial membranes. J Lipid Res 32:1025-38
Tonsgard, J H; Tung, B; Kornafel, K S et al. (1990) Environmentally induced differential amplification of mitochondrial populations. Biochem J 270:511-8
Biswas, T K; Getz, G S (1988) Promoter-promoter interactions influencing transcription of the yeast mitochondrial gene, Oli 1, coding for ATPase subunit 9. Cis and trans effects. J Biol Chem 263:4844-51
Ticho, B S; Getz, G S (1988) The characterization of yeast mitochondrial RNA polymerase. A monomer of 150,000 daltons with a transcription factor of 70,000 daltons. J Biol Chem 263:10096-103
Backer, J S; Getz, G S (1987) Identification of a new promoter within the tRNA gene cluster of the mitochondrial DNA of Saccharomyces cerevisiae. Nucleic Acids Res 15:9309-24
Mueller, D M; Biswas, T K; Backer, J et al. (1987) Temperature sensitive pet mutants in yeast Saccharomyces cerevisiae that lose mitochondrial RNA. Curr Genet 11:359-67
Biswas, T K; Ticho, B; Getz, G S (1987) In vitro characterization of the yeast mitochondrial promoter using single-base substitution mutants. J Biol Chem 262:13690-6
Mueller, D M; Getz, G S (1987) Direct determination of the specific activity of RNA uniformly labeled with 32P. Anal Biochem 162:521-8

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