The overall objective of the proposed research is to elucidate the mechanism of protein biosynthesis in the mitochondria of animal cells and to compare this system to prokaryotic and eukaryotic cytoplasmic translational systems. During the past year, we have detected and partially purified the factor responsible for the binding of aminoacyltRNA to mitochondrial ribosomes (mtEF- Tu). We plan to complete the purification of this factor and to carry out a detailed characterization of its mechanism of action. In particular, we will examine the interaction mtEF-Tu with aminoacyltRNA, guanine nucleotides and ribosomes and its sensitivity to specific antibiotics. In addition, we will seek to determine whether a separate factor (analogous to the bacterial factor EFTs) is required to facilitate guanine nucleotide exchange during the recycling of mtEFTu. We have recently detected and partially purified the factor that catalyzes the translocation step of protein synthesis in mitochondria (mtEF-G). We plan to complete the purification of mtEFG and to examine its properties in detail. In this aspect of the proposed research, we hope to define the nature of the elongation cycle in mitochondria and to understand its relationship to the corresponding process in prokaryotes and in the eukaryotic cell cytoplasm. The second major focus of the proposed research is to begin an investigation into the process of protein chain initiation in animal mitochondria. In order to carry out this objective, we will seek to identify the factors required for chain initiation, examine their properties and define their roles in the initiation process. We will seek to determine how the 5' end of the mRNA is recognized as the initiation signal on mitochondrial messenger RNAs. The results obtained will permit us to compare the process of protein chain initiation in this essential cell organelle to other cellular and organelle systems. A longterm objective is to develop a defined in vitro protein synthesizing system from animal cell mitochondria in which to study the regulation of organelle protein synthesis and its integration into the complex metabolism of the eukaryotic cell.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM032734-06
Application #
3281813
Study Section
Physiological Chemistry Study Section (PC)
Project Start
1984-05-01
Project End
1992-04-30
Budget Start
1989-05-01
Budget End
1990-04-30
Support Year
6
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
Schools of Arts and Sciences
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Nallagatla, Subba Rao; Jones, Christie N; Ghosh, Saikat Kumar B et al. (2013) Native tertiary structure and nucleoside modifications suppress tRNA's intrinsic ability to activate the innate immune sensor PKR. PLoS One 8:e57905
Christian, Brooke E; Spremulli, Linda L (2012) Mechanism of protein biosynthesis in mammalian mitochondria. Biochim Biophys Acta 1819:1035-54
Bilbille, Yann; Gustilo, Estella M; Harris, Kimberly A et al. (2011) The human mitochondrial tRNAMet: structure/function relationship of a unique modification in the decoding of unconventional codons. J Mol Biol 406:257-74
Haque, Md Emdadul; Koc, Hasan; Cimen, Huseyin et al. (2011) Contacts between mammalian mitochondrial translational initiation factor 3 and ribosomal proteins in the small subunit. Biochim Biophys Acta 1814:1779-84
Christian, Brooke E; Haque, Md Emdadul; Spremulli, Linda L (2010) The effect of spermine on the initiation of mitochondrial protein synthesis. Biochem Biophys Res Commun 391:942-6
Akama, Kenta; Christian, Brooke E; Jones, Christie N et al. (2010) Analysis of the functional consequences of lethal mutations in mitochondrial translational elongation factors. Biochim Biophys Acta 1802:692-8
Haque, Md Emdadul; Elmore, Kevin B; Tripathy, Ashutosh et al. (2010) Properties of the C-terminal tail of human mitochondrial inner membrane protein Oxa1L and its interactions with mammalian mitochondrial ribosomes. J Biol Chem 285:28353-62
Haque, Md Emdadul; Spremulli, Linda L; Fecko, Christopher J (2010) Identification of protein-protein and protein-ribosome interacting regions of the C-terminal tail of human mitochondrial inner membrane protein Oxa1L. J Biol Chem 285:34991-8
Christian, Brooke E; Spremulli, Linda L (2010) Preferential selection of the 5'-terminal start codon on leaderless mRNAs by mammalian mitochondrial ribosomes. J Biol Chem 285:28379-86
Christian, Brooke E; Spremulli, Linda L (2009) Evidence for an active role of IF3mt in the initiation of translation in mammalian mitochondria. Biochemistry 48:3269-78

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