COX3 MESSENGER RNA-SPECIFIC TRANSLATIONAL ACTIVATOR PROTEINS ARE ASSOCIATED WITH THE INNER MITOCHONDRIAL-MEMBRANE IN SACCHAROMYCES-CEREVISIAE

Citation
Tw. Mcmullin et Td. Fox, COX3 MESSENGER RNA-SPECIFIC TRANSLATIONAL ACTIVATOR PROTEINS ARE ASSOCIATED WITH THE INNER MITOCHONDRIAL-MEMBRANE IN SACCHAROMYCES-CEREVISIAE, The Journal of biological chemistry, 268(16), 1993, pp. 11737-11741
Citations number
50
Categorie Soggetti
Biology
ISSN journal
00219258
Volume
268
Issue
16
Year of publication
1993
Pages
11737 - 11741
Database
ISI
SICI code
0021-9258(1993)268:16<11737:CMRTAP>2.0.ZU;2-I
Abstract
Three yeast proteins coded by nuclear genes, PET54, PET122, and PET494 , are specifically required to activate translation of the mitochondri ally coded COX3 mRNA, and one of them, PET122, has been shown to inter act functionally with both the mitochondrial ribosomal small subunit a nd the COX3 mRNA leader. To determine the location of these proteins w ithin mitochondria, we have used antisera directed against them to ass ay for their presence in submitochondrial fractions. Approximately hal f of the PET54 protein present in mitochondria from wild-type cells pe lleted with membranes, while half was released from disrupted mitochon dria in soluble form. The membrane-bound PET54 floated with the inner membrane during buoyant density gradient centrifugation, but was effic iently solubilized by extraction with alkaline carbonate. The PET122 a nd PET494 proteins could only be detected in cells overproducing these proteins. PET122 was completely membrane-bound and could not be extra cted with alkaline carbonate. Most of the PET494 protein pelleted with membranes and very little could be solubilized by alkaline carbonate. Both PET122 and PET494 floated with membranes during buoyant density gradient centrifugation. These data suggest the possibility that synth esis of the highly hydrophobic subunit Ill of cytochrome c oxidase is activated by PET54, PET122, and PET494 at the inner mitochondrial memb rane. Amino-terminal sequencing of proteins isolated from mitochondria revealed that PET54 is not processed during import to mitochondria wh ile the PET122 precursor is cleaved between the 8th and 9th residues.