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
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.