ATP synthase of yeast mitochondria -: Isolation of subunit j and disruption of the ATP18 gene

被引:55
作者
Arnold, I
Pfeiffer, K
Neupert, W
Stuart, RA [1 ]
Schägger, H
机构
[1] Univ Munich, Inst Physiol Chem, D-80336 Munich, Germany
[2] Univ Frankfurt Klinikum, Zentrum Biol Chem, D-60590 Frankfurt, Germany
关键词
D O I
10.1074/jbc.274.1.36
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The subunit composition of the mitochondrial ATP synthase from Saccharomyces cerevisiae was analyzed using blue native gel electrophoresis and high resolution SDS-polyacrylamide gel electrophoresis, We report here the identification of a novel subunit of molecular mass of 6,687 Da, termed subunit j (Su j). An open reading frame of 127 base pairs (ATP18), which encodes for Su j, was identified on chromosome XIII. Su j does not display sequence similarity to ATP synthase subunits from other organisms. Data base searches, however, identified a potential homolog from Schizosaccharomyces pombe with 51% identity to Su j of S. cerevisiae. Su j, a small protein of 59 amino acid residues, has the characteristics of an integral inner membrane protein with a single transmembrane segment. Deletion of the ATP18 gene encoding Su j led to a strain (Delta su j) completely deficient in oligomycin-sensitive ATPase activity and unable to grow on nonfermentable carbon sources. The presence of Su j is required for the stable expression of subunits 6 and f of the F-0 membrane sector. In the absence of Su j, spontaneously arising rho(-) cells were observed that lacked also ubiquinol-cytochrome c reductase and cytochrome c oxidase activities. We conclude that Su j is a novel and essential subunit of yeast ATP synthase.
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页码:36 / 40
页数:5
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