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ATP25 a New Nuclear Gene of Saccharomyces cerevisiae Required for Expression and Assembly of the Atp9p Subunit of Mitochondrial ATPase

机译:ATP25酿酒酵母的新核基因表达和组装线粒体ATPase Atp9p亚基所需

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摘要

We report a new nuclear gene, designated ATP25 (reading frame YMR098C on chromosome XIII), required for expression of Atp9p (subunit 9) of the Saccharomyces cerevisiae mitochondrial proton translocating ATPase. Mutations in ATP25 elicit a deficit of ATP9 mRNA and of its translation product, thereby preventing assembly of functional F0. Unlike Atp9p, the other mitochondrial gene products, including ATPase subunits Atp6p and Atp8p, are synthesized normally in atp25 mutants. Northern analysis of mitochondrial RNAs in an atp25 temperature-sensitive mutant confirmed that Atp25p is required for stability of the ATP9 mRNA. Atp25p is a mitochondrial inner membrane protein with a predicted mass of 70 kDa. The primary translation product of ATP25 is cleaved in vivo after residue 292 to yield a 35-kDa C-terminal polypeptide. The C-terminal half of Atp25p is sufficient to stabilize the ATP9 mRNA and restore synthesis of Atp9p. Growth on respiratory substrates, however, depends on both halves of Atp25p, indicating that the N-terminal half has another function, which we propose to be oligomerization of Atp9p into a proper size ring structure.
机译:我们报告了一个新的核基因,称为ATP25(在染色体XIII上的阅读框YMR098C),对于酿酒酵母线粒体质子转运ATPase的Atp9p(9亚基)的表达是必需的。 ATP25中的突变引起ATP9 mRNA及其翻译产物的缺失,从而阻止了功能性F0的装配。与Atp9p不同,其他线粒体基因产物,包括ATPase亚基Atp6p和Atp8p,通常在atp25突变体中合成。对atp25温度敏感突变体中线粒体RNA的Northern分析证实,Apt25p是ATP9 mRNA稳定性所必需的。 Atp25p是线粒体内膜蛋白,预计质量为70 kDa。在残基292之后,体内裂解ATP25的初级翻译产物,以产生35kDa的C末端多肽。 Atp25p的C末端一半足以稳定ATP9 mRNA并恢复Atp9p的合成。但是,在呼吸底物上的生长取决于Atp25p的两半,这表明N末端的另一半具有另一种功能,我们建议将Atp9p寡聚为适当大小的环结构。

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