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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,用于表达和组装线粒体ATPase Atp9p亚基

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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 F-o. 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),用于酿酒酵母线粒体质子转运ATPase的Atp9p(9亚基)的表达。 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F-o的组装。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是一种线粒体内膜蛋白,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。然而,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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