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IDENTIFICATION OF THE YEAST NUCLEAR GENE FOR THE MITOCHONDRIAL HOMOLOGUE OF BACTERIAL RIBOSOMAL PROTEIN L16

机译:细菌核糖体蛋白L16线粒体同源性的酵母核基因鉴定

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摘要

An open reading frame encoding a member of the L16 family of ribosomal proteins is adjacent to the URA7 gene on the left arm of chromosome II in Saccharomyces cerevisiae. The predicted L16-like polypeptide is basic (pI 11.12), contains 232 amino acids (26.52 kDa) and has 36% amino acid sequence identity to E. coli L16. Immunoblot analysis with polyclonal antibodies to the L16-like polypeptide showed specific crossreaction with a 22 000 Mr mitochondrial polypeptide that co-sediments with the large subunit of the mitochondrial ribosome in sucrose density gradients. The levels of the L16 mRNA and protein varied in response to carbon source. In [rho(o)] cells lacking mitochondrial rRNA, the L16 mRNA accumulated at normal levels, but the protein was barely detectable, indicating RNA-dependent accumulation of the L16 protein. Gene disruption experiments demonstrated that the yeast mitochondrial L16 is an essential ribosomal protein in vivo.
机译:在酿酒酵母中,编码核糖体蛋白L16家族成员的开放阅读框与II号染色体左臂上的URA7基因相邻。预测的L16样多肽是碱性的(pI 11.12),包含232个氨基酸(26.52 kDa),与大肠杆菌L16具有36%的氨基酸序列同一性。用针对L16样多肽的多克隆抗体进行的免疫印迹分析显示与22 000 Mr线粒体多肽发生了特异性交叉反应,该线粒体与线粒体核糖体的大亚基在蔗糖密度梯度中共同沉淀。 L16 mRNA和蛋白质的水平随碳源而变化。在缺乏线粒体rRNA的[rho(o)]细胞中,L16 mRNA积累在正常水平,但几乎无法检测到该蛋白,表明L16蛋白的RNA依赖性积累。基因破坏实验表明,酵母线粒体L16是体内必需的核糖体蛋白。

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