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Rpp2, an essential protein subunit of nuclear RNase P, is required for processing of precursor tRNAs and 35S precursor rRNA in Saccharomyces cerevisiae

机译:Rpp2是核糖核酸酶P的必需蛋白亚基,在酿酒酵母中加工前体tRNA和35S前体rRNA是必需的。

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摘要

RPP2, an essential gene that encodes a 15.8-kDa protein subunit of nuclear RNase P, has been identified in the genome of Saccharomyces cerevisiae. Rpp2 was detected by sequence similarity with a human protein, Rpp20, which copurifies with human RNase P. Epitope-tagged Rpp2 can be found in association with both RNase P and RNase mitochondrial RNA processing in immunoprecipitates from crude extracts of cells. Depletion of Rpp2 protein in vivo causes accumulation of precursor tRNAs with unprocessed introns and 5′ and 3′ termini, and leads to defects in the processing of the 35S precursor rRNA. Rpp2-depleted cells are defective in processing of the 5.8S rRNA. Rpp2 immunoprecipitates cleave both yeast precursor tRNAs and precursor rRNAs accurately at the expected sites and contain the Rpp1 protein orthologue of the human scleroderma autoimmune antigen, Rpp30. These results demonstrate that Rpp2 is a protein subunit of nuclear RNase P that is functionally conserved in eukaryotes from yeast to humans.
机译:RPP2是一种编码核糖核酸酶P的15.8-kDa蛋白亚基的必需基因,已在酿酒酵母的基因组中鉴定。通过与人类蛋白Rpp20的序列相似性检测到Rpp2,该蛋白与人RNase P共纯化。带有抗原表位的Rpp2可以与RNase P和RNase线粒体RNA加工同时存在于细胞粗提物中的免疫沉淀物中。 Rpp2蛋白在体内的消耗会导致未加工内含子,5'和3'末端的前体tRNA积累,并导致35S前体rRNA加工过程中的缺陷。缺乏Rpp2的细胞在5.8S rRNA加工中存在缺陷。 Rpp2免疫沉淀物可在预期位点准确切割酵母前体tRNA和前体rRNA,并含有人硬皮病自身免疫抗原Rpp30的Rpp1蛋白直向同源物。这些结果表明,Rpp2是核RNase P的蛋白质亚基,在从酵母到人的真核生物中功能上保守。

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