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首页> 外文期刊>Molecular and Cellular Biology >Yeast Pre-mRNA Splicing Requires a Pair of U1 snRNP-Associated Tetratricopeptide Repeat Proteins
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Yeast Pre-mRNA Splicing Requires a Pair of U1 snRNP-Associated Tetratricopeptide Repeat Proteins

机译:酵母前mRNA拼接需要一对U1 snRNP相关的四肽重复蛋白。

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The U1 snRNP functions to nucleate spliceosome assembly on newly transcribed pre-mRNA. Saccharomyces cerevisiae is unusual among eukaryotes in the greatly extended length of its U1 snRNA and the apparent increased polypeptide complexity of the corresponding U1 snRNP. In this paper, we report the identification of a novel U1 snRNP protein, Prp42p, with unexpected properties. Prp42p was identified by its surprising structural similarity to the essential U1 snRNP protein, Prp39p. Both Prp39p and Prp42p possess multiple copies of a variant tetratricopeptide repeat, an element implicated in a wide range of protein assembly events. Yeast strains depleted of Prp42p by transcriptional repression of a GAL1::PRP42fusion gene arrest for splicing prior to pre-mRNA 5′ splice site cleavage. Prp42p was not observed in a recent biochemical analysis of purified U1 snRNPs from S. cerevisiae (28). Nevertheless, antibodies directed against an epitope-tagged version of Prp42p specifically precipitate U1 snRNA from yeast extracts. Furthermore, Prp42p is required for U1 snRNP biogenesis, because yeast strains depleted of Prp42p formed incomplete U1 snRNPs that failed to produce stable complexes with pre-mRNA in vitro. The evidence shows that Prp39p and Prp42p are both required to configure the atypical yeast U1 snRNP into a structure compatible with its evolutionarily conserved role in pre-mRNA splicing.
机译:U1 snRNP的功能是在新转录的pre-mRNA上使剪接体组装成核。酿酒酵母在真核生物中是不寻常的,因为它的U1 snRNA的长度大大延长,并且相应的U1 snRNP的多肽复杂性明显增加。在本文中,我们报告了一种具有意外特性的新型U1 snRNP蛋白Prp42p的鉴定。通过Prp42p与必需的U1 snRNP蛋白Prp39p的惊人结构相似性进行鉴定。 Prp39p和Prp42p都具有变体四肽重复序列的多个副本,该重复序列涉及多种蛋白质组装事件。通过转录抑制 GAL1 :: PRP42 融合基因的转录来抑制Prp42p的酵母菌株,从而在mRNA前5'剪接位点裂解之前进行剪接。在最近从 S纯化的U1 snRNPs的生化分析中未观察到Prp42p。啤酒(28)。然而,针对表位标记版本的Prp42p的抗体可从酵母提取物中特异性沉淀U1 snRNA。此外,U1 snRNP的生物发生需要Prp42p,因为耗尽Prp42p的酵母菌株形成的不完整的U1 snRNPs不能在体外与前mRNA产生稳定的复合物。证据表明,需要使用Prp39p和Prp42p才能将非典型酵母U1 snRNP配置为与其在mRNA前剪接中的进化保守功能兼容的结构。

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