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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >The Prpl+ Gene Required for Pre-mRNA Splicing in Schizosaccharomyces pombe Encodes a Protein That Contains TPR Motifs and Is Similar to Prp6p of Budding Yeast
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The Prpl+ Gene Required for Pre-mRNA Splicing in Schizosaccharomyces pombe Encodes a Protein That Contains TPR Motifs and Is Similar to Prp6p of Budding Yeast

机译:粟酒裂殖酵母前mRNA剪接所需的Prpl +基因编码一种蛋白质,该蛋白质包含TPR基序,与芽酵母的Prp6p相似

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摘要

The prp (pre-mRNA processing) mutants of the fission yeast Schizosaccharomyces pombe have a defect in pre-mRNA splicing and accumulate mRNA precursors at a restrictive temperature. One of the prp mutants, prp1-4 , also has a defect in poly(A)+ RNA transport. The prp1 + gene encodes a protein of 906 amino acid residues that contains 19 repeats of 34 amino acids termed tetratrico peptide repeat (TPR) motifs, which were proposed to mediate protein-protein interactions. The amino acid sequence of Prplp shares 29.6% identity and 50.6% similarity with that of the PRP6 protein of Saccharomyces cerevisiae , which is a component of the U4/U6 snRNP required for spliceosome assembly. No functional complementation was observed between S. pombe prp1 + and S. cerevisiae PRP6 . We examined synthetic lethality of prp1-4 with the other known prp mutations in S. pombe. The results suggest that Prp1p interacts either physically or functionally with Prp4p, Prp6p and Prp13p. Interestingly, the prp1 + gene was found to be identical with the zer1 + gene that functions in cell cycle control. These results suggest that Prp1p/Zer1p is either directly or indirectly involved in cell cycle progression and/or poly(A)+ RNA nuclear export, in addition to pre-mRNA splicing.
机译:裂变酵母粟酒裂殖酵母的prp(mRNA加工前)突变体在pre-mRNA剪接中存在缺陷,并在限制性温度下积聚mRNA前体。 prp突变体之一prp1-4在poly(A)+ RNA转运中也有缺陷。 prp1 +基因编码一个906个氨基酸残基的蛋白质,该蛋白质包含19个34个氨基酸的重复序列,称为四三肽重复序列(TPR)基序,被提议用来介导蛋白质-蛋白质相互作用。 Prplp的氨基酸序列与酿酒酵母的PRP6蛋白具有29.6%的同一性和50.6%的相似性,所述酿酒酵母是剪接体组装所需的U4 / U6 snRNP的组成部分。没有观察到功能互补之间的粟酒裂殖酵母prp1 +和酿酒酵母PRP6。我们研究了粟酒裂殖酵母中prp1-4与其他已知prp突变的合成杀伤力。结果表明,Prp1p与Prp4p,Prp6p和Prp13p在物理上或功能上相互作用。有趣的是,发现prp1 +基因与在细胞周期控制中起作用的zer1 +基因相同。这些结果表明,除了mRNA前剪接,Prp1p / Zer1p直接或间接参与细胞周期进程和/或poly(A)+ RNA核输出。

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