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首页> 外文期刊>Nucleic acids research >Human RNA lariat debranching enzyme cDNA complements the phenotypes of Saccharomyces cerevisiae dbr1 and Schizosaccharomyces pombe dbr1 mutants
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Human RNA lariat debranching enzyme cDNA complements the phenotypes of Saccharomyces cerevisiae dbr1 and Schizosaccharomyces pombe dbr1 mutants

机译:人类RNA套索脱支酶cDNA互补酿酒酵母dbr1和粟酒裂殖酵母dbr1突变体的表型

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The cDNA encoding the human RNA lariat debranching enzyme (hDBR1) was identified and cloned by searching the Expressed Sequence Tag (EST) database and screening a HeLa cDNA library, based on predicted amino acid sequence homologies with the Saccharomyces cerevisiae, Schizosaccharomyces pombe and Caenorhabditis elegans debranching enzymes. The hDBR1 cDNA expressed in Escherichia coli showed debranching activity in vitro and was also shown to be functional in an interspecies specific complementation experiment. hDBR1 cDNA in a S.cerevisiae expression vector complemented the intron accumulation phenotype of a S.cerevisiae dbr1 null mutant. Integration of the cDNA for hDBR1 into the ura4 locus of S.pombe also complemented both the intron accumulation and slow growth phenotypes of a S.pombe dbr1 null mutant strain. Comparison of the amino acid sequence of hDBR1 with the other DBR protein sequences showed several conserved regions, with 40, 44 and 43% identity to the S.cerevisiae, S.pombe and C.elegans debranching enzymes, respectively.
机译:通过搜索表达序列标签(EST)数据库并筛选HeLa cDNA文库来鉴定和克隆编码人RNA套索脱支酶(hDBR1)的cDNA,基于与酿酒酵母,粟酒裂殖酵母和秀丽隐杆线虫的预测氨基酸序列同源性。脱支酶。在大肠杆菌中表达的hDBR1 cDNA在体外显示脱支活性,并且在种间特异性互补实验中也显示其功能。酿酒酵母表达载体中的hDBR1 cDNA补充了酿酒酵母dbr1空突变体的内含子积累表型。 hDBR1的cDNA整合到S.pombe ura4基因座中也补充了S.pombe dbr1 null突变株的内含子积累和慢速生长表型。 hDBR1氨基酸序列与其他DBR蛋白序列的比较显示了几个保守区,分别与酿酒酵母,粟酒裂殖酵母和秀丽隐杆线虫脱支酶具有40%,44%和43%的同一性。

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