首页> 美国卫生研究院文献>The EMBO Journal >Identification and characterization of Uss1p (Sdb23p): a novel U6 snRNA-associated protein with significant similarity to core proteins of small nuclear ribonucleoproteins.
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Identification and characterization of Uss1p (Sdb23p): a novel U6 snRNA-associated protein with significant similarity to core proteins of small nuclear ribonucleoproteins.

机译:Uss1p(Sdb23p)的鉴定和表征:一种新颖的U6 snRNA相关蛋白,与小核核糖核蛋白的核心蛋白具有显着相似性。

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摘要

The SDB23 gene of Saccharomyces cerevisiae was isolated in a search for high copy-number suppressors of mutations in a cell cycle gene, DBF2, SDB23 encodes a 21,276 Da protein with significant sequence similarity to characterized mammalian snRNP core proteins. Examination of multiple sequence alignments of snRNP core proteins with Sdb23p indicates that all of these proteins share a number of highly conserved residues, and identifies a novel motif for snRNP core proteins. Sdb23p is essential for cell viability and is required for nuclear pre-mRNA splicing both in vivo and in vitro. Extracts prepared from Sdb23p-depleted cells are unable to support splicing and have vastly reduced levels of U6 snRNA. The stability of U1, U2, U4 and U5 spliceosomal snRNAs is not affected by the loss of Sdb23p. Antibodies raised against Sdb23p strongly coimmunoprecipitate free U6 snRNA and U4/U6 base-paired snRNAs. These results establish that SDB23 encodes a novel U6 snRNA-associated protein that is essential for the stability of U6 snRNA. We therefore propose the more logical name USS1 (U-Six SnRNP) for this gene.
机译:为了在细胞周期基因DBF2中寻找突变的高拷贝数抑制子,分离了酿酒酵母的SDB23基因,SDB23编码一个21,276 Da的蛋白质,该蛋白质与特征性哺乳动物snRNP核心蛋白质具有显着的序列相似性。 snRNP核心蛋白与Sdb23p的多重序列比对检验表明,所有这些蛋白都共享许多高度保守的残基,并确定了snRNP核心蛋白的新基序。 Sdb23p对于细胞活力至关重要,并且是体内和体外核前mRNA剪接所必需的。从耗尽Sdb23p的细胞制备的提取物无法支持剪接,并且U6 snRNA的水平大大降低。 U1,U2,U4和U5剪接体snRNA的稳定性不受Sdb23p丢失的影响。针对Sdb23p产生的抗体可强烈共免疫沉淀游离的U6 snRNA和U4 / U6碱基配对的snRNA。这些结果表明,SDB23编码一种新型的U6 snRNA相关蛋白,对U6 snRNA的稳定性至关重要。因此,我们为该基因提出了更合乎逻辑的名称USS1(U-Six SnRNP)。

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