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U1、U2以及U4/U6小核核糖核蛋白是体外剪接所必需的,但不是聚腺苷酸化所必需的。

U1, U2, and U4/U6 small nuclear ribonucleoproteins are required for in vitro splicing but not polyadenylation.

作者信息

Berget S M, Robberson B L

出版信息

Cell. 1986 Aug 29;46(5):691-6. doi: 10.1016/0092-8674(86)90344-2.

Abstract

The requirement for individual U RNAs in splicing and polyadenylation was investigated using oligonucleotide-directed cleavage of snRNAs in in vitro processing extracts. Cleavage of U1, U2, or U4 RNA inhibited splicing but not polyadenylation of short precursor RNAs. Thus each snRNA and the snRNP in which it is assembled participates in the splicing reaction. Splicing activity was recovered when extracts containing cleaved U RNAs were mixed in pairwise combinations, indicating that U1, U2, and U4/U6 snRNPs independently interact with the assembling spliceosome. The involvement of multiple snRNPs in the splicing of simple precursor RNAs suggests that the spliceosome is a large complex assembly consisting of multiple snRNPs whose activity is dependent on the structural integrity of the individual U RNAs.

摘要

利用寡核苷酸定向切割体外加工提取物中的小核仁核糖核酸(snRNAs),研究了个体U RNA在剪接和聚腺苷酸化中的需求。U1、U2或U4 RNA的切割抑制了短前体RNA的剪接,但不影响其聚腺苷酸化。因此,每个小核仁核糖核酸及其组装形成的小核仁核糖核蛋白颗粒(snRNP)都参与剪接反应。当含有切割后的U RNA的提取物以两两组合的方式混合时,剪接活性得以恢复,这表明U1、U2和U4/U6 snRNP能独立地与正在组装的剪接体相互作用。多个snRNP参与简单前体RNA的剪接,这表明剪接体是一个由多个snRNP组成的大型复合组装体,其活性依赖于各个U RNA的结构完整性。

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