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核U5小核仁核糖核酸对II组内含子剪接的反式激活作用。

Trans-activation of group II intron splicing by nuclear U5 snRNA.

作者信息

Hetzer M, Wurzer G, Schweyen R J, Mueller M W

机构信息

Vienna Biocenter, Institute of Microbiology and Genetics, University of Vienna, Austria.

出版信息

Nature. 1997 Mar 27;386(6623):417-20. doi: 10.1038/386417a0.

Abstract

Similarities between RNA splicing during autocatalytic excision of group II introns and pre-mRNA processing led to the hypothesis that group II introns might be the evolutionary predecessors of spliceosomal small nuclear RNAs. The ID3 subdomain stem-loop structure of group II introns, the proposed analogue of the spliceosomal U5 snRNA, is thought to be essential for 5' splice site recognition and anchoring of the free 5' exon. Using the group II intron bI1 we have analysed the role of ID3 in splicing. In the absence of ID3 the 5' splice site was recognized accurately and efficiently, but exon anchoring was greatly reduced. This step was restored in the presence of RNA fragments consisting of either the terminal stem-loop structure of ID3 or spliceosomal U5 snRNA. This suggests that the predominant role of both RNAs is to anchor the 5' exon during exon ligation. Furthermore, as U5 complements for the loss of ID3, a similar network of structural RNAs may form the catalytic core of both group II introns and spliceosomes.

摘要

II类内含子自催化切除过程中的RNA剪接与前体mRNA加工之间的相似性,引发了这样一种假说,即II类内含子可能是剪接体小核RNA的进化前身。II类内含子的ID3亚结构域茎环结构被认为是剪接体U5 snRNA的类似物,对5'剪接位点识别和游离5'外显子的锚定至关重要。我们利用II类内含子bI1分析了ID3在剪接中的作用。在没有ID3的情况下,5'剪接位点能够被准确且高效地识别,但外显子锚定却大大减少。在存在由ID3的末端茎环结构或剪接体U5 snRNA组成的RNA片段时,这一步骤得以恢复。这表明这两种RNA的主要作用都是在 exon连接过程中锚定5'外显子。此外,由于U5可弥补ID3的缺失,类似的结构RNA网络可能构成II类内含子和剪接体的催化核心。

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