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对Prp8蛋白的剖析揭示了其与剪接体催化核心中关键RNA序列的多种相互作用。

Dissection of Prp8 protein defines multiple interactions with crucial RNA sequences in the catalytic core of the spliceosome.

作者信息

Turner Ian A, Norman Christine M, Churcher Mark J, Newman Andrew J

机构信息

MRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK.

出版信息

RNA. 2006 Mar;12(3):375-86. doi: 10.1261/rna.2229706. Epub 2006 Jan 23.

Abstract

Current models of the core of the spliceosome include a network of RNA-RNA interactions involving the pre-mRNA and the U2, U5, and U6 snRNAs. The essential spliceosomal protein Prp8 interacts with U5 and U6 snRNAs and with specific pre-mRNA sequences that participate in catalysis. This close association with crucial RNA sequences, together with extensive genetic evidence, suggests that Prp8 could directly affect the function of the catalytic core, perhaps acting as a splicing cofactor. However, the sequence of Prp8 is almost entirely novel, and it offers few clues to the molecular basis of Prp8-RNA interactions. We have used an innovative transposon-based strategy to establish that catalytic core RNAs make multiple contacts in the central region of Prp8, underscoring the intimate relationship between this protein and the catalytic center of the spliceosome. Our analysis of RNA interactions identifies a discrete, highly conserved region of Prp8 as a prime candidate for the role of cofactor for the spliceosome's RNA core.

摘要

剪接体核心的当前模型包括一个涉及前体信使核糖核酸(pre-mRNA)以及U2、U5和U6小核核糖核酸(snRNA)的核糖核酸-核糖核酸相互作用网络。重要的剪接体蛋白Prp8与U5和U6 snRNA以及参与催化的特定前体信使核糖核酸序列相互作用。与关键核糖核酸序列的这种紧密关联,再加上大量遗传学证据,表明Prp8可能直接影响催化核心的功能,也许作为一种剪接辅因子发挥作用。然而,Prp8的序列几乎完全是全新的,并且它几乎没有为Prp8-核糖核酸相互作用的分子基础提供线索。我们使用了一种基于转座子的创新策略来确定催化核心核糖核酸在Prp8的中央区域进行多次接触,这突出了该蛋白与剪接体催化中心之间的密切关系。我们对核糖核酸相互作用的分析确定了Prp8的一个离散的、高度保守的区域,作为剪接体核糖核酸核心辅因子作用的主要候选区域。

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