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

机译:Prp8蛋白的解剖定义了与剪接体催化核心中关键RNA序列的多重相互作用。

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摘要

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.
机译:剪接体核心的当前模型包括涉及前mRNA和U2,U5和U6 snRNA的RNA-RNA相互作用网络。必需的剪接体蛋白Prp8与U5和U6 snRNA以及参与催化作用的特定pre-mRNA序列相互作用。与关键RNA序列的这种紧密联系以及广泛的遗传证据表明,Prp8可以直接影响催化核心的功能,可能充当剪接辅因子。然而,Prp8的序列几乎是全新的,并且它对于Prp8-RNA相互作用的分子基础提供的线索很少。我们已经使用了一种基于转座子的创新策略来建立催化核心RNA在Prp8的中央区域建立多个接触,从而强调了该蛋白质与剪接体催化中心之间的密切关系。我们对RNA相互作用的分析确定了Prp8的离散,高度保守区域是剪接体RNA核心辅因子作用的主要候选对象。

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