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Spatial Organization of Protein-RNA Interactions in the Branch Site-3′ Splice Site Region during pre-mRNA Splicing in Yeast

机译:酵母前mRNA剪接过程中分支Site-3剪接位点区域中蛋白质-RNA相互作用的空间组织。

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摘要

A series of efficiently spliced pre-mRNA substrates containing single 4-thiouridine residues were used to monitor RNA-protein interactions involving the branch site-3′ splice site-3′ exon region during yeast pre-mRNA splicing through cross-linking analysis. Prior to the assembly of the prespliceosome, Mud2p and the branch point bridging protein cross-link to a portion of this region in an ATP-independent fashion. Assembly of the prespliceosome leads to extensive cross-linking of the U2-associated protein Hsh155p to this region. Following the first step of splicing and in a manner independent of Prp16p, the U5 small nuclear ribonucleoprotein particle-associated protein Prp8p also associates extensively with the branch site-3′ splice site-3′ exon region. The subsequent cross-linking of Prp16p to the lariat intermediate is restricted to the 3′ splice site and the adjacent 3′ exon sequence. Using modified substrates to either mutationally or chemically block the second step, we found that the association of Prp22p with the lariat intermediate represents an authentic transient intermediate and appears to be restricted to the last eight intron nucleotides. Completion of the second step leads to the cross-linking of an unidentified ∼80-kDa protein near the branch site sequence, suggesting a potential role for this protein in a later step in intron metabolism. Taken together, these data provide a detailed portrayal of the dynamic associations of proteins with the branch site-3′ splice site region during spliceosome assembly and catalysis.
机译:通过交联分析,在酵母pre-mRNA剪接过程中,使用一系列包含单个4-硫尿苷残基的有效剪接的pre-mRNA底物来监测涉及分支位点3'剪接位点3'外显子区域的RNA-蛋白质相互作用。在组装前剪接体之前,Mud2p和分支点桥接蛋白以不依赖ATP的方式交联到该区域的一部分。前剪接体的组装导致U2相关蛋白Hsh155p与该区域的广泛交联。剪接的第一步之后,并且以独立于Prp16p的方式,U5小核糖核蛋白颗粒相关蛋白Prp8p也与分支位点3'剪接位点3'外显子区域广泛缔合。 Prp16p随后与套索中间体的交联仅限于3'剪接位点和相邻的3'外显子序列。使用修饰的底物以突变方式或化学方式阻断第二步,我们发现Prp22p与套索中间体之间的缔合代表了真正的瞬时中间体,并且似乎仅限于最后八个内含子核苷酸。第二步的完成导致分支位点序列附近的一个未鉴定的〜80 kDa蛋白交联,表明该蛋白在内含子代谢的后续步骤中可能发挥作用。综上所述,这些数据提供了在剪接体组装和催化过程中蛋白质与分支部位3'剪接部位区域之间动态关联的详细描述。

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