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Coupling between alternative polyadenylation and alternative splicing is limited to terminal introns

机译:替代聚腺苷酸化和选择性剪接之间的偶联仅限于末端内含子

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摘要

Alternative polyadenylation has been implicated as an important regulator of gene expression. In some cases, alternative polyadenylation is known to couple with alternative splicing to influence last intron removal. However, it is unknown whether alternative polyadenylation events influence alternative splicing decisions at upstream exons. Knockdown of the polyadenylation factors CFIm25 or CstF64 in HeLa cells was used as an approach in identifying alternative polyadenylation and alternative splicing events on a genome-wide scale. Although hundreds of alternative splicing events were found to be differentially spliced in the knockdown of CstF64, genes associated with alternative polyadenylation did not exhibit an increased incidence of alternative splicing. These results demonstrate that the coupling between alternative polyadenylation and alternative splicing is usually limited to defining the last exon. The striking influence of CstF64 knockdown on alternative splicing can be explained through its effects on UTR selection of known splicing regulators such as hnRNP A2/B1, thereby indirectly influencing splice site selection. We conclude that changes in the expression of the polyadenylation factor CstF64 influences alternative splicing through indirect effects.
机译:牵连的聚腺苷酸化被认为是基因表达的重要调节剂。在某些情况下,已知替代性聚腺苷酸化与替代性剪接相结合以影响最后内含子的去除。然而,尚不清楚替代的聚腺苷酸化事件是否影响上游外显子的替代剪接决定。击倒HeLa细胞中的聚腺苷酸化因子CFIm25或CstF64被用作在全基因组范围内鉴定替代性聚腺苷酸化和替代性剪接事件的方法。尽管发现数百个替代剪接事件在CstF64的敲低中被不同程度地剪接,但是与替代聚腺苷酸化相关的基因并未显示替代剪接的发生率增加。这些结果表明,可替代的聚腺苷酸化和可替代的剪接之间的偶联通常限于限定最后一个外显子。 CstF64敲除对替代剪接的显着影响可以通过其对已知剪接调节子(如hnRNP A2 / B1)的UTR选择的影响来解释,从而间接影响剪接位点的选择。我们得出的结论是,聚腺苷酸化因子CstF64表达的变化通过间接作用影响了选择性剪接。

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