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可变聚腺苷酸化与可变剪接之间的偶联仅限于末端内含子。

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

作者信息

Movassat Maliheh, Crabb Tara L, Busch Anke, Yao Chengguo, Reynolds Derrick J, Shi Yongsheng, Hertel Klemens J

机构信息

a Department of Microbiology and Molecular Genetics , School of Medicine, University of California , Irvine , CA , USA.

b Institute of Molecular Biology (IMB) , Mainz , Germany.

出版信息

RNA Biol. 2016 Jul 2;13(7):646-55. doi: 10.1080/15476286.2016.1191727. Epub 2016 May 31.

Abstract

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.

摘要

可变聚腺苷酸化被认为是基因表达的重要调节因子。在某些情况下,已知可变聚腺苷酸化与可变剪接相结合,以影响最后一个内含子的去除。然而,尚不清楚可变聚腺苷酸化事件是否会影响上游外显子的可变剪接决定。在HeLa细胞中敲低聚腺苷酸化因子CFIm25或CstF64被用作在全基因组范围内鉴定可变聚腺苷酸化和可变剪接事件的一种方法。尽管在敲低CstF64时发现数百个可变剪接事件存在差异剪接,但与可变聚腺苷酸化相关的基因并未表现出可变剪接发生率的增加。这些结果表明,可变聚腺苷酸化和可变剪接之间的偶联通常仅限于确定最后一个外显子。敲低CstF64对可变剪接的显著影响可以通过其对已知剪接调节因子(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。我们得出结论,聚腺苷酸化因子CstF64表达的变化通过间接作用影响可变剪接。

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