Brooks Angela N, Duff Michael O, May Gemma, Yang Li, Bolisetty Mohan, Landolin Jane, Wan Ken, Sandler Jeremy, Booth Benjamin W, Celniker Susan E, Graveley Brenton R, Brenner Steven E
Department of Molecular and Cell Biology, University of California, Berkeley, California 94720, USA; Broad Institute, Cambridge, Massachusetts 02142, USA; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts 02215, USA;
Department of Genetics and Genome Sciences, Institute for Systems Genomics, University of Connecticut Health Center, Farmington, Connecticut 06030, USA;
Genome Res. 2015 Nov;25(11):1771-80. doi: 10.1101/gr.192518.115. Epub 2015 Aug 20.
Alternative splicing is regulated by RNA binding proteins (RBPs) that recognize pre-mRNA sequence elements and activate or repress adjacent exons. Here, we used RNA interference and RNA-seq to identify splicing events regulated by 56 Drosophila proteins, some previously unknown to regulate splicing. Nearly all proteins affected alternative first exons, suggesting that RBPs play important roles in first exon choice. Half of the splicing events were regulated by multiple proteins, demonstrating extensive combinatorial regulation. We observed that SR and hnRNP proteins tend to act coordinately with each other, not antagonistically. We also identified a cross-regulatory network where splicing regulators affected the splicing of pre-mRNAs encoding other splicing regulators. This large-scale study substantially enhances our understanding of recent models of splicing regulation and provides a resource of thousands of exons that are regulated by 56 diverse RBPs.
可变剪接受RNA结合蛋白(RBP)调控,这些蛋白识别前体mRNA序列元件并激活或抑制相邻外显子。在此,我们利用RNA干扰和RNA测序来鉴定由56种果蝇蛋白调控的剪接事件,其中一些蛋白此前未知可调控剪接。几乎所有蛋白都影响可变的首个外显子,这表明RBP在首个外显子选择中发挥重要作用。一半的剪接事件受多种蛋白调控,表明存在广泛的组合调控。我们观察到SR蛋白和hnRNP蛋白倾向于协同作用,而非拮抗作用。我们还确定了一个交叉调控网络,其中剪接调节因子影响编码其他剪接调节因子的前体mRNA的剪接。这项大规模研究极大地增进了我们对近期剪接调控模型的理解,并提供了由56种不同RBP调控的数千个外显子的资源。