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上皮剪接因子 ESRP1 和 ESRP2 正向和负向调节多种类型的可变剪接事件。

The epithelial splicing factors ESRP1 and ESRP2 positively and negatively regulate diverse types of alternative splicing events.

机构信息

Renal Division, Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA, USA.

出版信息

RNA Biol. 2009 Nov-Dec;6(5):546-62. doi: 10.4161/rna.6.5.9606. Epub 2009 Nov 22.

Abstract

Cell-type and tissue-specific alternative splicing events are regulated by combinatorial control involving both abundant RNA binding proteins as well as those with more discrete expression and specialized functions. Epithelial Splicing Regulatory Proteins 1 and 2 (ESRP1 and ESRP2) are recently discovered epithelial-specific RNA binding proteins that promote splicing of the epithelial variant of the FGFR2, ENAH, CD44 and CTNND1 transcripts. To catalogue a larger set of splicing events under the regulation of the ESRPs we profiled splicing changes induced by RNA interference-mediated knockdown of ES RP1 and ES RP2 expression in a human epithelial cell line using the splicing sensitive Affymetrix Exon ST1.0 Arrays. Analysis of the microarray data resulted in the identification of over a hundred candidate ESRP regulated splicing events. We were able to independently validate 38 of these targets by RT-PCR. The ESRP regulated events encompass all known types of alternative splicing events, most prominent being alternative cassette exons and splicing events leading to alternative 3' terminal exons. Importantly, a number of these regulated splicing events occur in gene transcripts that encode proteins with well-described roles in the regulation of actin cytoskeleton organization, cell-cell adhesion, cell polarity and cell migration. In sum, this work reveals a novel list of transcripts differentially spliced in epithelial and mesenchymal cells, implying that coordinated alternative splicing plays a critical role in determination of cell type identity. These results further establish ESRP1 and ESRP2 as global regulators of an epithelial splicing regulatory network.

摘要

细胞类型和组织特异性的选择性剪接事件受到组合控制的调节,包括丰富的 RNA 结合蛋白以及那些具有更离散表达和专门功能的蛋白质。上皮剪接调节蛋白 1 和 2(ESRP1 和 ESRP2)是最近发现的上皮特异性 RNA 结合蛋白,它们促进 FGFR2、ENAH、CD44 和 CTNND1 转录物的上皮变体的剪接。为了在 ESRP 的调节下对更大的一组剪接事件进行编目,我们使用剪接敏感的 Affymetrix Exon ST1.0 Arrays 分析了 RNA 干扰介导的 ESRP1 和 ESRP2 表达敲低对人上皮细胞系中剪接变化的影响。微阵列数据分析导致鉴定出一百多个候选 ESRP 调节的剪接事件。我们能够通过 RT-PCR 独立验证其中的 38 个靶标。ESRP 调节的事件包括所有已知类型的选择性剪接事件,最突出的是选择性外显子和导致选择性 3'末端外显子的剪接事件。重要的是,这些调节的剪接事件中的一些发生在基因转录本中,这些转录本编码在调节肌动蛋白细胞骨架组织、细胞间黏附、细胞极性和细胞迁移方面具有明确作用的蛋白质。总之,这项工作揭示了上皮细胞和间充质细胞中差异剪接的新转录本列表,这表明协调的选择性剪接在确定细胞类型身份方面起着关键作用。这些结果进一步确立了 ESRP1 和 ESRP2 作为上皮剪接调节网络的全局调节剂。

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本文引用的文献

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