4.8 Article

An ESRP-regulated splicing programme is abrogated during the epithelial-mesenchymal transition

期刊

EMBO JOURNAL
卷 29, 期 19, 页码 3286-3300

出版社

WILEY
DOI: 10.1038/emboj.2010.195

关键词

alternative splicing; epithelial-mesenchymal transition; epithelial splicing regulatory proteins

资金

  1. NIH [R01-CA093769, R01-GM088809, R01-HG004634]
  2. Edward Mallinckrodt, Jr Foundation [R01-GM085146, T32-GM08216]

向作者/读者索取更多资源

Alternative splicing achieves coordinated changes in post-transcriptional gene expression programmes through the activities of diverse RNA-binding proteins. Epithelial splicing regulatory proteins 1 and 2 (ESRP1 and ESRP2) are cell-type-specific regulators of transcripts that switch splicing during the epithelial-mesenchymal transition (EMT). To define a comprehensive programme of alternative splicing that is regulated during the EMT, we identified an extensive ESRP-regulated splicing network of hundreds of alternative splicing events within numerous genes with functions in cell-cell adhesion, polarity, and migration. Loss of this global ESRP-regulated epithelial splicing programme induces the phenotypic changes in cell morphology that are observed during the EMT. Components of this splicing signature provide novel molecular markers that can be used to characterize the EMT. Bioinformatics and experimental approaches revealed a high-affinity ESRP-binding motif and a predictive RNA map that governs their activity. This work establishes the ESRPs as coordinators of a complex alternative splicing network that adds an important post-transcriptional layer to the changes in gene expression that underlie epithelial-mesenchymal transitions during development and disease. The EMBO Journal (2010) 29, 3286-3300. doi:10.1038/emboj.2010.195; Published online 13 August 2010

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