Literature DB >> 19285943

ESRP1 and ESRP2 are epithelial cell-type-specific regulators of FGFR2 splicing.

Claude C Warzecha1, Trey K Sato, Behnam Nabet, John B Hogenesch, Russ P Carstens.   

Abstract

Cell-type-specific expression of epithelial and mesenchymal isoforms of Fibroblast Growth Factor Receptor 2 (FGFR2) is achieved through tight regulation of mutually exclusive exons IIIb and IIIc, respectively. Using an application of cell-based cDNA expression screening, we identified two paralogous epithelial cell-type-specific RNA-binding proteins that are essential regulators of FGFR2 splicing. Ectopic expression of either protein in cells that express FGFR2-IIIc caused a switch in endogenous FGFR2 splicing to the epithelial isoform. Conversely, knockdown of both factors in cells that express FGFR2-IIIb by RNA interference caused a switch from the epithelial to mesenchymal isoform. These factors also regulate splicing of CD44, p120-Catenin (CTNND1), and hMena (ENAH), three transcripts that undergo changes in splicing during the epithelial-to-mesenchymal transition (EMT). These studies suggest that Epithelial Splicing Regulatory Proteins 1 and 2 (ESRP1 and ESRP2) are coordinators of an epithelial cell-type-specific splicing program.

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Year:  2009        PMID: 19285943      PMCID: PMC2702247          DOI: 10.1016/j.molcel.2009.01.025

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  47 in total

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  285 in total

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

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