Warzecha Claude C, Sato Trey K, Nabet Behnam, Hogenesch John B, Carstens Russ P
Department of Medicine, Renal Division, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
Mol Cell. 2009 Mar 13;33(5):591-601. doi: 10.1016/j.molcel.2009.01.025.
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.
成纤维细胞生长因子受体2(FGFR2)的上皮和间充质亚型的细胞类型特异性表达分别通过对互斥外显子IIIb和IIIc的严格调控来实现。通过基于细胞的cDNA表达筛选应用,我们鉴定出两种旁系同源的上皮细胞类型特异性RNA结合蛋白,它们是FGFR2剪接的关键调节因子。在表达FGFR2-IIIc的细胞中异位表达任一种蛋白都会导致内源性FGFR2剪接转换为上皮亚型。相反,通过RNA干扰在表达FGFR2-IIIb的细胞中敲低这两种因子会导致从上皮亚型向间充质亚型的转换。这些因子还调节CD44、p120-连环蛋白(CTNND1)和hMena(ENAH)的剪接,这三种转录本在上皮-间充质转化(EMT)过程中剪接会发生变化。这些研究表明,上皮剪接调节蛋白1和2(ESRP1和ESRP2)是上皮细胞类型特异性剪接程序的协调因子。