Rbfox proteins regulate tissue-specific alternative splicing of Mef2D required for muscle differentiation

被引:44
作者
Runfola, Valeria [1 ,2 ,3 ]
Sebastian, Soji [4 ]
Dilworth, F. Jeffrey [4 ]
Gabellini, Davide [1 ,2 ]
机构
[1] Ist Sci San Raffaele, Dulbecco Telethon Inst, I-20132 Milan, Italy
[2] Ist Sci San Raffaele, Div Regenerat Med, I-20132 Milan, Italy
[3] Univ Vita Salute San Raffaele, I-20132 Milan, Italy
[4] Ottawa Hosp Res Inst, Sprott Ctr Stem Cell Res, Regenerat Med Program, Ottawa, ON K1Y 4E9, Canada
基金
欧洲研究理事会; 加拿大健康研究院;
关键词
Mef2; Muscle differentiation; Rbfox; Alternative splicing; CELL-DIFFERENTIATION; MYOGENESIS; ISOFORM; FAMILY; ROLES;
D O I
10.1242/jcs.161059
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Among the Mef2 family of transcription factors, Mef2D is unique in that it undergoes tissue-specific splicing to generate an isoform that is essential for muscle differentiation. However, the mechanisms mediating this muscle-specific processing of Mef2D remain unknown. Using bioinformatics, we identified Rbfox proteins as putative modulators of Mef2D muscle-specific splicing. Accordingly, we found direct and specific Rbfox1 and Rbfox2 binding to Mef2D pre-mRNA in vivo. Gain- and loss-of-function experiments demonstrated that Rbfox1 and Rbfox2 cooperate in promoting Mef2D splicing and subsequent myogenesis. Thus, our findings reveal a new role for Rbfox proteins in regulating myogenesis through activation of essential muscle-specific splicing events.
引用
收藏
页码:631 / 637
页数:7
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