Author/Authors :
Graziella Messina، نويسنده , , Stefano Biressi، نويسنده , , Stefania Monteverde، نويسنده , , Alessandro Magli، نويسنده , , Marco Cassano، نويسنده , , Laura Perani، نويسنده , , Elena Roncaglia، نويسنده , , Enrico Tagliafico، نويسنده , , Linda Starnes، نويسنده , , Christine E. Campbell، نويسنده , , Milena Grossi، نويسنده , , David J. Goldhamer، نويسنده , , Richard M. Gronostajski، نويسنده , , Giulio Cossu، نويسنده ,
Abstract :
Skeletal myogenesis, like hematopoiesis, occurs in successive developmental stages that involve different cell populations and expression of different genes. We show here that the transcription factor nuclear factor one X (Nfix), whose expression is activated by Pax7 in fetal muscle, in turn activates the transcription of fetal specific genes such as MCK and β-enolase while repressing embryonic genes such as slow myosin. In the case of the MCK promoter, Nfix forms a complex with PKC theta that binds, phosphorylates, and activates MEF2A. Premature expression of Nfix activates fetal and suppresses embryonic genes in embryonic muscle, whereas muscle-specific ablation of Nfix prevents fetal and maintains embryonic gene expression in the fetus. Therefore, Nfix acts as a transcriptional switch from embryonic to fetal myogenesis.