Pax3/7-dependent stem cells play an essential role in skeletal muscle development. We now show that Fgfr4 lies genetically downstream from Pax3 and is a direct target. In chromatin immunoprecipitation (ChIP)-on-chip experiments, Pax3 binds to a sequence 3′ of the Fgfr4 gene that directs Pax3-dependent expression at sites of myogenesis in transgenic mouse embryos. The activity of this regulatory element is also partially dependent on E-boxes, targets of the myogenic regulatory factors, which are expressed as progenitor cells enter the myogenic program. Other FGF signaling components, notably Sprouty1, are also regulated by Pax3. In vivo manipulation of Sprouty expression reveals that FGF signaling affects the balance between Pax-positive progenitor cells and committed myoblasts. These results provide new insight into the Pax-initiated regulatory network that modulates stem cell maintenance versus tissue differentiation.
Pax3 regulation of FGF signaling affects the progression of embryonic progenitor cells into the myogenic program
Lagha, M.; Kormish, J. D.; Rocancourt, D.; Manceau, M.; Epstein, J. A.; Zaret, K. S.; Relaix, F.; Buckingham, M. E.
2008-07-01 / vol 22 / pages 1828-37
10.1101/gad.477908 22/13/1828 [pii]
0890-9369 (Print) 0890-9369 (Linking)
IGMM team(s) involved in this publication
Régulation de l’Expression des Gènes au Cours du Développement
Animals; Mice; Signal Transduction; Amino Acid Sequence; Molecular Sequence Data; Cell Differentiation; Paired Box Transcription Factors/*physiology; Adaptor Proteins, Signal Transducing; *Muscle Development; 3' Flanking Region; Embryonic Stem Cells/*cytology/metabolism; Fibroblast Growth Factors/*physiology; Membrane Proteins/metabolism; Myoblasts/*cytology/metabolism; Phosphoproteins/metabolism; Receptor, Fibroblast Growth Factor, Type 4/metabolism; Response Elements