Sp3 controls fibroblast growth factor receptor 4 gene activity during myogenic differentiation

• Published in: Gene Vol. 617; pp. 24 - 31
• Main Authors: Cavanaugh, Eric, DiMario, Joseph X.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 20.06.2017
• Subjects: Animals; Cell Differentiation; Cell Line; Differentiation; Mice; Myoblasts - cytology; Myoblasts - metabolism; Myogenesis; Proliferation; Promoter Regions, Genetic; Protein Binding; Receptor, Fibroblast Growth Factor, Type 4 - genetics; Receptor, Fibroblast Growth Factor, Type 4 - metabolism; Sp3 Transcription Factor - genetics; Sp3 Transcription Factor - metabolism; AP2; TSS; GM; DM; Proliferation; GCF; Differentiation; FGFR4; ChIP; Myogenesis; bp
• ISSN: 0378-1119; 1879-0038
• DOI: 10.1016/j.gene.2017.03.039

Fibroblast growth factor/fibroblast growth factor receptor (FGF/FGFR) signaling is a critical component in the regulation of myoblast proliferation and differentiation. The transient FGFR4 gene expression during the transition from proliferating myoblasts to differentiated myotubes indicates that FGFR4 regulates this critical phase of myogenesis. The Specificity Protein (SP) family of transcription factors controls FGFR family member gene activity. We sought to determine if members of the Sp family regulate mouse FGFR4 gene activity during myogenic differentiation. RT-PCR and western blot analysis of FGFR4 mRNA and protein revealed transient expression over 72h, with peak expression between 24 and 36h after addition of differentiation medium to C2C12 myogenic cultures. Sp3 also displayed a transient expression pattern with peak expression occurring after 6h of differentiation. We cloned a 1527bp fragment of the mouse FGFR4 promoter into a luciferase reporter. This FGFR4 promoter contains eight putative Sp binding sites and directed luciferase gene activity comparable to native FGFR4 expression. Overexpression of Sp1 and Sp3 showed that Sp1 repressed FGFR4 gene activity, and Sp3 activated FGFR4 gene activity during myogenic differentiation. Mutational analyses of multiple Sp binding sites within the FGFR4 promoter revealed that three of these sites were transcriptionally active. Electromobility shift assays and chromatin immunoprecipitation of the area containing the activator sites showed that Sp3 bound to this promoter location. •FGFR4 is transiently expressed during myogenic differentiation.•Sp3 binds to an FGFR gene regulatory site.•Sp3 activates the FGFR4 promoter.