Figure 3

PAX7 promoter activity modulated by the 10-bp indel polymorphism. (A) Luciferase activity in C2C12 cells transfected with recombinant plasmids containing serial promoter fragments (pGL3-pro1, pGL3-pro2, pGL3-pro3, pGL3-pro4, and pGL3-pro5) of the Pax7 promoter. The backbone vector pGL3-Basic was used as a negative control. PpGL3-pro2 vs. pGL3-pro1ā=ā0.0118, PpGL3-pro2 vs. pGL3-pro3ā=ā0.0042, PpGL3-pro2 vs. pGL3-pro4ā=ā0.0495, PpGL3-pro2 vs. pGL3-pro5ā=ā0.0241. (B) Luciferase activity in C2C12 cells transfected with recombinant plasmids containing the Ins-Ins or Del-Del genotype. pcDNA3.1-ZNF219 was transiently co-transfected into C2C12 cells together with the reporter vectors. Each experiment was repeated at least three times. The data were meanā±āstandard error (S.E.) of the normalized luciferase activity. *Pā<ā0.05 represents a significant difference.