Effects of myoD and ATF-1 on UCP3 murine promoter activity.
A, luciferase reporter constructs of mouse UCP3 5′-end promoter
region. Numerical annotation is relative to the transcriptional start site
designation as +1. B, reporter constructs transfected into C2C12
myoblasts with MyoD or pcDNA empty control vector. Luciferase activities were
normalized to the activity of 2k-luc co-transfected with the empty vector
(value = 1) and represent mean ± S.D. of three independent experiments
in this and all subsequent cotransfection experiments. C, similar
study to B, with the exception that the luciferase activity in
response to ATF-1 is assessed instead of that of myoD. D,
cotransfection experiments to evaluate the combined ex vivo
activation capacity of myoD and ATF-1 using the full-length and 2-luc UCP3
promoter-luciferase reporter constructs.