Effect of overexpression of Jun and Fos proteins
on TRE-, hARE-, and mutant hARE-mediated CAT gene expression.
(A) The Hep-G2 cells were cotransfected with 10 μg of
reporter plasmids TRE–tk–CAT (Left), hARE–tk–CAT
(Center), and mutant hARE–tk–CAT
(Right) with 10 μg of expression plasmids LNCX,
LNCX–Jun and LNCX–c-Fos individually and in combinations as shown in
separate experiments. The LNCX–c-Fos was also used in different
concentrations (μg). (B) HeLa and F9 cells were
cotransfected with 10 μg of reporter plasmid hARE–tk–CAT and
different concentration of c-Fos expression plasmid LNCX–c-Fos. Five
micrograms of RSV–β-gal plasmid was included in each case as
internal control of transfection efficiency. Forty-eight hours after
transfection, the cells were analyzed for β-gal and CAT activities.