Autoregulation of the xC/EBPα promoter. The three xC/EBPα promoter constructs, –1131/+41, –634/+41
and –321/+41, were co-transfected into Hep3B
or A6 cell lines along with recombinant plasmid DNA driving the
expression of either xC/EBPα (+α), the LAP form of xC/EBPβ (+β)
or the pCS2+ vector (+vec). The relative luciferase
activity obtained using the promoter-less pGL2-Basic vector, in
the absence or the presence of the various pCS2+ plasmids,
was subtracted from the corresponding values obtained using the
xC/EBPα promoter constructs.
The normalised activity for each of these promoter constructs alone (–)
has arbitrarily been assigned as 1, with those obtained in the presence
of the co-transfected expression plasmids being shown as fold induction
with respect to this value. Each value represents the mean ± SD
from three to four independent experiments.