The CBP protein stimulates transcription of cAMP-responsive genes by b
inding to the phosphorylated activation domain of the CREB transcripti
on factor. Here we show that CBP stimulates transcription of Fos/Jun a
ctivity in F9 cells and that this response is mediated, at least partl
y, via c-Fos, We show that CBP binds c-Fos in a phosphorylation-indepe
ndent manner in vitro, using a domain distinct from that required to b
ind CREB. When this CBP domain is linked to the activation domain of V
P16 it can stimulate GAL4-Fos activity in vivo. The domain of CBP that
binds c-Fos is also used to contact the E1A protein, We therefore ask
ed whether the documented repression of AP1 activity by E1A is due to
sequestration of CBP from c-Fos. We show that E1A 12S can repress c-Fo
s activation functions. The use of E1A mutants indicates that binding
of CBP, but not RB, to E1A is essential for E1A-mediated repression. T
hese data support a model whereby E1A can modulate AP1 activity by dir
ectly competing for the CBP co-activator protein.