cdc2 gene expression is under the control of multiple factors. Although E2F
/DP proteins have been reported to play a central role, they cannot account
for all aspects of the fine modulation of cdc2 gene expression during cell
cycle and embryonic development. To characterize the transcription factors
that control cdc2 gene expression during nerve cell differentiation in avi
ans, we have previously cloned the quail cdc2 gene promoter region. We had
identified an octamer (CAGGTGGC) containing an E-box, which has important a
ctivity in regulating cdc2 transcription. Using lit vivo genomic footprinti
ng experiments, we show here that this motif, currently named TG, is the ta
rget of binding proteins at different stages of neuroretina development, co
nfirming its importance as a regulatory response element for cdc2 gene expr
ession. A subset of Helix-Loop-Helix family of transcription factors, known
as Upstream Stimulatory Factors (USFs) specifically bind to this sequence
as dimers, Moreover, our results indicate that USFs transactivate the promo
ter of cdc2 via the IG motif, These data may help to better understand the
mechanisms that control cell division in differentiating nerve cells.