TERMINAL differentiation and cell proliferation are in many cases, as
in muscle cells1, mutually exclusive processes. While differentiating
myoblasts are withdrawn from the cell cycle2, myogenesis is inhibited
by some mitogens and overexpression of some oncogenes3,4, including pr
oto-oncogene c-fos5 (which expresses a growth-associated protein const
ituting the regulatory factor AP-1 in conjunction with c-Jun6,7). MyoD
, a muscle-specific transcription factor of the basic helix-loop-helix
family8,9, acts at both levels because it triggers a muscle different
iation programme in non-muscle cells10-12, and induces a complete bloc
k of cell proliferation13,14. Antagonistic interaction between MyoD an
d c-Jun has been demonstrated15. We here show that c-fos expression gr
eatly decreases upon muscle cell differentiation, concomitant with Myo
D-induced activity. We have identified a MyoD-binding site overlapping
with the serum-responsive element in the c-fos promoter. We demonstra
te that MyoD can act as a negative regulator for c-fos transcription b
y blocking serum responsiveness through this binding site. These data
suggest that the MyoD negative effect on cell growth could be partly m
ediated by transcriptional inactivation of growth-responsive genes.