Because of its critical role in the control of cell proliferation and
differentiation, we postulated that E2F-1 could have a role in murine
development, To this end, the organ and developmental expression of th
e E2F-1 transcription factor was analyzed from midgestation to late-st
age embryogenesis. We demonstrate that the mRNA levels for E2F-1 and i
ts heterodimeric partner DP-1 reach maximal levels in the late embryon
ic and early postnatal period but decline in the later postnatal and a
dult periods, Additionally, using high resolution in situ hybridizatio
n, high expression of E2F-1 was observed in specific cells of individu
al tissues, suggesting that the role of E2F-1 may be more complex than
previously indicated from cell culture studies. Furthermore, the unus
ual pattern of E2F-1 and DP-1 developmental expression may have an ess
ential role in certain cells and tissues in the late embryonic and ear
ly postnatal period.