ERV9 is a low repeated family of human endogenous retroviral elements
whose expression is mainly detectable in undifferentiated embryonal ca
rcinoma NT2/D1 cells. To define all the elements required for the corr
ect transcription activity of the ERV9 promoter and to establish a pre
cise correlation between the elements important for basal transcriptio
n, we have systematically analyzed the in vivo and in vitro transcript
ional activity of many different ERV9 promoter mutants, including a se
ries of linker-scanning mutations across the promoter region. We repor
t here that the ERV9 promoter contains two elements controlling the se
lection of the correct start sites, a TATA box and an Inr-like region;
the concerted action of both elements is necessary for faithful trans
cription. Finally, using a series of GAL4 protein fusion constructs in
cotransfection experiments, we demonstrated that various transcriptio
n factors can synergistically induce a high level of transcription whe
n bound to an ERV9 DNA promoter. (C) 1994 Academic Press, Inc.