A bovine trophoblast interferon (IFN-tau) gene promoter sequence (-450
to +26 bp relative to the transcription start site) led to expression
of reporter gene (CAT) constructs transfected into L929 (murine fibro
blast) or JAR (human choriocarcinoma) cells. Expression depended on th
e presence of an exogenous (SV40) enhancer. Poly(I)(C) activated endog
enous IFN production in L929 and JAR cells but had no consistent effec
t on CAT expression. Similar results were obtained in L929 cells with
inactivated Newcastle disease virus. There was no 'priming' effect of
exogenous Type I IFN. Deletion mutants revealed sites exerting negativ
e control on expression between - 338 and - 247 bp, and between - 150
and - 71 bp; these regions contained sequences resembling previously i
dentified negative regulatory domains. In the absence of viral inducib
ility it is proposed that negative regulation contributes towards the
stringent control of expression characteristic of IFN-tau genes.