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Human Prolactin Gene Promoter Regulation by Estrogen: Convergence with Tumor Necrosis Factor- Signaling

Endocrine Sciences Research Group (A.D.A., S.F., J.R.E.D.), University of Manchester, Manchester M13 9NT, United Kingdom; Molecular Physiology (S.S., J.J.M.), University of Edinburgh, Edinburgh EH8 9XP, United Kingdom; and Centre for Cell Imaging (A.D.A., C.V.H., M.R.H.W.), University of Liverpool, Liverpool L69 7ZB, United Kingdom

Address all correspondence and requests for reprints to: Professor Julian Davis, Endocrine Sciences Research Group, School of Clinical & Laboratory Sciences, University of Manchester, Core Technology Facility 3rd floor, 46 Grafton Street, Manchester M13 9NT, United Kingdom. E-mail: julian.davis{at}manchester.ac.uk; or Dr. Antony Adamson, Centre for Cell Imaging, University of Liverpool, Biosciences Building, Crown Street, Liverpool L69 7BZ, United Kingdom. E-mail: a.adamson{at}liv.ac.uk.

Estrogens have been implicated in the regulation of prolactin gene expression in man, although previous studies have not defined the molecular mechanism whereby estradiol activates the human prolactin gene promoter (hPrl). We found that estradiol induced a reproducible 1.8-fold activation of the hPrl gene promoter, using pituitary GH3 cells stably transfected with a 5000-bp hPrl promoter fragment linked to luciferase reporter gene. This activation was blocked by treatment with estrogen receptor (ER) antagonists 4-hydroxytamoxifen and ICI-182,780. Promoter deletion and mutagenesis experiments identified a functional estrogen response element (ERE) sequence 1189 bp upstream of the transcription start site that was responsible for estrogen-mediated promoter activation. This site differed from the consensus ERE sequence by two base pairs, one in each half-site. This ERE was identified to be functional through binding ER in EMSAs. Chromatin immunoprecipitation assays confirmed ER binding to this sequence in vivo in the absence of ligand, with increased recruitment when cells were cultured in the presence of estradiol. When cells were treated with both estradiol and TNF, we observed synergistic activation of the hPrl promoter, which was mediated by the –1189-bp ERE. Mutagenesis of this ERE abolished the promoter-activating effect not only of estradiol but also of TNF. These data suggest a novel, promoter-specific signaling interaction between estrogen and TNF signaling, which is likely to be important for prolactin regulation in vivo.

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