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Transcriptional activation of the membrane‐bound progesterone receptor (mPR) by dioxin, in endocrine‐responsive tissues
Author(s) -
Selmin Ornella,
Thorne Patricia A.,
Blachere Francoise M.,
Johnson Paula D.,
Romagnolo Donato F.
Publication year - 2005
Publication title -
molecular reproduction and development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.745
H-Index - 105
eISSN - 1098-2795
pISSN - 1040-452X
DOI - 10.1002/mrd.20090
Subject(s) - biology , receptor , luciferase , medicine , endocrinology , aryl hydrocarbon receptor , promoter , mediator , ovary , hormone , gene expression , gene , microbiology and biotechnology , biochemistry , transcription factor , transfection
We originally identified the membrane‐bound progesterone receptor (mPR) using a screening for genes differentially expressed in liver of rats exposed to dioxin. Recent findings have suggested a role for the mPR in sperm cells, ovary, and brain; however, its mechanisms of action are largely unknown. In this study, we examined the expression pattern of the mPR in liver of rats exposed to dioxin and identified possible mechanisms of its regulation. We observed that mPR expression was induced by dioxin, but was also dependent on the hormonal responsiveness of the tissue. In particular, in male, but not female liver, dioxin induced the expression of the mPR. However, in control, untreated female liver the level of mPR transcript was higher than in control males. Moreover, in breast cancer cells MCF‐7 dioxin induced mPR expression. Promoter studies using the luciferase assay indicated that a fragment of ∼350 bp of the mPR promoter was able to induce luciferase activity in the presence of dioxin, suggesting that the presumptive XREs sites contained in this mPR promoter region are responsive to dioxin. Analysis of mPR protein level confirmed the results observed at the RNA level, both in rat liver and MCF‐7 cells. Taken together, these observations suggest the existence of a novel cross‐talk between steroid and aromatic hydrocarbon receptors (AhR), and underline the importance of the mPR as a mediator of physiologic effects of the sex hormones. Mol. Reprod. Dev. 70: 166–174, 2005. © 2005 Wiley‐Liss, Inc.