Androgen suppression of GnRH-stimulated rat LHbeta gene transcription occurs through Sp1 sites in the distal GnRH-responsive promoter region
| Autor: | Nicole Farmer, Shannon C. Jenkins, Daniel J. Haisenleder, Alice C. Anderson, Margaret A. Shupnik, Denis Curtin, Elizabeth M. Wilson, Emilie F. Rissman |
|---|---|
| Rok vydání: | 2001 |
| Předmět: |
Steroidogenic factor 1
Male endocrine system medicine.medical_specialty Transcription Genetic medicine.drug_class Sp1 Transcription Factor Transgene Response element Mice Transgenic Biology Gonadotropic cell Response Elements Steroidogenic Factor 1 Transfection Gonadotropin-Releasing Hormone Mice Endocrinology Suppression Genetic Transcription (biology) Internal medicine medicine Animals Promoter Regions Genetic Molecular Biology Cells Cultured Binding Sites Promoter Dihydrotestosterone General Medicine Luteinizing Hormone Androgen Rats Glycoprotein Hormones alpha Subunit Receptors Androgen Pituitary Gland Female hormones hormone substitutes and hormone antagonists Receptors LHRH medicine.drug |
| Zdroj: | Molecular endocrinology (Baltimore, Md.). 15(11) |
| ISSN: | 0888-8809 |
| Popis: | Steroids may regulate LH subunit gene transcription by modulating hypothalamic GnRH pulse patterns or by acting at the pituitary gonadotrope to alter promoter activity. We tested direct pituitary effects of the androgen dihydrotestosterone (DHT) to modulate the rat LHbeta promoter in transfected LbetaT2 clonal gonadotrope cells and in pituitaries of transgenic mice expressing LHbeta-luciferase. The LHbeta promoter (-617 to +44 bp)-luciferase construct was stimulated in LbetaT2 cells 7- to 10-fold by GnRH. Androgen treatment had little effect on basal promoter activity but suppressed GnRH stimulation by approximately 75%. GnRH stimulation of LHbeta was also suppressed by DHT in isolated pituitary cells from male or female mice with functional nuclear ARs, but not in male littermates with mutant AR. GnRH stimulation of the LHbeta promoter requires interactions between a complex distal response element containing two specificity protein-1 (Sp1) binding sites and a CArG box, and a proximal element with two bipartite binding sites for steroidogenic factor-1 and early growth response protein-1 (Egr-1). DHT effectively suppressed promoter constructs with an intact distal response element. The distal response element does not bind AR, but AR reduces Sp1 binding to this region. Glutathione-S-transferase pull-down studies demonstrated direct interactions of AR with Sp1, which requires the DNA-binding domain of AR, and weaker interactions with Egr-1. We conclude that androgen suppression of the rat LHbeta promoter occurs primarily through direct interaction of AR with Sp1, with some possible role through binding to Egr-1. These interactions result in interference with GnRH-stimulated gene transcription by reducing cooperation between the distal and proximal GnRH response elements. |
| Databáze: | OpenAIRE |
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