The proximal promoter of the bovine luteinizing hormone beta-subunit gene confers gonadotrope-specific expression and regulation by gonadotropin-releasing hormone, testosterone, and 17 beta-estradiol in transgenic mice
| Autor: | J Gorski, M.W. Wolfe, J Yeung, T L Saunders, Sally A. Camper, Thomas E. Wagner, Terry M. Nett, S K Kendall, I Anderson, Ruth A. Keri |
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| Rok vydání: | 1994 |
| Předmět: |
Chloramphenicol O-Acetyltransferase
Male endocrine system medicine.medical_specialty medicine.drug_class Ovariectomy Transgene Molecular Sequence Data Estrogen receptor Mice Transgenic Gonadotropin-releasing hormone Biology Transfection Gonadotropic cell Gonadotropin-releasing hormone antagonist Gonadotropin-Releasing Hormone Mice Endocrinology Internal medicine medicine Animals Testosterone Promoter Regions Genetic Beta (finance) Molecular Biology Regulation of gene expression Base Sequence Estradiol General Medicine Luteinizing Hormone Gene Expression Regulation Pituitary Gland Cattle Female Luteinizing hormone Oligopeptides Orchiectomy |
| Zdroj: | Molecular Endocrinology. 8:1807-1816 |
| ISSN: | 1944-9917 0888-8809 |
| DOI: | 10.1210/mend.8.12.7708066 |
| Popis: | Transient transfection studies have proven useful in unraveling the molecular mechanisms underlying gonadotrope-specific expression and hormonal regulation of the gene encoding the alpha-subunit of the glycoprotein hormones. In contrast, similar studies performed with the LH beta gene have been less informative. When assayed by transient transfection into alpha T3-1 cells, activity of a 776-basepair bovine LH beta promoter-chloramphenicol acetyltransferase fusion gene (bLH beta CAT) was no greater than that of a promoterless control. To determine whether limited activity in vitro reflected the absence of critical regulatory elements, we examined activity of bovine LH beta fusion genes after stable integration in transgenic mice. In contrast to transient transfection studies, the LH beta promoter targeted high levels of CAT expression specifically to the pituitary. In addition, a bLH beta TK fusion gene was active only in gonadotropes. The bLH beta CAT transgene was also evaluated for responsiveness to gonadal steroids and GnRH. Testosterone and 17 beta-estradiol were capable of suppressing activity 70-80% in castrated males, despite the absence of high affinity binding sites for androgen or estrogen receptors. This suggests that feedback inhibition of LH beta CAT transgene expression by gonadal steroids may occur through an indirect mechanism, possibly at the level of the hypothalamus. To address whether the bLH beta CAT transgene could be regulated by GnRH, we treated ovariectomized females with antide, a GnRH antagonist. Antide suppressed transgene activity by 60%. Thus, the proximal promoter of the bovine LH beta subunit gene directs appropriate patterns of cell-specific expression and retains responsiveness to gonadal steroids and GnRH. In light of the robust activity of the LH beta promoter in transgenic mice, we suggest that this animal model can be exploited further to dissect the complex mechanisms that underlie gonadotrope-specific expression and hormonal regulation of the LH beta gene. |
| Databáze: | OpenAIRE |
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