Chronic Hypersecretion of Luteinizing Hormone in Transgenic Mice Selectively Alters Responsiveness of the α-Subunit Gene to Gonadotropin-Releasing Hormone and Estrogens

• Published in: Molecular endocrinology (Baltimore, Md.) Vol. 13; no. 9; pp. 1449 - 1459
• Main Authors: Abbud, Rula A, Ameduri, Rebecca K, Rao, J. Sunil, Nett, Terry M, Nilson, John H
• Format: Journal Article
• Language: English
• Published: United States Endocrine Society 01.09.1999
• Subjects: Animals; Cattle; Dihydrotestosterone - pharmacology; Dihydrotestosterone - therapeutic use; Estrogen Replacement Therapy; Estrogens - pharmacology; Estrogens - therapeutic use; Female; Gene Expression Regulation - drug effects; Gene Expression Regulation, Developmental; Gonadotropin-Releasing Hormone - pharmacology; Gonadotropin-Releasing Hormone - therapeutic use; Gonadotropins - genetics; Luteinizing Hormone - blood; Luteinizing Hormone - genetics; Luteinizing Hormone - secretion; Mice; Mice, Transgenic; Ovariectomy; Pituitary Gland - metabolism; Promoter Regions, Genetic; RNA, Messenger - metabolism; Time Factors; Trans-Activators - genetics
• ISSN: 0888-8809; 1944-9917
• DOI: 10.1210/mend.13.9.0348

Steroid hormones can act either at the level of the hypothalamus or the pituitary to regulate gonadotropin subunit gene expression. However, their exact site of action remains controversial. Using the bovine gonadotropin α-subunit promoter linked to an expression cassette encoding the β-subunit of LH, we have developed a transgenic mouse model where hypersecretion of LH occurs despite the presence of elevated ovarian steroids. We used this model to determine how hypersecretion of LH could occur when steroid levels are pathological. During transition from the neonatal period to adulthood, the endogenous LHβ subunit gene becomes completely silent in these mice, whereas the α-directed transgene and endogenous α-subunit gene remain active. Interestingly, gonadectomy stimulates expression of the endogenous α and LHβ subunit genes as well as the transgene; however, only the endogenous LHβ gene retains responsiveness to 17β-estradiol and GnRH. In contrast, LH levels remain responsive to negative regulation by androgen. Thus, α-subunit gene expression, as reflected by both the transgene and the endogenous gene, has become independent of GnRH regulation and, as a result, unresponsive to estradiol-negative feedback. This process is accompanied by a decrease in estrogen receptor α gene expression as well as an increase in the expression of transcription factors known to regulate the α-subunit promoter, such as cJun and P-LIM. These studies provide in vivo evidence that estrogen-negative feedback on α and LHβ subunit gene expression requires GnRH input, reflecting an indirect mechanism of action of the steroid. In contrast, androgen suppressesα -subunit expression in both transgenic and nontransgenic mice. This suggests that androgens must regulate α-subunit promoter activity independently of GnRH. In addition to allowing the assessment of site of action of sex steroids on α-subunit gene expression, these studies also indicate that chronic exposure of the pituitary to LH-dependent ovarian hyperstimulation leads to a heretofore-undescribed pathological condition, whereby normal regulation of α, but not LHβ, subunit gene expression becomes compromised.