A Mechanism for the Differential Regulation of Gonadotropin Subunit Gene Expression by Gonadotropin-Releasing Hormone

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 92; no. 26; pp. 12280 - 12284
• Main Authors: Kaiser, U B, Sabbagh, E, Katzenellenbogen, R A, Conn, P M, Chin, W W
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences of the United States of America 19-12-1995; National Acad Sciences; National Academy of Sciences
• Subjects: Anatomy & physiology; Animals; Cell Line; Cell lines; Cloning, Molecular; Complementary DNA; Endocrine system; Endocrinology; Follicle Stimulating Hormone - biosynthesis; Gene expression; Gene Expression Regulation; Gonadotropic cells; Gonadotropin-Releasing Hormone - pharmacology; Gonadotropins; Hormones; Luciferases - biosynthesis; Luteinizing Hormone - biosynthesis; Macromolecular Substances; Pituitary Gland; Promoter Regions, Genetic; Rats; Receptors; Receptors, LHRH - biosynthesis; Receptors, LHRH - physiology; Recombinant Proteins - biosynthesis; Recombinant Proteins - metabolism; Reproduction; RNA, Messenger - biosynthesis; Secretion; Sex hormones; Transfection
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.92.26.12280

The hypothalamic hormone gonadotropin-releasing hormone (GnRH) is released in a pulsatile fashion, with its frequency varying throughout the reproductive cycle. Varying pulse frequencies and amplitudes differentially regulate the biosynthesis and secretion of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) by pituitary gonadotropes. The mechanism by which this occurs remains a major question in reproductive physiology. Previous studies have been limited by the lack of available cell lines that express the LH and FSH subunit genes and respond to GnRH. We have overcome this limitation by transfecting the rat pituitary GH3cell line with rat GnRH receptor (GnRHR) cDNA driven by a heterologous promoter. These cells, when cotransfected with regulatory regions of the common α, LHβ, or FSHβ subunit gene fused to a luciferase reporter gene, respond to GnRH with an increase in luciferase activity. Using this model, we demonstrate that different cell surface densities of the GnRHR result in the differential regulation of LH and FSH subunit gene expression by GnRH. This suggests that the differential regulation of gonadotropin subunit gene expression by GnRH observed in vivo in rats may, in turn, be mediated by varying gonadotrope cell surface GnRHR concentrations. This provides a physiologic mechanism by which a single ligand can act through a single receptor to regulate differentially the production of two hormones in the same cell.