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Molecular cloning and expression of a human anterior pituitary receptor for growth hormone-releasing hormone.
Author(s) -
Bruce D. Gaylinn,
Jeffrey K. Harrison,
John R. Zysk,
Charles E. Lyons,
Kevin R. Lynch,
Michael O. Thorner
Publication year - 1993
Publication title -
molecular endocrinology
Language(s) - English
Resource type - Journals
eISSN - 1944-9917
pISSN - 0888-8809
DOI - 10.1210/mend.7.1.7680413
Subject(s) - biology , complementary dna , secretin , anterior pituitary , receptor , growth hormone releasing hormone receptor , secretin family , vasoactive intestinal peptide , cdna library , endocrinology , medicine , microbiology and biotechnology , hormone receptor , hormone , neuropeptide , gene , biochemistry , secretion , genetics , cancer , breast cancer
GH-releasing hormone (GHRH), acting through the GHRH receptor (GHRH-R), plays a pivotal role in the regulation of GH synthesis and secretion in the pituitary. It is possible that GHRH may serve other roles in other tissues. Here we report the cloning of a cDNA encoding a human GHRH-R from an acromegalic pituitary cDNA library. The isolated cDNA encodes a 423-amino acid protein that has seven putative transmembrane domains characteristic of G-protein-coupled receptors. It is a member of the secretin family of G-protein-coupled receptors and has 47%, 42%, 35%, and 28% identity with receptors for vasoactive intestinal peptide, secretin, calcitonin, and PTH, respectively. Transient expression of this cDNA in COS cells induced saturable, high affinity, GHRH-specific binding and also stimulated intracellular cAMP accumulation in response to physiological concentrations of GHRH. A specific GHRH antagonist blocked both binding and second messenger response. Northern analysis indicated that GHRH-R mRNA was most abundant in extracts of pituitary and was not detected in other tissues.

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