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HPMR

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Growth Hormone-releasing Hormone Receptor OKDB#: 47
 Symbols: GHRHR Species: human
 Synonyms: GROWTH HORMONE-RELEASING FACTOR RECEPTOR, GHRFR|  Locus: 7p15-p14 in Homo sapiens
HPMR


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General Comment Growth hormone-releasing hormone (GHRH), acting through the GHRH receptor, plays a pivotal role in the regulation of GH synthesis and secretion in the pituitary. Gaylinn et al. (1993) cloned a cDNA encoding the human GHRH receptor from an acromegalic pituitary cDNA library. The isolated cDNA predicted a 423-amino acid protein that has 7 transmembrane domains characteristic of G protein-coupled receptors. It is a member of the secretin family of G protein-coupled receptors and has significant homology with receptors for vasoactive intestinal peptide, secretin, calcitonin, and parathyroid hormone.

NCBI Summary: Growth hormone releasing hormone receptor; may act through increasing intracellular cAMP levels; member of the G protein-coupled receptor family
General function Receptor
Comment
Cellular localization Plasma membrane
Comment
Ovarian function Ovulation, Steroid metabolism
Comment The hypothalamic neuropeptide, GHRH, is formed in the ovary and acts via specific receptors in granulosa cells to enhance cAMP production and steroidogenic responses to the pituitary gonadotropins. Karakji et al. (1995) demonstrated that GHRH treatment stimulates rat granulosa cell plasminogen activator activity in vitro.
Expression regulated by FSH
Comment Expression of GHRH binding sites was measured with radioiodinated His1, Nle27]human GRF(1-32)NH2 in cultured granulosa cells [(Bagnato et al., 1991). Treatment with FSH promotes the expression of GHRH receptors in granulosa cells through cAMP-dependent mechanisms.
Ovarian localization Granulosa
Comment
Follicle stages Antral
Comment
Phenotypes
Mutations 2 mutations

Species: human
Mutation name: None
type: naturally occurring
fertility: subfertile
Comment: Wajnrajch et al. (1996) demonstrated a nonsense mutation in the human GHRHR gene. The phenotype in this Indian Moslem kindred was comparable to that in the 'little' mouse.

Species: mouse
Mutation name: Little
type: naturally occurring
fertility: subfertile
Comment: Lin et al. (1993) demonstrated that the molecular basis for the 'little' (lit) mouse phenotype, characterized by a hypoplastic anterior pituitary gland, is a point mutation in the growth hormone releasing factor receptor.

Genomic Region show genomic region
Phenotypes and GWAS show phenotypes and GWAS
Links
OMIM (Online Mendelian Inheritance in Man: an excellent source of general gene description and genetic information.)
OMIM \ Animal Model
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created: July 22, 1999, midnight by: Hsueh   email:
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last update: Aug. 8, 2001, 2:56 p.m. by: Hsueh    email:



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