PUBLICATION

Identification of the Endogenous Ligands for Chicken Growth Hormone-releasing Hormone (GHRH) Receptor: Evidence for a Separate Gene Encoding GHRH in Submammalian Vertebrates

Authors
Wang, Y., Li, J., Ying Wang, C., Ho Yan Kwok, A., and Leung, F.C.
ID
ZDB-PUB-070212-25
Date
2007
Source
Endocrinology   148(5): 2405-2416 (Journal)
Registered Authors
Keywords
Chicken, GHRH, GHRH-like peptide, GHRHR, PACAP
MeSH Terms
  • Amino Acid Sequence
  • Animals
  • Brain/physiology*
  • CHO Cells
  • Chickens/genetics*
  • Chickens/metabolism
  • Cloning, Molecular
  • Cricetinae
  • Cricetulus
  • Culture Media, Conditioned/pharmacology
  • DNA, Complementary
  • Evolution, Molecular
  • Gene Expression
  • Growth Hormone-Releasing Hormone/genetics*
  • Growth Hormone-Releasing Hormone/metabolism*
  • Ligands
  • Molecular Sequence Data
  • Peptide Fragments/metabolism
  • Pituitary Adenylate Cyclase-Activating Polypeptide/genetics
  • Pituitary Adenylate Cyclase-Activating Polypeptide/metabolism
  • RNA, Messenger
  • Receptors, Neuropeptide/metabolism*
  • Receptors, Pituitary Hormone-Regulating Hormone/metabolism*
  • Species Specificity
  • Vertebrates
PubMed
17272401 Full text @ Endocrinology
Abstract
It is generally believed that hypothalamic GHRH activates growth hormone-releasing hormone receptor (GHRHR) to stimulate growth hormone synthesis and release in the pituitary of mammals. However, the identity of the endogenous ligand of GHRHR is still unresolved in submammalian vertebrates including birds. In this study, we have successfully identified the chicken GHRH (cGHRH) gene, which consists of 7 exons including two exons (exons 4 and 5) coding for the predicted mature GHRH peptide of 47 amino acids. Interestingly, the differential usage of splice donor sites at exon 6 results in the generation of two prepro-GHRHs (172 a.a. and 188 a.a. in length) with different C-terminal tails. Similar to mammals, cGHRH was detected to be predominantly expressed in the hypothalamus by RT-PCR assay. Using the pGL3-CRE-luciferase reporter system, we further demonstrated that both the synthetic cGHRH peptides (cGHRH1-47 and cGHRH1-31) and conditioned medium from CHO cells expressing cGHRH could strongly induce luciferase activity via activation of cGHRHR, indicating that cGHRH could bind cGHRHR and activate downstream cAMP-PKA signaling pathway. Using the same system, cGHRH-like peptide was also shown to be capable of activating cGHRHR in vitro. As in chicken, a conserved GHRH gene was identified in the genomes of lower vertebrate species including zebrafish, fugu, tetraodon, and Xenopus by synteny analysis. Collectively, our data suggest that GHRH, perhaps together with GHRH-like peptide (chicken/carp-like), may function as the authentic endogenous ligands of GHRHR in chicken as well as in other lower vertebrate species.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping