Expansion of the alpha 2-adrenergic receptor family: cloning and characterization of a human alpha 2-adrenergic receptor subtype, the gene for which is located on chromosome 2
- PMID: 2164221
- PMCID: PMC54268
- DOI: 10.1073/pnas.87.13.5094
Expansion of the alpha 2-adrenergic receptor family: cloning and characterization of a human alpha 2-adrenergic receptor subtype, the gene for which is located on chromosome 2
Abstract
Pharmacologic, biochemical, and genetic analyses have demonstrated the existence of multiple alpha 2-adrenergic receptor (alpha 2AR) subtypes. We have cloned a human alpha 2AR by using the polymerase chain reaction with oligonucleotide primers homologous to conserved regions of the previously cloned alpha 2ARs, the genes for which are located on human chromosomes 4 (C4) and 10 (C10). The deduced amino acid sequence encodes a protein of 450 amino acids whose putative topology is similar to that of the family of guanine nucleotide-binding protein-coupled receptors, but whose structure most closely resembles that of the alpha 2ARs. Competition curve analysis of the binding properties of the receptor expressed in COS-7 cells with a variety of adrenergic ligands demonstrates a unique alpha 2AR pharmacology. Hybridization with somatic cell hybrids shows that the gene for this receptor is located on chromosome 2. Northern blot analysis of various rat tissues shows expression in liver and kidney. The unique pharmacology and tissue localization of this receptor suggest that this is an alpha 2AR subtype not previously identified by classical pharmacological or ligand binding approaches.
Similar articles
-
Molecular cloning and expression of the cDNA for the alpha 1A-adrenergic receptor. The gene for which is located on human chromosome 5.J Biol Chem. 1991 Apr 5;266(10):6365-9. J Biol Chem. 1991. PMID: 1706716
-
Cloning and expression of a human kidney cDNA for an alpha 2-adrenergic receptor subtype.Proc Natl Acad Sci U S A. 1988 Sep;85(17):6301-5. doi: 10.1073/pnas.85.17.6301. Proc Natl Acad Sci U S A. 1988. PMID: 2842764 Free PMC article.
-
Expression of three alpha 2-adrenergic receptor subtypes in rat tissues: implications for alpha 2 receptor classification.Mol Pharmacol. 1990 Nov;38(5):599-603. Mol Pharmacol. 1990. PMID: 2172770
-
Molecular biology of adrenergic receptors: model systems for the study of G-protein-mediated signal transduction.Blood Vessels. 1991;28(1-3):93-103. doi: 10.1159/000158848. Blood Vessels. 1991. PMID: 1848129 Review.
-
Molecular biology of alpha-adrenergic receptors: implications for receptor classification and for structure-function relationships.Biochim Biophys Acta. 1991 Oct 26;1095(2):127-39. doi: 10.1016/0167-4889(91)90075-9. Biochim Biophys Acta. 1991. PMID: 1657194 Review. No abstract available.
Cited by
-
Role of α2-Adrenoceptor Subtypes in Suppression of L-Type Ca2+ Current in Mouse Cardiac Myocytes.Int J Mol Sci. 2021 Apr 16;22(8):4135. doi: 10.3390/ijms22084135. Int J Mol Sci. 2021. PMID: 33923625 Free PMC article.
-
Novel Treatment Targets Based on Insights in the Etiology of Depression: Role of IL-6 Trans-Signaling and Stress-Induced Elevation of Glutamate and ATP.Pharmaceuticals (Basel). 2019 Jul 29;12(3):113. doi: 10.3390/ph12030113. Pharmaceuticals (Basel). 2019. PMID: 31362361 Free PMC article. Review.
-
Guanfacine Extended Release: A New Pharmacological Treatment Option in Europe.Clin Drug Investig. 2016 Jan;36(1):1-25. doi: 10.1007/s40261-015-0336-0. Clin Drug Investig. 2016. PMID: 26585576 Free PMC article. Review.
-
Haplotype polymorphism in the alpha-2B-adrenergic receptor gene influences response inhibition in a large Chinese sample.Neuropsychopharmacology. 2012 Apr;37(5):1115-21. doi: 10.1038/npp.2011.266. Epub 2012 Jan 4. Neuropsychopharmacology. 2012. PMID: 22218095 Free PMC article.
-
Are the pharmacology and physiology of α₂ adrenoceptors determined by α₂-heteroreceptors and autoreceptors respectively?Br J Pharmacol. 2012 Jan;165(1):90-102. doi: 10.1111/j.1476-5381.2011.01533.x. Br J Pharmacol. 2012. PMID: 21658028 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
Associated data
- Actions
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Miscellaneous
