Polymorphisms of Adrenergic Receptors: Variations on a Theme
- 1 April 2003
- journal article
- review article
- Published by Mary Ann Liebert Inc in ASSAY and Drug Development Technologies
- Vol. 1 (2) , 317-326
- https://doi.org/10.1089/15406580360545134
Abstract
Recent studies have revealed that most of the adrenergic receptor genes are polymorphic, leading to changes in the amino sequence of the encoded receptor. The variations occur in multiple functional regions of the receptors, and appear as haplotypes with other coding and noncoding polymorphisms in their genes. The consequences of such genetic variability have been explored in recombinant cell-based systems and in human studies. Adrenergic receptor polymorphisms have been shown to alter receptor binding, G-protein coupling, regulation, and expression compared with their allelic counterparts. Here, the genetic and molecular characterization of these polymorphisms is reviewed, as well as their potential impact on pharmacogenetics, disease risk, and disease modification.Keywords
This publication has 33 references indexed in Scilit:
- Pharmacology and Physiology of Human Adrenergic Receptor polymorphismsAnnual Review of Pharmacology and Toxicology, 2003
- Polymorphisms of the β2-Adrenergic ReceptorNew England Journal of Medicine, 2002
- Amino Acid 49 Polymorphisms of the Human β 1 -Adrenergic Receptor Affect Agonist-Promoted TraffickingJournal of Cardiovascular Pharmacology, 2002
- Genetic Variations and Polymorphisms of G Protein-Coupled Receptors: Functional and Therapeutic ImplicationsAnnual Review of Pharmacology and Toxicology, 2001
- A Four Amino Acid Deletion Polymorphism in the Third Intracellular Loop of the Human α2C-Adrenergic Receptor Confers Impaired Coupling to Multiple EffectorsPublished by Elsevier ,2000
- The Ile164 beta2-adrenergic receptor polymorphism adversely affects the outcome of congestive heart failure.Journal of Clinical Investigation, 1998
- Pharmacological characterization of a recently described human beta 3- adrenergic receptor mutantEndocrinology, 1996
- Chimeric Mutagenesis of Putative G-protein Coupling Domains of the α2A-Adrenergic ReceptorPublished by Elsevier ,1996
- Four Consecutive Serines in the Third Intracellular Loop Are the Sites for β-Adrenergic Receptor Kinase-mediated Phosphorylation and Desensitization of the α2A-Adrenergic ReceptorPublished by Elsevier ,1995