THE BOVINE ALPHA(2D)-ADRENERGIC RECEPTOR GENE - STRUCTURE, EXPRESSIONIN RETINA, AND PHARMACOLOGICAL CHARACTERIZATION OF THE ENCODED RECEPTOR

Citation
V. Venkataraman et al., THE BOVINE ALPHA(2D)-ADRENERGIC RECEPTOR GENE - STRUCTURE, EXPRESSIONIN RETINA, AND PHARMACOLOGICAL CHARACTERIZATION OF THE ENCODED RECEPTOR, Molecular and cellular biochemistry, 177(1-2), 1997, pp. 113-123
Citations number
34
Categorie Soggetti
Biology,"Cell Biology
ISSN journal
03008177
Volume
177
Issue
1-2
Year of publication
1997
Pages
113 - 123
Database
ISI
SICI code
0300-8177(1997)177:1-2<113:TBARG->2.0.ZU;2-#
Abstract
This report describes cloning of the bovine alpha(2D)-adrenergic recep tor (alpha(2D)-AR) gene and determination of the transcription start s ite, unequivocal presence of the alpha(2D)-AR transcript in the retina , and pharmacological characteristics of the encoded product. Furtherm ore, expression of the gene in selected bovine tissues has also been s crutinized. A genomic clone was isolated from lambda EMBL3 Library and a 3 kb fragment was subcloned and sequenced. This fragment contained the putative TATA box and the coding region. The encoded receptor was transiently expressed in COS cells. The recombinant receptor expressed pharmacological characteristics almost identical to the wild-type bov ine retinal receptor, which were typical of the alpha(2D)-AR subtype. RNase protection analysis confirmed the expression of the gene in the retina. The bovine receptor was structurally close to its rat analogue which also encodes the alpha(2D)-AR, but, the highest homology was ob served with the porcine receptor expressing alpha(2A)-AR pharmacologic al characteristics. Certain structural features of the bovine gene wer e unique to itself and not shared by any other alpha(2)-AR subtype. Am ong the tissues tested using reverse transcriptase-polymerase chain re action (RT-PCR), the alpha(2D)-AR message was the most abundant in ret ina, followed by the brain and olfactory lobe. Thus, the availability of the bovine receptor gene probe will become an important additional tool in the elucidation of molecular mechanisms behind the alpha(2D)-A R physiology in neurosensory processes such as those occurring in the eye and the brain.