Molecular cloning and expression of the rat beta 1-adrenergic receptor gene
Using the sequence homology approach for cloning related genes within the G-protein-coupled receptor gene family, we have cloned the gene for the rat beta 1-adrenergic receptor (beta 1-AR). The rat beta 1-adrenergic receptor gene was isolated from a lambda EMBL3 rat genomic DNA library using the ham...
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Veröffentlicht in: | The Journal of biological chemistry 1990-08, Vol.265 (22), p.12960-12965 |
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Zusammenfassung: | Using the sequence homology approach for cloning related genes within the G-protein-coupled receptor gene family, we have
cloned the gene for the rat beta 1-adrenergic receptor (beta 1-AR). The rat beta 1-adrenergic receptor gene was isolated from
a lambda EMBL3 rat genomic DNA library using the hamster beta 2-adrenergic receptor (beta 2-AR) coding sequence as a probe
under low stringency hybridization conditions. The rat beta 1-AR gene encodes a protein of 466 amino acids that contains one
consensus site for N-linked glycosylation (Asn-15) and three consensus sites for cAMP-dependent protein kinase phosphorylation
(Ser-296, Ser-301, and Ser-401). The encoded rat beta 1-AR is 98 and 91% similar at the amino acid level with the human beta
1-AR in the transmembrane domains and in the overall sequence, respectively. Genomic Southern blot and gene dosage analyses
indicate that the rat beta 1-AR gene is a single copy gene. The tissue distribution of the rat beta 1-AR mRNA was highest
in the pineal gland with other brain regions and peripheral tissues, including the heart, expressing the mRNA at moderate
levels. The bacteriophage clone containing the rat beta 1-AR gene with its natural promoter was co-transfected with the selectable
marker (pRSVneo) conferring neomycin resistance into beta 1-AR-deficient mouse L cells. Analyses of the selected transfectant
demonstrates efficient expression of the beta 1-AR gene and functional receptor. 125I-Labeled iodocyanopindolol bound transfectant
membranes with an affinity of KD = 24 pm; the beta 1-AR-selective antagonist ICI 89,406 displaced iodocyanopindolol binding
with a Ki approximately 140 times lower than that for the beta 2-AR-selective antagonist ICI 118,551. In addition, in the
transfectant cell line, adenylylcyclase was stimulated by beta-adrenergic receptor agonists with the rank order of potency
of isoproterenol greater than norepinephrine = epinephrine, consistent with properties expected of the beta 1-AR subtype. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1016/S0021-9258(19)38253-5 |