Marchese A, Docherty J M, Nguyen T, Heiber M, Cheng R, Heng H H, Tsui L C, Shi X, George S R, O'Dowd B F
Addiction Research Foundation, Toronto, Ontario, Canada.
Genomics. 1994 Oct;23(3):609-18. doi: 10.1006/geno.1994.1549.
We report the isolation and characterization of several novel human genes encoding G protein-coupled receptors. Each of the receptors contained the familiar seven transmembrane topography and most closely resembled peptide binding receptors. Gene GPR1 encoded a receptor protein that is intronless in the coding region and that shared identity (43% in the transmembrane regions) with the opioid receptors. Northern blot analysis revealed that GPR1 transcripts were expressed in the human hippocampus, and the gene was localized to chromosome 15q21.6. Gene GPR2 encoded a protein that most closely resembled an interleukin-8 receptor (51% in the transmembrane regions), and this gene, not expressed in the six brain regions examined, was localized to chromosome 17q21.1-q21.3. A third gene, GPR3, showed identity (56% in the transmembrane regions) with a previously characterized cDNA clone from rat and was localized to chromosome 1p35-p36.1.
我们报告了几个编码G蛋白偶联受体的新型人类基因的分离和特性鉴定。每个受体都具有常见的七跨膜结构,并且与肽结合受体最为相似。基因GPR1编码一种受体蛋白,其编码区无内含子,并且与阿片受体具有同源性(跨膜区为43%)。Northern印迹分析显示,GPR1转录本在人类海马体中表达,该基因定位于染色体15q21.6。基因GPR2编码一种与白细胞介素-8受体最为相似的蛋白(跨膜区为51%),该基因在所检测的六个脑区中均未表达,定位于染色体17q21.1-q21.3。第三个基因GPR3与先前鉴定的大鼠cDNA克隆具有同源性(跨膜区为56%),定位于染色体1p35-p36.1。