Bräuner-Osborne H, Krogsgaard-Larsen P
NeuroScience PharmaBiotec Research Centre, Department of Medical Chemistry, The Royal Danish School of Pharmacy, 2 Universitetsparken, Copenhagen, DK-2100, Denmark.
Genomics. 2000 Apr 15;65(2):121-8. doi: 10.1006/geno.2000.6164.
Query of GenBank with the amino acid sequence of human metabotropic glutamate receptor subtype 2 (mGluR2) identified a predicted gene product of unknown function on BAC clone CIT987SK-A-69G12 (located on chromosome band 16p12) as a homologous protein. The transcript, entitled GPRC5B, was cloned from an expressed sequence tag clone that contained the entire open reading frame of the transcript encoding a protein of 395 amino acids. Analysis of the protein sequence reveal that GPRC5B contains a signal peptide and seven transmembrane alpha-helices, which is a hallmark of G-protein-coupled receptors (GPCRs). GPRC5B displays homology to retinoic acid-inducible gene 1 (RAIG1, 33% sequence identity) and to several family C (mGluR-like) GPCRs (20-25% sequence identity). Both RAIG1 and GPRC5B have short extracellular amino-terminal domains (ATDs) that contrast the very long ATDs characterizing the receptors currently assigned to family C. However, our results strongly indicate that RAIG1 and GPRC5B form a new subgroup of family C characterized by short ATDs. GPRC5B mRNA is widely expressed in peripheral and central tissues with highest abundance in kidney, pancreas, and testis. This mRNA expression pattern is markedly different from that of RAIG1, which shows a slightly more restricted expression pattern with highest abundance in lung tissue.
用人代谢型谷氨酸受体2型(mGluR2)的氨基酸序列查询GenBank,在BAC克隆CIT987SK - A - 69G12(位于染色体带16p12)上鉴定出一个功能未知的预测基因产物作为同源蛋白。该转录本名为GPRC5B,是从一个表达序列标签克隆中克隆出来的,该克隆包含编码395个氨基酸蛋白质的转录本的完整开放阅读框。对蛋白质序列的分析表明,GPRC5B包含一个信号肽和七个跨膜α螺旋,这是G蛋白偶联受体(GPCRs)的标志。GPRC5B与视黄酸诱导基因1(RAIG1,序列同一性为33%)以及几个C家族(类mGluR)GPCRs(序列同一性为20 - 25%)显示出同源性。RAIG1和GPRC5B都有短的细胞外氨基末端结构域(ATDs),这与目前归为C家族的受体所具有的非常长的ATDs形成对比。然而,我们的结果强烈表明,RAIG1和GPRC5B形成了一个以短ATDs为特征的C家族新亚组。GPRC5B mRNA在周围组织和中枢组织中广泛表达,在肾脏、胰腺和睾丸中丰度最高。这种mRNA表达模式与RAIG1明显不同,RAIG1的表达模式略显受限,在肺组织中丰度最高。