Matsuo Ayako, Matsumoto Shun-ichiro, Nagano Mamoru, Masumoto Koh-hei, Takasaki Jun, Matsumoto Mitsuyuki, Kobori Masato, Katoh Masao, Shigeyoshi Yasufumi
Department of Anatomy and Neurobiology, Kinki University School of Medicine, Osaka-Sayama, Osaka 589-8511, Japan.
Biochem Biophys Res Commun. 2005 May 27;331(1):363-9. doi: 10.1016/j.bbrc.2005.03.174.
G-protein-coupled receptors (GPCRs) are important mediators of signal transduction and are therefore potential targets for pharmacological therapeutics. Here, we report the identification and characterization of an orphan GPCR, termed GPRg1, which was found in the GenBank database following searches with GPCR query sequences. Quantitative PCR analysis revealed that GPRg1 transcripts are expressed almost exclusively in the brain. Moreover, in situ hybridization experiments in brain demonstrated that GPRg1 is abundantly expressed in the ventrolateral region of caudate putamen, the habenular nucleus, the zona incerta, and the medial mammillary nucleus. In addition, overexpression of GPRg1 in 293-EBNA cells activates serum response factor mediated transcription, which was completely inhibited by the Gq/11 selective inhibitor YM-254890, indicating the coupling of GPRg1 with Gq/11. These findings suggest that GPRg1 is a candidate receptor for novel physiologically bioactive substrates and that it plays important roles in the central nervous system.
G蛋白偶联受体(GPCRs)是信号转导的重要介质,因此是药物治疗的潜在靶点。在此,我们报告了一种孤儿GPCR(称为GPRg1)的鉴定和表征,它是在用GPCR查询序列进行搜索后在GenBank数据库中发现的。定量PCR分析表明,GPRg1转录本几乎只在大脑中表达。此外,大脑中的原位杂交实验表明,GPRg1在尾状壳核的腹外侧区域、缰核、未定带和乳头体内侧核中大量表达。此外,GPRg1在293-EBNA细胞中的过表达激活了血清反应因子介导的转录,而Gq/11选择性抑制剂YM-254890完全抑制了这种转录,这表明GPRg1与Gq/11偶联。这些发现表明,GPRg1是新型生理活性底物的候选受体,并且在中枢神经系统中发挥重要作用。