Kawasawa Y, Kume K, Nakade S, Haga H, Izumi T, Shimizu T
Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of Tokyo, Bunkyo-ku, Tokyo, 113-0033, Japan.
Biochem Biophys Res Commun. 2000 Oct 5;276(3):952-6. doi: 10.1006/bbrc.2000.3569.
From mouse genomic libraries and human brain cDNA, we cloned three novel G-protein-coupled receptors (GPCRs), which have about 55-70% homologies with Xenopus PSP24 (xPSP24). Together with another human cDNA (GPR45) cloned by Marchese et al. (Genomics 56, 12-21, 1999). they comprise a family of mammalian PSP24s. Therefore, we termed these clones mouse PSP24alpha, beta, and human PSP24alpha, beta. The homologies between alpha and beta isoforms were 54% for human and 51% for mouse clones. None of these clones shares sequence similarities with any known mammalian GPCRs, thus forming a unique gene family. Northern blot demonstrated that both of the mouse transcripts were predominantly expressed in the brain. In situ hybridization of brain sections showed that the expression was observed in neuronal cells, such as olfactory mitral cells, cortical neurons, hippocampal pyramidal cells, and Purkinje cells in the cerebellum. We suggest that mammalian PSP24 is a distinct GPCR family and plays a role in the brain function.
从小鼠基因组文库和人类大脑cDNA中,我们克隆了三种新型G蛋白偶联受体(GPCR),它们与非洲爪蟾PSP24(xPSP24)具有约55 - 70%的同源性。与Marchese等人克隆的另一种人类cDNA(GPR45)(《基因组学》56卷,第12 - 21页,1999年)一起,它们构成了一个哺乳动物PSP24家族。因此,我们将这些克隆分别命名为小鼠PSP24α、β以及人类PSP24α、β。人类α和β亚型之间的同源性为54%,小鼠克隆的同源性为51%。这些克隆与任何已知的哺乳动物GPCR均无序列相似性,从而形成了一个独特的基因家族。Northern印迹法表明,两种小鼠转录本主要在大脑中表达。脑切片的原位杂交显示,在神经元细胞中观察到了表达,如嗅球的二尖瓣细胞、皮质神经元、海马锥体细胞以及小脑的浦肯野细胞。我们认为哺乳动物PSP24是一个独特的GPCR家族,在脑功能中发挥作用。