TY - JOUR
T1 - Brain-specific expression of novel G-protein-coupled receptors, with homologies to Xenopus PSP24 and human GPR45
AU - Kawasawa, Yuka
AU - Kume, Kazuhiko
AU - Nakade, Shinji
AU - Haga, Hisanori
AU - Izumi, Takashi
AU - Shimizu, Takao
N1 - Funding Information:
We are grateful to Dr. G. Tigyi at University of Tennessee, Memphis, for providing Xenopus PSP24 cDNA. We also thank Dr. D. Wang at the University of Tokyo for comments for the manuscript. This work was supported in part by a Grant-in-Aid from Ministry of Education, Science, Sports, and Culture of Japan.
PY - 2000/10/5
Y1 - 2000/10/5
N2 - 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 PSP24α, β, and human PSP24α, β. The homologies between α and β 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. (C) 2000 Academic Press.
AB - 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 PSP24α, β, and human PSP24α, β. The homologies between α and β 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. (C) 2000 Academic Press.
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U2 - 10.1006/bbrc.2000.3569
DO - 10.1006/bbrc.2000.3569
M3 - Article
C2 - 11027574
AN - SCOPUS:0034609959
SN - 0006-291X
VL - 276
SP - 952
EP - 956
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -