THE CLONING AND CHROMOSOMAL MAPPING OF 2 NOVEL HUMAN OPIOID-SOMATOSTATIN-LIKE RECEPTOR GENES, GPR7 AND GPR8, EXPRESSED IN DISCRETE AREAS OF THE BRAIN

被引:106
作者
ODOWD, BF
SCHEIDELER, MA
NGUYEN, T
CHENG, R
RASMUSSEN, JS
MARCHESE, A
ZASTAWNY, R
HENG, HHQ
TSUI, LC
SHI, XM
ASA, S
PUY, L
GEORGE, SR
机构
[1] ADDICT RES FDN,TORONTO,ON M5S 2S1,CANADA
[2] UNIV TORONTO,DEPT PHARMACOL,TORONTO,ON M5S 1A8,CANADA
[3] UNIV TORONTO,DEPT MED,TORONTO,ON M5S 1A8,CANADA
[4] NOVO NORDISK AS,DK-2760 MOLOV PARK,DENMARK
[5] HOSP SICK CHILDREN,RES INST,DEPT GENET,TORONTO,ON M5G 1X8,CANADA
[6] MT SINAI HOSP,DEPT PATHOL,TORONTO,ON M5G 1X5,CANADA
关键词
D O I
10.1006/geno.1995.1109
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Following the cloning of the opioid receptors mu, kappa, and delta, we conducted a search for related receptors. Using oligonucleotides based on the opioid and also the structurally related somatostatin receptors, we amplified genomic DNA using the polymerase chain reaction and isolated fragments of novel Gr protein-coupled receptor genes. Two of these gene fragments designated clones 12 and 11 were used to isolate the full-length genes, The intronless coding sequences of these genes, named GPR7 and GPR8, shared 70% identity with each other, and each shared significant similarity with the sequences encoding transmembrane regions of the opioid and somatostatin receptors. GPR7 was mapped to chromosome 10q11.2-q21.1 and GPR8 to chromosome 20q13.3. Northern blot analysis using human mRNA demonstrated expression of GPR7 mainly in cerebellum and frontal cortex, while GPR8 was located mainly in the frontal cortex. In situ hybridization revealed expression of GPR7 in the human pituitary, A partial sequence of the mouse orthologue of GPR7 was obtained, and in situ hybridization demonstrated expression in discrete nuclei of brain, namely suprachiasmatic, arcuate, and ventromedial nuclei of hypothalamus. A stable cell line expressing the GPR7 gene was created, but expression levels of the receptor were low. The available pharmacology indicated binding to several opioid drugs such as bremazocine, levorphanol, and beta-FNA, but not to the opioid receptor subtype-selective mu, delta, or kappa agonists. (C) 1995 Academic Press,Inc.
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页码:84 / 91
页数:8
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