CLONING AND CHROMOSOMAL MAPPING OF 3 NOVEL GENES, GPR9, GPR10, AND GPR14 ENCODING RECEPTORS RELATED TO INTERLEUKIN-8, NEUROPEPTIDE-Y, AND SOMATOSTATIN RECEPTORS

被引:170
作者
MARCHESE, A
HEIBER, M
NGUYEN, T
HENG, HHQ
SALDIVIA, VR
CHENG, R
MURPHY, PM
TSUI, LC
SHI, XM
GREGOR, P
GEORGE, SR
ODOWD, BF
DOCHERTY, JM
机构
[1] UNIV TORONTO,DEPT PHARMACOL,TORONTO,ON M5S 1A8,CANADA
[2] UNIV TORONTO,DEPT MED,TORONTO,ON M5S 1A8,CANADA
[3] ADDICT RES FDN,TORONTO,ON M5S 2S1,CANADA
[4] NIAID,DEPT HLTH & HUMAN SERV,HOST DEF LAB,BETHESDA,MD 20892
[5] HOSP SICK CHILDREN,RES INST,DEPT GENET,TORONTO,ON M5G 1X8,CANADA
[6] BAYER,W HAVEN,CT 06516
关键词
D O I
10.1006/geno.1995.9996
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
We employed the polymerase chain reaction and genomic DNA library screening to clone novel human genes, GPR9 and GPR10, and a rat gene, GPR14. GPR9, GPR10, and GPR14 each encode G protein-coupled receptors. GPR10 and GPR14 are intronless within their coding regions, while GPR9 contains at least one intron. The receptor encoded by GPR9 shares the highest identity with human IL-8 receptor type B (38% overall and 53% in the transmembrane regions), followed by IL-8 receptor type A (36% overall and 51% in the transmembrane domains). GPR10 encodes a receptor that shares highest identity with the neuropeptide Y receptor (31% overall and 46% in the transmembrane domains). The receptor encoded by GPR14 shares highest identity with the somatostatin receptor SSTR 4 (27% overall and 41% in the transmembrane domains). Fluorescence in situ hybridization analysis localized GPR9 to chromosome 8p11.2-p12 and GPR10 to chromosome 10q25.3-q26. (C) 1995 Academic Press, Inc.
引用
收藏
页码:335 / 344
页数:10
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