Y-receptor-like genes GPR72 and GPR73: molecular cloning, genomic organisation and assignment to human chromosome 11q21.1 and 2p14 and mouse chromosome 9 and 6

被引:31
作者
Parker, R
Liu, M
Eyre, HJ
Copeland, NG
Gilbert, DJ
Crawford, J
Sutherland, GR
Jenkins, NA
Herzog, H
机构
[1] St Vincents Hosp, Garvan Inst Med Res, Neurobiol Program, Sydney, NSW 2010, Australia
[2] Womens & Childrens Hosp, Dept Cytogenet & Mol Genet, Ctr Med Genet, Adelaide, SA 5006, Australia
[3] Frederick Canc Res & Dev Ctr, Mammalian Genet Lab, ABL Basic Res Program, Frederick, MD 21702 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 2000年 / 1491卷 / 1-3期
基金
英国医学研究理事会;
关键词
G-protein coupled receptor; neuropeptide Y; ligand binding; cell-surface expression;
D O I
10.1016/S0167-4781(00)00023-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two novel G-protein-coupled receptors, one from human, GPR72, and one from mouse, GPR73 have been isolated, sequenced and their genomic organisation determined. Non-isotopic in situ hybridisation and radiation hybrid mapping have identified GPR72 to be localised on human chromosome 11q21.1, and GPR73 on human chromosome 2p14. Interspecific mouse backcross mapping has localised the genes to mouse chromosomes 9 and 6, respectively. Northern analysis reveals GPR72 mRNA expression only in brain tissue. However, GPR73 mRNA can be found in heart, skeletal muscle and pancreas. Both receptors are closely related with 36 and 33% overall amino acid identity, respectively, to the Y-receptor family. However, although successful cell surface expression in a heterologous expression system can be achieved no specific binding to this ligand family can be detected, indicating that perhaps additional factors are required for binding. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:369 / 375
页数:7
相关论文
共 18 条
[1]  
ADAMS MD, 1995, NATURE, V377, P3
[2]   Real-time optical monitoring of ligand-mediated internalization of α1b-adrenoceptor with green fluorescent protein [J].
Awaji, T ;
Hirasawa, A ;
Kataoka, M ;
Shinoura, H ;
Nakayama, Y ;
Sugawara, T ;
Izumi, S ;
Tsujimoto, G .
MOLECULAR ENDOCRINOLOGY, 1998, 12 (08) :1099-1111
[3]   Y-receptor subtypes - How many more? [J].
Blomqvist, AG ;
Herzog, H .
TRENDS IN NEUROSCIENCES, 1997, 20 (07) :294-298
[4]  
BREATHNACH R, 1981, ANNU REV BIOCHEM, V50, P349, DOI 10.1146/annurev.bi.50.070181.002025
[5]  
CALLEN DF, 1990, ANN GENET-PARIS, V33, P219
[6]   DEVELOPMENT AND APPLICATIONS OF A MOLECULAR GENETIC-LINKAGE MAP OF THE MOUSE GENOME [J].
COPELAND, NG ;
JENKINS, NA .
TRENDS IN GENETICS, 1991, 7 (04) :113-118
[7]  
EDELHOFF S, 1994, ONCOGENE, V9, P665
[8]   Characterization of Y-3 receptor-mediated synaptic inhibition by chimeric neuropeptide Y-peptide YY peptides in the rat brainstem [J].
Glaum, SR ;
Miller, RJ ;
Rhim, H ;
Maclean, D ;
Georgic, LM ;
MacKenzie, RG ;
Grundemar, L .
BRITISH JOURNAL OF PHARMACOLOGY, 1997, 120 (03) :481-487
[9]   IDENTIFICATION OF A GENE INDUCED BY GLUCOCORTICOIDS IN MURINE T-CELLS - A POTENTIAL-G PROTEIN-COUPLED RECEPTOR [J].
HARRIGAN, MT ;
CAMPBELL, NF ;
BOURGEOIS, S .
MOLECULAR ENDOCRINOLOGY, 1991, 5 (09) :1331-1338
[10]  
HERZOG H, 1992, P NATL ACAD SCI USA, V88, P10931