Characterization of Gpr101 expression and G-protein coupling selectivity

被引:44
作者
Bates, Brian
Zhang, Lynn
Nawoschik, Stan
Kodangattil, Sreekumar
Tseng, Eugene
Kopsco, David
Kramer, Angela
Shan, Qin
Taylor, Noel
Johnson, Jeremy
Sun, Ying
Chen, Hui Min
Blatcher, Maria
Paulsen, Janet E.
Pausch, Mark H.
机构
[1] Wyeth Res, Biol Technol, Cambridge, MA 02140 USA
[2] Wyeth Res, Neurosci, Princeton, NJ 08543 USA
关键词
orphan GPCR; in situ hybridization; yeast; chimeric G protein; reporter gene assay;
D O I
10.1016/j.brainres.2006.02.123
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
This report describes the identification and characterization of the murine orphan GPCR, Gpr101. Both human and murine genes were localized to chromosome X. Similar to its human ortholog, murine Gpr101 mRNA was detected predominantly in the brain within discrete nuclei. A knowledge-restricted hidden Markov model-based algorithm, capable of accurately predicting G-protein coupling selectivity, indicated that both human and murine GPR101 were likely coupled to Gs. This prediction was supported by the elevation of cyclic AMP levels and the activation of a cyclic AMP response element-luciferase reporter gene in HEK293 cells over-expressing human GPR101. Consistent with this, over-expression of human GPR101 in a yeast-based system yielded an elevated, agonist-independent reporter gene response in the presence of a yeast chimeric Gas protein. These results indicate that GPR101 participates in a potentially wide range of activities in the CNS via modulation of cAMP levels. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 14
页数:14
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