Characterization of an orphan G protein-coupled receptor localized in the dorsal root ganglia reveals adenine as a signaling molecule

被引:109
作者
Bender, E
Buist, A
Jurzak, M
Langlois, X
Baggerman, G
Verhasselt, P
Ercken, M
Guo, HQ
Wintmolders, C
Van den Wyngaert, I
Van Oers, I
Schoofs, L
Luyten, W
机构
[1] Janssen Pharmaceut, Dept Cent Nervous Syst Discovery Res, Johnson & Johnson Pharmaceut Res & Dev, B-2340 Beerse, Belgium
[2] Janssen Pharmaceut, Dept Adv Biotechnol, Johnson & Johnson Pharmaceut Res & Dev, B-2340 Beerse, Belgium
[3] Janssen Pharmaceut, Dept Assay Dev & High Throughput Screening, Johnson & Johnson Pharmaceut Res & Dev, B-2340 Beerse, Belgium
[4] Janssen Pharmaceut, Dept Appl Biotechnol, Johnson & Johnson Pharmaceut Res & Dev, B-2340 Beerse, Belgium
[5] Katholieke Univ Leuven, Lab Dev Physiol & Mol Biol, B-3000 Leuven, Belgium
[6] Johnson & Johnson Pharmaceut Res & Dev, Dept Neurosci, San Diego, CA 92121 USA
关键词
D O I
10.1073/pnas.122016499
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The cloning of novel G protein-coupled receptors and the search for their natural ligands, a process called reverse pharmacology, is an excellent opportunity to discover novel hormones and neurotransmitters. Based on a degenerate primer approach we have cloned a G protein-coupled receptor whose mRNA expression profile indicates highest expression in the dorsal root ganglia, specifically in the subset of small neurons, suggesting a role in nociception. In addition, moderate expression was found in lung, hypothalamus, peripheral blood leukocytes, and ovaries. Guided by a receptor-activation bioassay, we identified adenine as the endogenous ligand, which activated the receptor potently and with high structural stringency. Therefore, we propose to name this receptor as the adenine receptor. Hormonal functions have already been demonstrated for adenine derivatives like 6-benzylaminopurine in plants and 1-methyladenine in lower animals. Here, we demonstrate that adenine functions as a signaling molecule in mammals. This finding adds a third family besides P1 and P2 receptors to the class of purinergic receptors.
引用
收藏
页码:8573 / 8578
页数:6
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