Smith K E, Walker M W, Artymyshyn R, Bard J, Borowsky B, Tamm J A, Yao W J, Vaysse P J, Branchek T A, Gerald C, Jones K A
Departments of Molecular Biology and Pharmacology, Synaptic Pharmaceutical Corporation, Paramus, New Jersey 07652, USA.
J Biol Chem. 1998 Sep 4;273(36):23321-6. doi: 10.1074/jbc.273.36.23321.
The neuropeptide galanin has been implicated in the regulation of processes such as nociception, cognition, feeding behavior, and hormone secretion. Multiple galanin receptors are predicted to mediate its effects, but only two functionally coupled receptors have been reported. We now report the cloning of a third galanin receptor distinct from GALR1 and GALR2. The receptor, termed GALR3, was isolated from a rat hypothalamus cDNA library by both expression and homology cloning approaches. The rat GALR3 receptor cDNA can encode a protein of 370 amino acids with 35% and 52% identity to GALR1 and GALR2, respectively. Localization of mRNA by solution hybridization/RNase protection demonstrates that the GALR3 transcript is widely distributed, but expressed at low abundance, with the highest levels in the hypothalamus and pituitary. We also isolated the gene encoding the human homologue of GALR3. The human GALR3 receptor is 90% identical to rat GALR3 and contains 368 amino acids. Binding of porcine 125I-galanin to stably expressed rat and human GALR3 receptors is saturable (rat KD = 0.98 nM and human KD = 2.23 nM) and displaceable by galanin peptides and analogues in the following rank order: rat galanin, porcine galanin approximately M32, M35 approximately porcine galanin-(-7 to +29), galantide, human galanin > M40, galanin-(1-16) > [D-Trp2]galanin-(1-29), galanin-(3-29). This profile resembles that of the rat GALR1 and GALR2 receptors with the notable exception that human galanin, galanin-(1-16), and M40 show lower affinity at GALR3. In Xenopus oocytes, activation of rat and human GALR3 receptors co-expressed with potassium channel subunits GIRK1 and GIRK4 resulted in inward K+ currents characteristic of Gi/Go-coupled receptors. These data confirm the functional efficacy of GALR3 receptors and further suggest that GALR3 signaling pathways resemble those of GALR1 in that both can activate potassium channels linked to the regulation of neurotransmitter release.
神经肽甘丙肽与伤害感受、认知、摄食行为和激素分泌等过程的调节有关。预计多种甘丙肽受体介导其作用,但仅报道了两种功能偶联受体。我们现在报告克隆了一种不同于GALR1和GALR2的第三种甘丙肽受体。该受体称为GALR3,通过表达克隆和同源克隆方法从大鼠下丘脑cDNA文库中分离得到。大鼠GALR3受体cDNA可编码一种370个氨基酸的蛋白质,与GALR1和GALR2的同源性分别为35%和52%。通过溶液杂交/核糖核酸酶保护法对mRNA进行定位显示,GALR3转录本广泛分布,但表达丰度较低,在下丘脑和垂体中水平最高。我们还分离了编码人类GALR3同源物的基因。人类GALR3受体与大鼠GALR3的同源性为90%,含有368个氨基酸。猪125I-甘丙肽与稳定表达的大鼠和人类GALR3受体的结合是可饱和的(大鼠KD = 0.98 nM,人类KD = 2.23 nM),并且可被甘丙肽肽和类似物以以下顺序取代:大鼠甘丙肽、猪甘丙肽≈M32、M35≈猪甘丙肽-(-7至+29)、甘丙肽拮抗剂、人类甘丙肽>M40、甘丙肽-(1-16)>[D-色氨酸2]甘丙肽-(1-29)、甘丙肽-(3-29)。该谱与大鼠GALR1和GALR2受体的谱相似,但显著的例外是人类甘丙肽、甘丙肽-(1-16)和M40在GALR3上显示出较低的亲和力。在非洲爪蟾卵母细胞中,与钾通道亚基GIRK1和GIRK4共表达的大鼠和人类GALR3受体的激活导致了Gi/Go偶联受体特有的内向K+电流。这些数据证实了GALR3受体的功能有效性,并进一步表明GALR3信号通路与GALR1的信号通路相似,因为两者都可以激活与神经递质释放调节相关的钾通道。