Department of Anatomy and Neurobiology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
J Neuroendocrinol. 2011 Sep;23(9):791-803. doi: 10.1111/j.1365-2826.2011.02179.x.
Several neuropeptides with the C-terminal Arg-Phe-NH(2) (RFa) sequence have been identified in the hypothalamus of a variety of vertebrates. The present study was conducted to isolate novel RFa peptides from the zebra finch brain. Peptides were isolated by immunoaffinity purification using an antibody that recognises avian RFa peptides. The isolated peptide consisted of 25 amino acids with RFa at its C-terminus. The sequence was SGTLGNLAEEINGYNRRKGGFTFRFa. Alignment of the peptide with vertebrate 26RFa has revealed that the identified peptide is the zebra finch 26RFa. We also cloned the precursor cDNA encoding this peptide. Synteny analysis of the gene showed a high conservation of this gene among vertebrates. In addition, we cloned the cDNA encoding a putative 26RFa receptor, G protein-coupled receptor 103 (GPR103) in the zebra finch brain. GPR103 cDNA encoded a 432 amino acid protein that has seven transmembrane domains. In situ hybridisation analysis in the brain showed that the expression of 26RFa mRNA is confined to the anterior-medial hypothalamic area, ventromedial nucleus of the hypothalamus and the lateral hypothalamic area, the brain regions that are involved in the regulation of feeding behaviour, whereas GPR103 mRNA is distributed throughout the brain in addition to the hypothalamic nuclei. When administered centrally in free-feeding male zebra finches, 26RFa increased food intake 24 h after injection without body mass change. Diencephalic GPR103 mRNA expression was up-regulated by fasting for 10 h. Our data suggest that the hypothalamic 26RFa-its receptor system plays an important role in the central control of food intake and energy homeostasis in the zebra finch.
几种带有 C 末端 Arg-Phe-NH2(RFa)序列的神经肽已在多种脊椎动物的下丘脑被鉴定出来。本研究旨在从斑马雀脑中分离出新的 RFa 肽。使用识别禽 RFa 肽的抗体通过免疫亲和纯化分离肽。分离出的肽由 25 个氨基酸组成,C 末端为 RFa。序列为 SGTLGNLAEEINGYNRRKGGFTFRFa。该肽与脊椎动物 26RFa 的序列比对表明,鉴定出的肽是斑马雀 26RFa。我们还克隆了编码这种肽的前体 cDNA。基因的基因分析表明,该基因在脊椎动物中高度保守。此外,我们克隆了编码斑马雀脑中假定 26RFa 受体 G 蛋白偶联受体 103(GPR103)的 cDNA。GPR103 cDNA 编码一个 432 个氨基酸的蛋白质,具有七个跨膜结构域。脑内原位杂交分析显示,26RFa mRNA 的表达局限于下丘脑前-中区域、下丘脑腹内侧核和外侧下丘脑区域,这些区域参与了摄食行为的调节,而 GPR103 mRNA 除了在下丘脑核外,还分布于整个脑内。在自由喂养的雄性斑马雀中中枢给药后,26RFa 在注射后 24 小时增加食物摄入量,而体重没有变化。禁食 10 小时可上调间脑 GPR103 mRNA 的表达。我们的数据表明,下丘脑 26RFa-其受体系统在斑马雀的中枢控制食物摄入和能量平衡中起着重要作用。