Jørgensen Stine, Have Christian Theil, Underwood Christina Rye, Johansen Lars Dan, Wellendorph Petrine, Gjesing Anette Prior, Jørgensen Christinna V, Quan Shi, Rui Gao, Inoue Asuka, Linneberg Allan, Grarup Niels, Jun Wang, Pedersen Oluf, Hansen Torben, Bräuner-Osborne Hans
From the Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, DK-2100 Copenhagen, Denmark.
the Novo Nordisk Foundation Center for Basic Metabolic Research, Section of Metabolic Genetics, Faculty of Health and Medical Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark.
J Biol Chem. 2017 Jan 27;292(4):1524-1534. doi: 10.1074/jbc.M116.756577. Epub 2016 Dec 16.
GPRC6A is a G protein-coupled receptor activated by l-amino acids, which, based on analyses of knock-out mice, has been suggested to have physiological functions in metabolism and testicular function. The human ortholog is, however, mostly retained intracellularly in contrast to the cell surface-expressed murine and goldfish orthologs. The latter orthologs are G-coupled and lead to intracellular accumulation of inositol phosphates and calcium release. In the present study we cloned the bonobo chimpanzee GPRC6A receptor, which is 99% identical to the human receptor, and show that it is cell surface-expressed and functional. By analyses of chimeric human/mouse and human/bonobo receptors, bonobo receptor mutants, and the single nucleotide polymorphism database at NCBI, we identify an insertion/deletion variation in the third intracellular loop responsible for the intracellular retention and lack of function of the human ortholog. Genetic analyses of the 1000 genome database and the Inter99 cohort of 6,000 Danes establish the distribution of genotypes among ethnic groups, showing that the cell surface-expressed and functional variant is much more prevalent in the African population than in European and Asian populations and that this variant is partly linked with a stop codon early in the receptor sequence (rs6907580, amino acid position 57). In conclusion, our data solve a more than decade-old question of why the cloned human GPRC6A receptor is not cell surface-expressed and functional and provide a genetic framework to study human phenotypic traits in large genome sequencing projects linked with physiological measurement and biomarkers.
GPRC6A是一种由L-氨基酸激活的G蛋白偶联受体,基于对基因敲除小鼠的分析,提示其在代谢和睾丸功能中具有生理功能。然而,与细胞表面表达的小鼠和金鱼直系同源物相比,人类直系同源物大多保留在细胞内。后者的直系同源物是G偶联的,会导致肌醇磷酸在细胞内积累并释放钙。在本研究中,我们克隆了与人类受体有99%同一性的倭黑猩猩GPRC6A受体,并表明它在细胞表面表达且具有功能。通过对嵌合的人/小鼠和人/倭黑猩猩受体、倭黑猩猩受体突变体以及NCBI的单核苷酸多态性数据库进行分析,我们确定了第三个细胞内环中的一个插入/缺失变异,该变异导致了人类直系同源物的细胞内保留和功能缺失。对千人基因组数据库和6000名丹麦人的Inter99队列进行基因分析,确定了不同种族群体中的基因型分布,表明细胞表面表达且有功能的变异在非洲人群中比在欧洲和亚洲人群中更为普遍,并且该变异部分与受体序列早期的一个终止密码子(rs6907580,氨基酸位置57)相关。总之,我们的数据解决了一个十多年来的问题,即为什么克隆的人类GPRC6A受体不在细胞表面表达且无功能,并为在与生理测量和生物标志物相关的大型基因组测序项目中研究人类表型特征提供了一个遗传框架。