Suppr超能文献

人类C类G蛋白偶联受体第6组成员A(GPRC6A)中的基因变异控制细胞表面表达和功能。

Genetic Variations in the Human G Protein-coupled Receptor Class C, Group 6, Member A (GPRC6A) Control Cell Surface Expression and Function.

作者信息

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

机构信息

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.

出版信息

J Biol Chem. 2017 Jan 27;292(4):1524-1534. doi: 10.1074/jbc.M116.756577. Epub 2016 Dec 16.

Abstract

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.

摘要

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。

相似文献

2
Cloning and characterization of a family C orphan G-protein coupled receptor.
J Neurochem. 2005 Apr;93(2):383-91. doi: 10.1111/j.1471-4159.2005.03025.x.
4
Pharmacology and physiological function of the orphan GPRC6A receptor.
Basic Clin Pharmacol Toxicol. 2020 Jun;126 Suppl 6:77-87. doi: 10.1111/bcpt.13397. Epub 2020 Mar 3.
5
Human GPRC6A Mediates Testosterone-Induced Mitogen-Activated Protein Kinases and mTORC1 Signaling in Prostate Cancer Cells.
Mol Pharmacol. 2019 May;95(5):563-572. doi: 10.1124/mol.118.115014. Epub 2019 Mar 20.
6
The GPCR, class C, group 6, subtype A (GPRC6A) receptor: from cloning to physiological function.
Br J Pharmacol. 2014 Mar;171(5):1129-41. doi: 10.1111/bph.12365.
7
Pharmacological characterization of mouse GPRC6A, an L-alpha-amino-acid receptor modulated by divalent cations.
Br J Pharmacol. 2007 Mar;150(6):798-807. doi: 10.1038/sj.bjp.0707121. Epub 2007 Jan 22.
8
Deorphanization of GPRC6A: a promiscuous L-alpha-amino acid receptor with preference for basic amino acids.
Mol Pharmacol. 2005 Mar;67(3):589-97. doi: 10.1124/mol.104.007559. Epub 2004 Dec 2.
9
GPRC6A: Jack of all metabolism (or master of none).
Mol Metab. 2016 Dec 21;6(2):185-193. doi: 10.1016/j.molmet.2016.12.006. eCollection 2017 Feb.
10
Analysis of GPRC6A variants in different pancreatitis etiologies.
Pancreatology. 2020 Oct;20(7):1262-1267. doi: 10.1016/j.pan.2020.08.001. Epub 2020 Aug 8.

引用本文的文献

1
GPRC6A is a Potential Therapeutic Target for Metformin Regulation of Glucose Homeostasis in Mice.
bioRxiv. 2024 Aug 19:2024.08.19.608635. doi: 10.1101/2024.08.19.608635.
2
Identification of actionable targets for breast cancer intervention using a diversity outbred mouse model.
iScience. 2023 Mar 2;26(4):106320. doi: 10.1016/j.isci.2023.106320. eCollection 2023 Apr 21.
3
Advanced Therapeutic Options for Treatment of Metastatic Castration Resistant Prostatic Adenocarcinoma.
Front Pharmacol. 2021 Nov 10;12:728054. doi: 10.3389/fphar.2021.728054. eCollection 2021.
4
Skeletal endocrinology: where evolutionary advantage meets disease.
Bone Res. 2021 May 28;9(1):28. doi: 10.1038/s41413-021-00149-x.
5
Explaining Divergent Observations Regarding Osteocalcin/GPRC6A Endocrine Signaling.
Endocrinology. 2021 Apr 1;162(4). doi: 10.1210/endocr/bqab011.
6
Humanized GPRC6A is a gain-of-function polymorphism in mice.
Sci Rep. 2020 Jul 7;10(1):11143. doi: 10.1038/s41598-020-68113-z.
7
Role of GPRC6A in Regulating Hepatic Energy Metabolism in Mice.
Sci Rep. 2020 Apr 29;10(1):7216. doi: 10.1038/s41598-020-64384-8.
8
Metabolic and skeletal homeostasis are maintained in full locus GPRC6A knockout mice.
Sci Rep. 2019 Apr 12;9(1):5995. doi: 10.1038/s41598-019-41921-8.
9
Human GPRC6A Mediates Testosterone-Induced Mitogen-Activated Protein Kinases and mTORC1 Signaling in Prostate Cancer Cells.
Mol Pharmacol. 2019 May;95(5):563-572. doi: 10.1124/mol.118.115014. Epub 2019 Mar 20.
10
Osteocalcin‑GPRC6A: An update of its clinical and biological multi‑organic interactions (Review).
Mol Med Rep. 2019 Jan;19(1):15-22. doi: 10.3892/mmr.2018.9627. Epub 2018 Nov 5.

本文引用的文献

1
Robust GLP-1 secretion by basic L-amino acids does not require the GPRC6A receptor.
Diabetes Obes Metab. 2017 Apr;19(4):599-603. doi: 10.1111/dom.12845. Epub 2017 Jan 19.
2
L-arginine promotes gut hormone release and reduces food intake in rodents.
Diabetes Obes Metab. 2016 May;18(5):508-18. doi: 10.1111/dom.12644. Epub 2016 Apr 1.
3
Murine GPRC6A Mediates Cellular Responses to L-Amino Acids, but Not Osteocalcin Variants.
PLoS One. 2016 Jan 19;11(1):e0146846. doi: 10.1371/journal.pone.0146846. eCollection 2016.
4
The experimental power of FR900359 to study Gq-regulated biological processes.
Nat Commun. 2015 Dec 14;6:10156. doi: 10.1038/ncomms10156.
5
GPRC6a is not required for the effects of a high-protein diet on body weight in mice.
Obesity (Silver Spring). 2015 Jun;23(6):1194-200. doi: 10.1002/oby.21083. Epub 2015 May 9.
6
N-glycosylation and disulfide bonding affects GPRC6A receptor expression, function, and dimerization.
FEBS Lett. 2015 Feb 27;589(5):588-97. doi: 10.1016/j.febslet.2015.01.019. Epub 2015 Jan 21.
7
Generic GPCR residue numbers - aligning topology maps while minding the gaps.
Trends Pharmacol Sci. 2015 Jan;36(1):22-31. doi: 10.1016/j.tips.2014.11.001. Epub 2014 Dec 22.
8
Location-dependent signaling of the group 1 metabotropic glutamate receptor mGlu5.
Mol Pharmacol. 2014 Dec;86(6):774-85. doi: 10.1124/mol.114.094763. Epub 2014 Oct 17.
10
The GPCR, class C, group 6, subtype A (GPRC6A) receptor: from cloning to physiological function.
Br J Pharmacol. 2014 Mar;171(5):1129-41. doi: 10.1111/bph.12365.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验