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Nat Commun. 2016 Feb 3;7:10604. doi: 10.1038/ncomms10604.
2
Access of torsinA to the inner nuclear membrane is activity dependent and regulated in the endoplasmic reticulum.扭转蛋白A进入内核膜是依赖活性的,并在内质网中受到调控。
J Cell Sci. 2015 Aug 1;128(15):2854-65. doi: 10.1242/jcs.167452. Epub 2015 Jun 19.
3
PDZ Protein Regulation of G Protein-Coupled Receptor Trafficking and Signaling Pathways.PDZ蛋白对G蛋白偶联受体转运及信号通路的调控
Mol Pharmacol. 2015 Oct;88(4):624-39. doi: 10.1124/mol.115.098509. Epub 2015 Mar 25.
4
G protein-coupled receptor signaling in cardiac nuclear membranes.心脏核膜中的G蛋白偶联受体信号传导
J Cardiovasc Pharmacol. 2015 Feb;65(2):101-9. doi: 10.1097/FJC.0000000000000196.
5
Nuclear G protein signaling: new tricks for old dogs.细胞核G蛋白信号传导:老方法新应用
J Cardiovasc Pharmacol. 2015 Feb;65(2):110-22. doi: 10.1097/FJC.0000000000000198.
6
Glycan regulation of ER-associated degradation through compartmentalization.糖基化通过区室化调节内质网相关降解。
Semin Cell Dev Biol. 2015 May;41:99-109. doi: 10.1016/j.semcdb.2014.11.006. Epub 2014 Nov 24.
7
Location-dependent signaling of the group 1 metabotropic glutamate receptor mGlu5.1型代谢型谷氨酸受体mGlu5的位置依赖性信号传导
Mol Pharmacol. 2014 Dec;86(6):774-85. doi: 10.1124/mol.114.094763. Epub 2014 Oct 17.
8
Trafficking and function of GPCRs in the endosomal compartment.G蛋白偶联受体(GPCRs)在内体区室中的运输与功能
Methods Mol Biol. 2015;1234:197-211. doi: 10.1007/978-1-4939-1755-6_16.
9
Subcellular localization of coagulation factor II receptor-like 1 in neurons governs angiogenesis.神经元中凝血因子 II 受体样 1 的亚细胞定位控制血管生成。
Nat Med. 2014 Oct;20(10):1165-73. doi: 10.1038/nm.3669. Epub 2014 Sep 14.
10
GPCR signaling along the endocytic pathway.G 蛋白偶联受体沿着内吞途径的信号转导。
Curr Opin Cell Biol. 2014 Apr;27:109-16. doi: 10.1016/j.ceb.2013.10.003. Epub 2013 Dec 28.

代谢型谷氨酸受体5(mGluR5)C末端的序列负责其在内核膜的定位。

Sequences within the C Terminus of the Metabotropic Glutamate Receptor 5 (mGluR5) Are Responsible for Inner Nuclear Membrane Localization.

作者信息

Sergin Ismail, Jong Yuh-Jiin I, Harmon Steven K, Kumar Vikas, O'Malley Karen L

机构信息

From the Department of Neuroscience, Washington University School of Medicine, St. Louis, Missouri 63110.

From the Department of Neuroscience, Washington University School of Medicine, St. Louis, Missouri 63110

出版信息

J Biol Chem. 2017 Mar 3;292(9):3637-3655. doi: 10.1074/jbc.M116.757724. Epub 2017 Jan 17.

DOI:10.1074/jbc.M116.757724
PMID:28096465
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5339749/
Abstract

Traditionally, G-protein-coupled receptors (GPCR) are thought to be located on the cell surface where they transmit extracellular signals to the cytoplasm. However, recent studies indicate that some GPCRs are also localized to various subcellular compartments such as the nucleus where they appear required for various biological functions. For example, the metabotropic glutamate receptor 5 (mGluR5) is concentrated at the inner nuclear membrane (INM) where it mediates Ca changes in the nucleoplasm by coupling with G Here, we identified a region within the C-terminal domain (amino acids 852-876) that is necessary and sufficient for INM localization of the receptor. Because these sequences do not correspond to known nuclear localization signal motifs, they represent a new motif for INM trafficking. mGluR5 is also trafficked to the plasma membrane where it undergoes re-cycling/degradation in a separate receptor pool, one that does not interact with the nuclear mGluR5 pool. Finally, our data suggest that once at the INM, mGluR5 is stably retained via interactions with chromatin. Thus, mGluR5 is perfectly positioned to regulate nucleoplasmic Ca.

摘要

传统上,人们认为G蛋白偶联受体(GPCR)位于细胞表面,在那里它们将细胞外信号传递到细胞质。然而,最近的研究表明,一些GPCR也定位于各种亚细胞区室,如细胞核,在那里它们似乎是各种生物学功能所必需的。例如,代谢型谷氨酸受体5(mGluR5)集中在内核膜(INM)上,在那里它通过与G偶联介导核质中的Ca变化。在这里,我们在C末端结构域(氨基酸852 - 876)内鉴定出一个区域,该区域对于受体的INM定位是必要且充分的。由于这些序列与已知的核定位信号基序不对应,它们代表了一种新的INM运输基序。mGluR5也被运输到质膜,在那里它在一个独立的受体池中进行再循环/降解,这个受体池不与核mGluR5池相互作用。最后,我们的数据表明,一旦到达INM,mGluR5通过与染色质的相互作用而稳定保留。因此,mGluR5处于完美的位置来调节核质Ca。