Sergin Ismail, Jong Yuh-Jiin I, Harmon Steven K, Kumar Vikas, O'Malley Karen L
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
J Biol Chem. 2017 Mar 3;292(9):3637-3655. doi: 10.1074/jbc.M116.757724. Epub 2017 Jan 17.
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.
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。