Department of Biochemistry, School of Medicine, Autonomous University of Madrid (UAM), Madrid, Spain.
Instituto de Investigaciones Biomédicas Alberto Sols, CSIC-UAM, Madrid, Spain.
Biochem Soc Trans. 2021 Feb 26;49(1):79-91. doi: 10.1042/BST20191005.
Primary cilia are hair-like projections of the cell membrane supported by an inner microtubule scaffold, the axoneme, which polymerizes out of a membrane-docked centriole at the ciliary base. By working as specialized signaling compartments, primary cilia provide an optimal environment for many G protein-coupled receptors (GPCRs) and their effectors to efficiently transmit their signals to the rest of the cell. For this to occur, however, all necessary receptors and signal transducers must first accumulate at the ciliary membrane. Serotonin receptor 6 (HTR6) and Somatostatin receptor 3 (SSTR3) are two GPCRs whose signaling in brain neuronal cilia affects cognition and is implicated in psychiatric, neurodegenerative, and oncologic diseases. Over a decade ago, the third intracellular loops (IC3s) of HTR6 and SSTR3 were shown to contain ciliary localization sequences (CLSs) that, when grafted onto non-ciliary GPCRs, could drive their ciliary accumulation. Nevertheless, these CLSs were dispensable for ciliary targeting of HTR6 and SSTR3, suggesting the presence of additional CLSs, which we have recently identified in their C-terminal tails. Herein, we review the discovery and mapping of these CLSs, as well as the state of the art regarding how these CLSs may orchestrate ciliary accumulation of these GPCRs by controlling when and where they interact with the ciliary entry and exit machinery via adaptors such as TULP3, RABL2 and the BBSome.
原发性纤毛是细胞膜向外突出的毛发状结构,由内微管支架轴丝支撑,轴丝从位于纤毛基部的膜结合中心粒上聚合而成。作为专门的信号转导隔室,原发性纤毛为许多 G 蛋白偶联受体(GPCR)及其效应器提供了最佳环境,使其能够有效地将信号传递到细胞的其余部分。然而,要做到这一点,所有必需的受体和信号转导器必须首先积累在纤毛膜上。5-羟色胺受体 6(HTR6)和生长抑素受体 3(SSTR3)是两种 GPCR,它们在脑神经元纤毛中的信号转导会影响认知,并与精神疾病、神经退行性疾病和肿瘤疾病有关。十多年前,HTR6 和 SSTR3 的第三细胞内环(IC3)被证明含有纤毛定位序列(CLS),当将其嫁接在非纤毛 GPCR 上时,可以驱动其纤毛积累。然而,这些 CLS 对于 HTR6 和 SSTR3 的纤毛靶向是可有可无的,这表明存在其他 CLS,我们最近在它们的 C 末端尾巴中发现了这些 CLS。在此,我们回顾了这些 CLS 的发现和映射,以及关于这些 CLS 如何通过控制它们与纤毛进入和退出机械的相互作用的时间和地点来协调这些 GPCR 的纤毛积累的最新进展,这种相互作用是通过衔接蛋白如 TULP3、RABL2 和 BBSome 来实现的。