Department of Molecular Biology and Genetics, Koc University, Istanbul, Turkey.
PLoS Biol. 2020 Jun 18;18(6):e3000679. doi: 10.1371/journal.pbio.3000679. eCollection 2020 Jun.
Centriolar satellites are dynamic, membraneless granules composed of over 200 proteins. They store, modify, and traffic centrosome and primary cilium proteins, and help to regulate both the biogenesis and some functions of centrosomes and cilium. In most cell types, satellites cluster around the perinuclear centrosome, but their integrity and cellular distribution are dynamically remodeled in response to different stimuli, such as cell cycle cues. Dissecting the specific and temporal functions and mechanisms of satellites and how these are influenced by their cellular positioning and dynamics has been challenging using genetic approaches, particularly in ciliated and proliferating cells. To address this, we developed a chemical-based trafficking assay to rapidly and efficiently redistribute satellites to either the cell periphery or center, and fuse them into stable clusters in a temporally controlled way. Induced satellite clustering at either the periphery or center resulted in antagonistic changes in the pericentrosomal levels of a subset of proteins, revealing a direct and selective role for their positioning in protein targeting and sequestration. Systematic analysis of the interactome of peripheral satellite clusters revealed enrichment of proteins implicated in cilium biogenesis and mitosis. Importantly, induction of peripheral satellite targeting in ciliated cells revealed a function for satellites not just for efficient cilium assembly but also in the maintenance of steady-state cilia and in cilia disassembly by regulating the structural integrity of the ciliary axoneme. Finally, perturbing satellite distribution and dynamics inhibited their mitotic dissolution, and mitotic progression was perturbed only in cells with centrosomal satellite clustering. Collectively, our results for the first time showed a direct link between satellite functions and their pericentrosomal clustering, suggested new mechanisms underlying satellite functions during cilium assembly, and provided a new tool for probing temporal satellite functions in different contexts.
中心体卫星是由超过 200 种蛋白质组成的动态、无膜颗粒。它们储存、修饰和运输中心体和初级纤毛蛋白,并有助于调节中心体和纤毛的生物发生和某些功能。在大多数细胞类型中,卫星围绕核周中心体聚集,但它们的完整性和细胞分布会根据不同的刺激(如细胞周期信号)进行动态重塑。使用遗传方法解析卫星的特定和时间功能和机制,以及它们如何受到细胞定位和动力学的影响,一直具有挑战性,特别是在纤毛和增殖细胞中。为了解决这个问题,我们开发了一种基于化学的运输测定法,以快速有效地将卫星重新分配到细胞边缘或中心,并以时间控制的方式将它们融合到稳定的簇中。在外周或中心诱导卫星聚集会导致中心体周围一组蛋白质的水平发生拮抗变化,这揭示了它们在蛋白质靶向和隔离中的定位直接且具有选择性作用。对周边卫星簇相互作用组的系统分析显示,富含与纤毛发生和有丝分裂相关的蛋白质。重要的是,在纤毛细胞中诱导外周卫星靶向,揭示了卫星的功能不仅在于有效组装纤毛,还在于通过调节纤毛轴突的结构完整性来维持稳态纤毛和在纤毛解聚中发挥作用。最后,扰乱卫星的分布和动力学会抑制它们的有丝分裂溶解,只有当中心体卫星聚集时,有丝分裂才会受到干扰。总的来说,我们的研究结果首次表明卫星功能与其中心体周围聚集之间存在直接联系,提出了卫星在纤毛组装过程中功能的新机制,并提供了一种新工具,可用于在不同背景下探测卫星的时间功能。