Department of Cell Biology, University of Potsdam, Karl-Liebknecht-Str. 24-25, 14476 Potsdam-Golm, Germany.
Department of Animal Physiology, University of Potsdam, Karl-Liebknecht-Str. 24-25, 14476 Potsdam-Golm, Germany.
Cells. 2021 Sep 10;10(9):2384. doi: 10.3390/cells10092384.
The centrosome is a nucleus-associated body with a diameter of approx. 500 nm. It contains no centrioles but consists of a cylindrical layered core structure surrounded by a microtubule-nucleating corona. At the onset of mitosis, the corona disassembles and the core structure duplicates through growth, splitting, and reorganization of the outer core layers. During the last decades our research group has characterized the majority of the 42 known centrosomal proteins. In this work we focus on the conserved, previously uncharacterized Cep192 protein. We use superresolution expansion microscopy (ExM) to show that Cep192 is a component of the outer core layers. Furthermore, ExM with centrosomal marker proteins nicely mirrored all ultrastructurally known centrosomal substructures. Furthermore, we improved the proximity-dependent biotin identification assay (BioID) by adapting the biotinylase BioID2 for expression in and applying a knock-in strategy for the expression of BioID2-tagged centrosomal fusion proteins. Thus, we were able to identify various centrosomal Cep192 interaction partners, including CDK5RAP2, which was previously allocated to the inner corona structure, and several core components. Studies employing overexpression of GFP-Cep192 as well as depletion of endogenous Cep192 revealed that Cep192 is a key protein for the recruitment of corona components during centrosome biogenesis and is required to maintain a stable corona structure.
中心体是一种直径约为 500nm 的核相关体。它不含中心粒,而是由一个圆柱形分层核心结构组成,周围环绕着一个微管起始冠。在有丝分裂开始时,冠解聚,核心结构通过外层核心层的生长、分裂和重组进行复制。在过去的几十年里,我们的研究小组已经对大多数 42 种已知的中心体蛋白进行了特征描述。在这项工作中,我们专注于保守的、以前未被描述的 Cep192 蛋白。我们使用超分辨率扩展显微镜(ExM)来显示 Cep192 是外层核心层的一个组成部分。此外,用中心体标记蛋白的 ExM 很好地反映了所有超微结构上已知的中心体亚结构。此外,我们通过将生物素酶 BioID2 适应于在 中表达,并应用 BioID2 标记的中心体融合蛋白的敲入策略,改进了依赖邻近性的生物素鉴定测定法(BioID)。因此,我们能够鉴定出各种中心体 Cep192 相互作用伙伴,包括以前被分配到内冠结构的 CDK5RAP2 和几个核心成分。研究表明,GFP-Cep192 的过表达以及内源性 Cep192 的耗竭表明,Cep192 是在中心体发生过程中招募冠组件的关键蛋白,并且对于维持稳定的冠结构是必需的。