Graser Susanne, Stierhof York-Dieter, Nigg Erich A
Max-Planck-Institute for Biochemistry, Department of Cell Biology, Am Klopferspitz 18, D-82152 Martinsried, Germany.
J Cell Sci. 2007 Dec 15;120(Pt 24):4321-31. doi: 10.1242/jcs.020248. Epub 2007 Nov 27.
The centrosome duplicates during the cell cycle but functions as a single microtubule-organising centre until shortly before mitosis. This raises the question of how centrosome cohesion is maintained throughout interphase. One dynamic model proposes that parental centrioles are held together through centriole-associated, entangling filaments. Central to this model are C-Nap1, a putative centriolar docking protein and rootletin, a fibrous component. Here we identify two novel proteins, Cep68 and Cep215, as required for centrosome cohesion. Similar to rootletin, Cep68 decorates fibres emanating from the proximal ends of centrioles and dissociates from centrosomes during mitosis. Furthermore, Cep68 and rootletin depend both on each other and on C-Nap1 for centriole association. Unlike rootletin, overexpression of Cep68 does not induce extensive fibre formation, but Cep68 is readily recruited to ectopic rootletin fibres. These data suggest that Cep68 cooperates with rootletin and C-Nap1 in centrosome cohesion. By contrast, Cep215 associates with centrosomes throughout the cell cycle and does not appear to interact with Cep68, rootletin or C-Nap1. Instead, our data suggest that Cep215 functionally interacts with pericentrin, suggesting that both proteins influence centrosome cohesion through an indirect mechanism related to cytoskeletal dynamics.
中心体在细胞周期中进行复制,但在有丝分裂前不久之前一直作为单个微管组织中心发挥作用。这就提出了一个问题,即在整个间期中心体的凝聚力是如何维持的。一种动态模型提出,亲代中心粒通过与中心粒相关的缠绕细丝结合在一起。该模型的核心是C-Nap1(一种假定的中心粒对接蛋白)和根蛋白(一种纤维成分)。在这里,我们鉴定出两种新的蛋白质Cep68和Cep215是中心体凝聚所必需的。与根蛋白类似,Cep68装饰从中心粒近端发出的纤维,并在有丝分裂期间从中心体解离。此外,Cep68和根蛋白在中心粒结合方面相互依赖且都依赖于C-Nap1。与根蛋白不同,Cep68的过表达不会诱导大量纤维形成,但Cep68很容易被招募到异位的根蛋白纤维上。这些数据表明,Cep68在中心体凝聚中与根蛋白和C-Nap1协同作用。相比之下,Cep215在整个细胞周期中都与中心体相关联,并且似乎不与Cep68、根蛋白或C-Nap1相互作用。相反,我们的数据表明,Cep215在功能上与中心体周围蛋白相互作用,这表明这两种蛋白质都通过与细胞骨架动力学相关的间接机制影响中心体的凝聚力。