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人细胞中Plk4诱导的中心粒生物发生。

Plk4-induced centriole biogenesis in human cells.

作者信息

Kleylein-Sohn Julia, Westendorf Jens, Le Clech Mikael, Habedanck Robert, Stierhof York-Dieter, Nigg Erich A

机构信息

Department of Cell Biology, Max-Planck Institute of Biochemistry, Am Klopferspitz 18, D-82152 Martinsried, Germany.

出版信息

Dev Cell. 2007 Aug;13(2):190-202. doi: 10.1016/j.devcel.2007.07.002.

Abstract

We show that overexpression of Polo-like kinase 4 (Plk4) in human cells induces centrosome amplification through the simultaneous generation of multiple procentrioles adjoining each parental centriole. This provided an opportunity for dissecting centriole assembly and characterizing assembly intermediates. Critical components were identified and ordered into an assembly pathway through siRNA and localized through immunoelectron microscopy. Plk4, hSas-6, CPAP, Cep135, gamma-tubulin, and CP110 were required at different stages of procentriole formation and in association with different centriolar structures. Remarkably, hSas-6 associated only transiently with nascent procentrioles, whereas Cep135 and CPAP formed a core structure within the proximal lumen of both parental and nascent centrioles. Finally, CP110 was recruited early and then associated with the growing distal tips, indicating that centrioles elongate through insertion of alpha-/beta-tubulin underneath a CP110 cap. Collectively, these data afford a comprehensive view of the assembly pathway underlying centriole biogenesis in human cells.

摘要

我们发现,在人类细胞中过表达Polo样激酶4(Plk4)会通过在每个亲代中心粒旁同时生成多个原中心粒来诱导中心体扩增。这为剖析中心粒组装过程并鉴定组装中间体提供了契机。通过小干扰RNA(siRNA)鉴定出关键组分并将其排列成组装途径,通过免疫电子显微镜对其进行定位。在原中心粒形成的不同阶段以及与不同中心粒结构相关联时,需要Plk4、hSas-6、中心体相关蛋白(CPAP)、Cep135、γ-微管蛋白和CP110。值得注意的是,hSas-6仅与新生原中心粒短暂结合,而Cep135和CPAP在亲代和新生中心粒的近端管腔内形成核心结构。最后,CP110被早期招募,然后与不断生长的远端末端相关联,这表明中心粒通过在CP110帽下方插入α/β-微管蛋白而延长。总体而言,这些数据提供了人类细胞中中心粒生物发生基础组装途径的全面视图。

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