Max Perutz Labs, University of Vienna, Vienna Biocenter (VBC), Dr. Bohr-Gasse 9, A-1030 Vienna, Austria.
Institut Jacques Monod, CNRS, UMR 7592, University Paris Diderot, Sorbonne Paris Cité, 75205 Paris, France.
Dev Cell. 2019 Aug 5;50(3):355-366.e6. doi: 10.1016/j.devcel.2019.06.004. Epub 2019 Jul 11.
Centrosomes, the predominant sites of microtubule nucleation and anchorage, coordinate spindle assembly and cell division in animal cells. At the onset of mitosis, centrioles accumulate microtubule-organizing pericentriolar material (PCM) in a process termed centrosome maturation. To what extent centrosome maturation depends on the continued activity of mitotic regulators or the presence of centrioles has hitherto been unclear. Using the C. elegans early embryo, we show that PCM expansion requires the Polo-like kinase PLK-1 and CEP192 (SPD-2 in C. elegans), but not its upstream regulator Aurora A (AIR-1), while maintenance of the PCM polymer depends exclusively on PLK-1. SPD-2 and PLK-1 are highly concentrated at centrioles. Unexpectedly, laser microsurgery reveals that while centrioles are required for PCM recruitment and centrosome structural integrity they are dispensable for PCM maintenance. We propose a model whereby centrioles promote centrosome maturation by recruiting PLK-1, but subsequent maintenance occurs via PLK-1 acting directly within the PCM.
中心体是微管起始和锚定的主要场所,在动物细胞中协调纺锤体组装和细胞分裂。在有丝分裂开始时,中心体在一个称为中心体成熟的过程中积累微管组织中心周围物质(PCM)。到目前为止,中心体成熟在多大程度上依赖于有丝分裂调节剂的持续活性或中心体的存在还不清楚。使用秀丽隐杆线虫早期胚胎,我们表明 PCM 扩展需要 Polo 样激酶 PLK-1 和 CEP192(秀丽隐杆线虫中的 SPD-2),但不需要其上游调节剂 Aurora A(AIR-1),而 PCM 聚合物的维持则完全依赖于 PLK-1。SPD-2 和 PLK-1 高度集中在中心体上。出乎意料的是,激光微手术显示,尽管中心体对于 PCM 的募集和中心体结构完整性是必需的,但对于 PCM 的维持却是可有可无的。我们提出了一个模型,其中中心体通过招募 PLK-1 来促进中心体成熟,但随后的维持是通过 PLK-1 在 PCM 内直接作用来实现的。