Department of Cell Biology, University of Potsdam, Karl-Liebknecht-Str. 24-25, 14476 Potsdam-Golm, Germany.
Cells. 2024 Sep 10;13(18):1513. doi: 10.3390/cells13181513.
The centrosome of the amoebozoan model provides the best-established model for an acentriolar centrosome outside the . exhibits an unusual centrosome cycle, in which duplication is initiated only at the G2/M transition and occurs entirely during the M phase. Little is known about the role of conserved centrosomal kinases in this process. Therefore, we have generated knock-in strains for Aurora (AurK), CDK1, cyclin B, Nek2, and Plk, replacing the endogenous genes with constructs expressing the respective green fluorescent Neon fusion proteins, driven by the endogenous promoters, and studied their behavior in living cells. Our results show that CDK1 and cyclin B arrive at the centrosome first, already during G2, followed by Plk, Nek2, and AurK. Furthermore, CDK1/cyclin B and AurK were dynamically localized at kinetochores, and AurK in addition at nucleoli. The putative roles of all four kinases in centrosome duplication, mitosis, cytokinesis, and nucleolar dynamics are discussed.
肉足动物模型的中心体提供了最成熟的非中心粒中心体模型。 表现出异常的中心体周期,其中只有在 G2/M 转变时才开始复制,并且完全发生在 M 期。关于保守的中心体激酶在这个过程中的作用知之甚少。因此,我们已经为 Aurora(AurK)、CDK1、cyclin B、Nek2 和 Plk 生成了基因敲入株系,用表达各自的绿色荧光 Neon 融合蛋白的构建体替换内源性基因,由内源性启动子驱动,并在活细胞中研究它们的行为。我们的结果表明,CDK1 和 cyclin B 首先到达中心体,已经在 G2 期间,随后是 Plk、Nek2 和 AurK。此外,CDK1/cyclin B 和 AurK 被动态定位于动粒上,此外 AurK 还定位于核仁上。讨论了这四种激酶在中心体复制、有丝分裂、胞质分裂和核仁动力学中的潜在作用。