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Nek2-mediated GAS2L1 phosphorylation and centrosome-linker disassembly induce centrosome disjunction

机译:Nek2介导的Gas2L1磷酸化和中心组 - 连接器拆卸诱导中心组分离

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Centrosome disjunction occurs in late G2 to facilitate bipolar spindle formation and is mediated by the NIMA-related kinase Nek2. Here, we show that GAS2L1, a microtubule- and F-actin–binding protein required for centrosome disjunction, undergoes Nek2-mediated phosphorylation at Ser352 in G2/M. The phosphorylation is essential for centrosome disjunction in late G2 and for proper spindle assembly and faithful chromosome segregation in mitosis. GAS2L1 contains a calponin-homology (CH) domain and a GAS2-related (GAR) domain, which bind to F-actin and microtubules, respectively. Notably, the CH and GAR domains bind to each other to inhibit the functions of both domains, and Ser352 phosphorylation disrupts the interaction between the two domains and relieves the autoinhibition. We dissected the roles of the GAS2L1 phosphorylation and of centrosome-linker disassembly, which is another Nek2-mediated event, and found that these events together trigger centrosome disjunction. Therefore, our findings demonstrate the concerted Nek2 actions that split the centrosomes in late G2.
机译:在G2晚期的中心脱位发生,以促进双极主轴形成,并由Nima相关激酶Nek2介导。在这里,我们表明,气体2L1,微管和F-肌动蛋白结合蛋白所需的中心脱位所需,在G2 / m中的SER352处经历NEK2介导的磷酸化。磷酸化对于G2晚期的中心脱位和适当的主轴组件和忠实的染色体分离在有丝分裂中是必不可少的。 Gas2L1含有Calponin-同源性(CH)结构域和与F-Actin和Microtubels结合的钙醌 - 同源域和与GAR)结构域。值得注意的是,CH和GAR域彼此结合以抑制两个域的功能,并且Ser352磷酸化破坏了两个域之间的相互作用并缓解了自动抑制。我们解释了Gas2L1磷酸化和Centosome-Linker拆卸的作用,即另一个Nek2介导的事件,并且发现这些事件一起触发了Cientrosome分离。因此,我们的研究结果展示了将Centosomes在G2晚期分开的齐齐欲的NEK2动作。

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