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Tank binding kinase 1 is a centrosome-associated kinase necessary for microtubule dynamics and mitosis

机译:储罐结合激酶1是微管动力学和有丝分裂所必需的与中心体相关的激酶

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TANK Binding Kinase 1 (TBK1) is a non-canonical I kappa B kinase that contributes to KRAS-driven lung cancer. Here we report that TBK1 plays essential roles in mammalian cell division. Specifically, levels of active phospho-TBK1 increase during mitosis and localize to centrosomes, mitotic spindles and midbody, and selective inhibition or silencing of TBK1 triggers defects in spindle assembly and prevents mitotic progression. TBK1 binds to the centrosomal protein CEP170 and to the mitotic apparatus protein NuMA, and both CEP170 and NuMA are TBK1 substrates. Further, TBK1 is necessary for CEP170 centrosomal localization and binding to the microtubule depolymerase Kif2b, and for NuMA binding to dynein. Finally, selective disruption of the TBK1-CEP170 complex augments microtubule stability and triggers defects in mitosis, suggesting that TBK1 functions as a mitotic kinase necessary for microtubule dynamics and mitosis.
机译:TANK结合激酶1(TBK1)是一种非经典的IκB激酶,可导致KRAS驱动的肺癌。在这里,我们报告TBK1在哺乳动物细胞分裂中发挥重要作用。具体而言,活性磷酸-TBK1的水平在有丝分裂期间增加,并定位于中心体,有丝分裂纺锤体和中体,并且选择性抑制或沉默TBK1会触发纺锤体装配中的缺陷并阻止有丝分裂进程。 TBK1与中心体蛋白CEP170和有丝分裂器蛋白NuMA结合,而CEP170和NuMA都是TBK1底物。此外,TBK1对于CEP170中心体定位和与微管解聚酶Kif2b的结合以及对于NuMA与动力蛋白的结合是必需的。最后,对TBK1-CEP170复合物的选择性破坏会增强微管的稳定性,并引发有丝分裂的缺陷,这表明TBK1充当了微管动力学和有丝分裂所必需的有丝分裂激酶。

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