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首页> 外文期刊>Cell cycle >A centrosomal protein STARD9 promotes microtubule stability and regulates spindle microtubule dynamics
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A centrosomal protein STARD9 promotes microtubule stability and regulates spindle microtubule dynamics

机译:Centrosomal蛋白质Stard9促进微管稳定性并调节主轴微管动态

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摘要

Centrosomal proteins play important roles in the spindle assembly and the segregation of chromosomes in the eukaryotic cells. STARD9, a recently identified centrosomal protein, was reported to influence the spindle pole assembly. However, the role of STARD9 in maintaining the stability and organization of microtubules are not known. Here, we show that STARD9 regulates the assembly and dynamics of both interphase and mitotic microtubules. The knockdown of STARD9 in HeLa or HCT116 cells with siRNA or shRNA induced a strong depolymerization of the interphase microtubules. The over-expression of the motor domain of STARD9 stabilizes microtubules against cold and nocodazole suggesting that STARD9 stabilizes microtubules in HeLa cells. Using fluorescent recovery after photobleaching, we showed that the knockdown of STARD9 strongly reduced microtubule dynamics in the live spindles of HeLa cells. The reassembly of microtubules in the STARD9-depleted cells was strongly reduced as compared to the microtubules in the control cells implying the role of STARD9 in the nucleation of microtubules. Further, the depletion of STARD9 inhibited chromosome separation and the STARD9-depleted HeLa cells were blocked at mitosis. Interestingly, the frequency of multipolar spindle formation increased significantly in the STARD9-depleted HeLa cells in the presence of vinblastine and the STARD9-depleted cells showed much higher sensitivity towards vinblastine than the control cells indicating a new approach for cancer chemotherapy. The evidence suggests that STARD9 regulates the assembly and stability of both interphase and spindle microtubules and thereby, play important roles in the cell cycle progression.
机译:CentroSomal蛋白在主轴组件中起重要作用和真核细胞中染色体的分离。据报道,STARD9,最近确定的Centrosomal蛋白,以影响主轴杆组件。然而,Stard9在保持稳定性和组织微管中的作用是不知道的。在这里,我们表明Stard9调节了间间和有丝分裂微管的组装和动态。 STARD9在HELA或HCT116细胞中的敲低,SiRNA或shRNA诱导了对间间微管的强脱色。 STARD9的电动机结构域的过表达稳定了对寒冷和Nocodazole的微管,这表明Stard9稳定了HeLa细胞中的微管。光博后使用荧光恢复,我们表明Stard9的敲低在Hela细胞的活纺织中强烈降低了微管动态。与对照细胞中的微管相比,在对照细胞中的微管中暗示了STARD9在微管核成核中的作用相比,在STARD9耗尽细胞中的微管重组被强烈降低。此外,Stard9的耗竭抑制染色体分离,并且在有丝分裂下阻断了Stard9耗尽的Hela细胞。有趣的是,在菌状物的存在下,在心脏病9耗尽的Hela细胞中,多极纺锤体形成的频率显着增加,并且Stard9耗尽的细胞对导致血管线的敏感性远远高于指示癌症化疗的新方法的控制细胞。证据表明,Stard9调节了相互作用和主轴微管的组装和稳定性,从而在细胞周期进展中起重要作用。

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