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The Centriole Cartwheel Protein SAS-6 in Trypanosoma brucei Is Required for Probasal Body Biogenesis and Flagellum Assembly

机译:布鲁氏锥虫中的中心车轮蛋白SAS-6是基础体生物发生和鞭毛组装所必需的

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摘要

The centriole in eukaryotes functions as the cell's microtubule-organizing center (MTOC) to nucleate spindle assembly, and its biogenesis requires an evolutionarily conserved protein, SAS-6, which assembles the centriole cartwheel. Trypanosoma brucei, an early branching protozoan, possesses the basal body as its MTOC to nucleate flagellum biogenesis. However, little is known about the components of the basal body and their roles in basal body biogenesis and flagellum assembly. Here, we report that the T. brucei SAS-6 homolog, TbSAS-6, is localized to the mature basal body and the probasal body throughout the cell cycle. RNA interference (RNAi) of TbSAS-6 inhibited probasal body biogenesis, compromised flagellum assembly, and caused cytokinesis arrest. Surprisingly, overexpression of TbSAS-6 in T. brucei also impaired probasal body duplication and flagellum assembly, contrary to SAS-6 overexpression in humans, which produces supernumerary centrioles. Furthermore, we showed that depletion of T. brucei Polo-like kinase, TbPLK, or inhibition of TbPLK activity did not abolish TbSAS-6 localization to the basal body, in contrast to the essential role of Polo-like kinase in recruiting SAS-6 to centrioles in animals. Altogether, these results identified the essential role of TbSAS-6 in probasal body biogenesis and flagellum assembly and suggest the presence of a TbPLK-independent pathway governing basal body duplication in T. brucei.
机译:真核生物中的中心粒充当细胞的微管组织中心(MTOC)以使纺锤体组装成核,并且其生物发生需要进化上保守的蛋白质SAS-6,该蛋白组装了中心粒车轮。布鲁氏锥虫(Trypanosoma brucei)是早期的原生动物,具有基底体作为其MTOC来使鞭毛生物发生成核。然而,人们对基体的组成及其在基体生物发生和鞭毛组装中的作用了解甚少。在这里,我们报告T.布鲁西SAS-6同源物,TbSAS-6,在整个细胞周期中都定位于成熟的基体和前基体。 TbSAS-6的RNA干扰(RNAi)抑制了基底体的生物发生,鞭毛组装受损并引起胞质分裂阻滞。出乎意料的是,与人中产生多余数目中心粒的SAS-6过量表达相反,在布鲁氏菌中过表达TbSAS-6也会损害基体复制和鞭毛组装。此外,我们发现,布鲁氏菌Polo样激酶,TbPLK的耗竭或TbPLK活性的抑制作用不会消除TbSAS-6定位于基体的作用,这与Polo样激酶在招募SAS-6方面的基本作用相反到动物的中心粒。总而言之,这些结果确定了TbSAS-6在基体生物发生和鞭毛组装中的重要作用,并暗示了在T. brucei中存在一种不依赖TbPLK的途径来控制基体重复。

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