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

Eukaryotic Cell Pub Date : 2015-09-01 Epub Date: 2015-06-26 DOI:10.1128/EC.00083-15
Huiqing Hu, Yi Liu, Qing Zhou, Sara Siegel, Ziyin Li
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引用次数: 26

Abstract

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.

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布氏锥虫中心粒侧轮蛋白SAS-6是前基体生物发生和鞭毛组装所必需的。
真核生物的中心粒作为细胞的微管组织中心(MTOC)进行纺锤体组装,其生物发生需要一种进化上保守的蛋白SAS-6来组装中心粒车轮。布鲁氏锥虫是一种早期的分支原生动物,它以基体作为鞭毛生核的MTOC。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知之甚少。在这里,我们报道了布鲁氏T. SAS-6同源物TbSAS-6在整个细胞周期中定位于成熟基体和前基体。TbSAS-6的RNA干扰(RNAi)抑制了原基体的生物发生,破坏了鞭毛的组装,导致细胞分裂阻滞。令人惊讶的是,布鲁氏体中TbSAS-6的过表达也会损害前基体复制和鞭毛组装,这与人类中SAS-6的过表达相反,后者会产生多余的中心粒。此外,我们发现,消耗布鲁氏T. Polo-like kinase, TbPLK或抑制TbPLK活性并不能消除TbSAS-6在基底体的定位,这与动物中Polo-like kinase在将SAS-6募集到中心粒中的重要作用相反。总之,这些结果确定了TbSAS-6在前基体生物发生和鞭毛组装中的重要作用,并表明存在一种不依赖tbplk的途径来控制布鲁氏体的基体复制。
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来源期刊
Eukaryotic Cell
Eukaryotic Cell 生物-微生物学
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审稿时长
1 months
期刊介绍: Eukaryotic Cell (EC) focuses on eukaryotic microbiology and presents reports of basic research on simple eukaryotic microorganisms, such as yeasts, fungi, algae, protozoa, and social amoebae. The journal also covers viruses of these organisms and their organelles and their interactions with other living systems, where the focus is on the eukaryotic cell. Topics include: - Basic biology - Molecular and cellular biology - Mechanisms, and control, of developmental pathways - Structure and form inherent in basic biological processes - Cellular architecture - Metabolic physiology - Comparative genomics, biochemistry, and evolution - Population dynamics - Ecology
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