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首页> 外文期刊>Nature Communications >Actin remodelling factors control ciliogenesis by regulating YAP/TAZ activity and vesicle trafficking
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Actin remodelling factors control ciliogenesis by regulating YAP/TAZ activity and vesicle trafficking

机译:肌动蛋白重塑因子通过调节YAP / TAZ活性和囊泡运输来控制纤毛形成

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摘要

Primary cilia exert a profound impact on cell signalling and cell cycle progression. Recently, actin cytoskeleton destabilization has been recognized as a dominant inducer of ciliogenesis, but the exact mechanisms regulating ciliogenesis remain poorly understood. Here we show that the actin cytoskeleton remodelling controls ciliogenesis by regulating transcriptional coactivator YAP/TAZ as well as ciliary vesicle trafficking. Cytoplasmic retention of YAP/TAZ correlates with active ciliogenesis either in spatially confined cells or in cells treated with an actin filament destabilizer. Moreover, knockdown of YAP/TAZ is sufficient to induce ciliogenesis, whereas YAP/TAZ hyperactivation suppresses serum starvation-mediated ciliogenesis. We also identify actin remodelling factors LIMK2 and TESK1 as key players in the ciliogenesis control network in which YAP/TAZ and directional vesicle trafficking are integral components. Our work provides new insights for understanding the link between actin dynamics and ciliogenesis.
机译:原发纤毛对细胞信号传导和细胞周期进程产生深远影响。最近,肌动蛋白细胞骨架去稳定已被认为是纤毛发生的主要诱因,但调节纤毛发生的确切机制仍知之甚少。在这里,我们显示肌动蛋白细胞骨架重塑通过调节转录共激活因子YAP / TAZ以及睫状小泡运输来控制纤毛发生。 YAP / TAZ的细胞质保留与空间受限细胞或用肌动蛋白丝去稳定剂处理的细胞中的主动纤毛发生有关。此外,YAP / TAZ的敲低足以诱导纤毛发生,而YAP / TAZ过度活化会抑制血清饥饿介导的纤毛发生。我们还确定肌动蛋白重塑因子LIMK2和TESK1是纤毛形成控制网络中的关键角色,其中YAP / TAZ和定向囊泡运输是必不可少的组成部分。我们的工作为理解肌动蛋白动力学与纤毛发生之间的联系提供了新的见解。

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