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首页> 外文期刊>Nature Communications >The clathrin adaptor AP-1 complex and Arf1 regulate planar cell polarity in vivo
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The clathrin adaptor AP-1 complex and Arf1 regulate planar cell polarity in vivo

机译:网格蛋白适配器AP-1复合物和Arf1在体内调节平面细胞极性

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摘要

A key step in generating planar cell polarity (PCP) is the formation of restricted junctional domains containing Frizzled/Dishevelled/Diego (Fz/Dsh/Dgo) or Van Gogh/Prickle (Vang/Pk) complexes within the same cell, stabilized via Flamingo (Fmi) across cell membranes. Although models have been proposed for how these complexes acquire and maintain their polarized localization, the machinery involved in moving core PCP proteins around cells remains unknown. We describe the AP-1 adaptor complex and Arf1 as major regulators of PCP protein trafficking in vivo. AP-1 and Arf1 disruption affects the accumulation of Fz/Fmi and Vang/Fmi complexes in the proximo-distal axis, producing severe PCP phenotypes. Using novel tools, we demonstrate a direct and specific Arf1 involvement in Fz trafficking in vivo. Moreover, we uncover a conserved Arf1 PCP function in vertebrates. Our data support a model whereby the trafficking machinery plays an important part during PCP establishment, promoting formation of polarized PCP-core complexes in vivo.
机译:产生平面细胞极性(PCP)的关键步骤是在同一细胞内形成受限的连接域,其中包含卷曲,分散/迭戈(Fz / Dsh / Dgo)或梵高/皮刺(Vang / Pk)复合物,并通过火烈鸟使其稳定(Fmi)跨细胞膜。尽管已经提出了关于这些复合物如何获得和维持其极化定位的模型,但是涉及在细胞周围移动核心PCP蛋白的机制仍然未知。我们将AP-1适配器复合体和Arf1描述为体内PCP蛋白运输的主要调节剂。 AP-1和Arf1的破坏会影响Fz / Fmi和Vang / Fmi复合物在近距轴上的积累,产生严重的PCP表型。使用新颖的工具,我们证明了Ff在体内直接和特定Arf1参与贩运。此外,我们发现脊椎动物中保守的Arf1 PCP功能。我们的数据支持了一种模型,在该模型中,贩运机制在五氯苯酚建立过程中起着重要的作用,促进了体内极化的五氯苯酚核心复合物的形成。

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