Prickle and Ror modulate Dishevelled-Vangl interaction to regulate non-canonical Wnt signaling during convergent extension.

Hwa-Seon Seo, Deli Yu, Ivan Popov, Jiahui Tao, Allyson Angermeier, Fei Yang, Sylvie Marchetto, Jean-Paul Borg, Bingdong Sha, Jeffrey D Axelrod, Chenbei Chang, Jianbo Wang
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Abstract

Convergent extension (CE) is a fundamental morphogenetic process where oriented cell behaviors lead to polarized extension of diverse tissues. In vertebrates, regulation of CE requires both non-canonical Wnt, its co-receptor Ror, and several "core members" of the planar cell polarity (PCP) pathway. PCP was originally identified as a mechanism to coordinate the cellular polarity in the plane of static epithelium, where core proteins Frizzled (Fz)/ Dishevelled (Dvl) and Van Gogh-like (Vangl)/ Prickle (Pk) partition to opposing cell cortex. But how core PCP proteins interact with each other to mediate non-canonical Wnt/ Ror signaling during CE is not clear. We found previously that during CE, Vangl cell-autonomously recruits Dvl to the plasma membrane and keeps Dvl inactive. In this study, we show that non-canonical Wnt induces Dvl to transition from Vangl to Fz. Pk inhibits the transition, and functionally synergize with Vangl to suppress Dvl during CE. Conversely, Ror is required for the transition, and functionally antagonizes Vangl. Biochemically, Vangl interacts directly with both Ror and Dvl. Ror and Dvl do not bind directly, but can be cofractionated with Vangl. Collectively, we propose that Pk assists Vangl to function as an unconventional adaptor that brings Dvl and Ror into a complex to serves two functions: 1) simultaneously preventing both Dvl and Ror from ectopically activating non-canonical Wnt signaling; and 2) relaying Dvl to Fz for signaling activation upon non-canonical Wnt induced dimerization of Fz and Ror.

Prickle和Ror在会聚延伸过程中调节Dishevelled Vangl相互作用以调节非规范Wnt信号传导。
会聚延伸(CE)是一个基本的形态发生过程,定向细胞行为导致不同组织的极化延伸。在脊椎动物中,CE的调节需要非经典Wnt、其共受体Ror和平面细胞极性(PCP)途径的“核心成员”。PCP最初被认为是一种在静止上皮平面内协调细胞极性的机制,其中核心蛋白Frizzled(Fz)/Dischevelled(Dvl)和Van Gogh样(Vangl)/Prickel(Pk)分配到相对的细胞皮层。但核心PCP蛋白如何在CE期间相互作用以介导非经典Wnt/Ror信号传导尚不清楚。我们之前发现,在CE期间,Vangl细胞自主地将Dvl募集到质膜,但同时保持Dvl不活跃。在本研究中,我们发现非正则Wnt诱导Dvl从Vangl向Fz转变。PK抑制这种转变,并在CE过程中与Vangl协同抑制Dvl。相反,Ror是过渡所必需的,并且在功能上拮抗Vangl。在生物化学上,Vangl与Ror和Dvl直接相互作用。Ror和Dvl不直接结合,但可以与Vangl共分馏。我们提出,Pk帮助Vangl作为一种非常规的衔接子发挥作用,将Dvl和Ror带入一个复合体中,发挥两种功能:1)同时防止Dvl或Ror异位激活非规范Wnt信号;和2)在非规范Wnt诱导的Fz和Ror的二聚化时,将Dvl中继到Fz用于信号激活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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