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棘蛋白和Ror调节Dishevelled与Vangl的相互作用,以在汇聚延伸过程中调控非经典Wnt信号通路。

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

作者信息

Seo Hwa-Seon, Yu Deli, Popov Ivan, Tao Jiahui, Angermeier Allyson, Sha Bingdong, Axelrod Jeffrey D, Chang Chenbei, Wang Jianbo

出版信息

bioRxiv. 2023 Sep 30:2023.08.29.555374. doi: 10.1101/2023.08.29.555374.

DOI:10.1101/2023.08.29.555374
PMID:37693429
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10491138/
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 "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)/ Prickel (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 but simultaneously 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. 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.

摘要

汇聚延伸(CE)是一种基本的形态发生过程,在此过程中,定向的细胞行为导致多种组织的极化延伸。在脊椎动物中,CE的调节需要非经典Wnt、其共受体Ror以及平面细胞极性(PCP)途径的“核心成员”。PCP最初被确定为一种在静态上皮平面中协调细胞极性的机制,其中核心蛋白卷曲蛋白(Fz)/ 散乱蛋白(Dvl)和类梵高蛋白(Vangl)/ 刺突蛋白(Pk)分别定位于相对的细胞皮质。但是,在CE过程中,核心PCP蛋白如何相互作用以介导非经典Wnt / Ror信号尚不清楚。我们先前发现,在CE过程中,Vangl在细胞自主的情况下将Dvl募集到质膜,但同时使Dvl保持无活性。在本研究中,我们表明非经典Wnt诱导Dvl从Vangl转变为Fz。PK抑制这种转变,并在功能上与Vangl协同作用以在CE过程中抑制Dvl。相反,Ror是这种转变所必需的,并且在功能上拮抗Vangl。在生化方面,Vangl直接与Ror和Dvl相互作用。Ror和Dvl不直接结合,但可以与Vangl一起分级分离。我们提出,Pk协助Vangl充当一种非常规接头,将Dvl和Ror带入一个复合物中,以发挥两种功能:1)同时防止Dvl和Ror异位激活非经典Wnt信号;2)在非经典Wnt诱导Fz和Ror二聚化时,将Dvl传递给Fz以激活信号。