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达索蛋白和脂肪蛋白协同抑制达克斯-德利什-近似复合体以控制生长。

Dachsous and Fat coordinately repress the Dachs-Dlish-Approximated complex to control growth.

作者信息

Matakatsu Hitoshi, Fehon Richard G

出版信息

bioRxiv. 2024 Aug 28:2024.06.18.599638. doi: 10.1101/2024.06.18.599638.

Abstract

Two protocadherins, Dachsous (Ds) and Fat (Ft), regulate organ growth via the Hippo pathway. Ds and Ft bind heterotypically to regulate the abundance and subcellular localization of a 'core complex' consisting of Dachs, Dlish and Approximated. This complex localizes to the junctional cortex where it promotes growth by repressing the pathway kinase Warts. Ds is believed to promote growth by recruiting and stabilizing the core complex at the junctional cortex, while Ft represses growth by promoting degradation of core complex components. Here, we examine the functions of intracellular domains of Ds and Ft and their relationship to the core complex. While Ds promotes accumulation of the core complex proteins in cortical puncta, it is not required for core complex assembly. Indeed, the core complex assembles maximally in the absence of both Ds and Ft. Furthermore, while Ds promotes growth in the presence of Ft, it represses growth in the absence of Ft by removing the core complex from the junctional cortex. Ft similarly recruits core complex components, however it normally promotes their degradation. Our findings reveal that Ds and Ft constrain tissue growth by repressing the default 'on' state of the core complex.

摘要

两种原钙黏蛋白,Dachsous(Ds)和Fat(Ft),通过Hippo信号通路调节器官生长。Ds和Ft以异型方式结合,以调节由Dachs、Dlish和Approximated组成的“核心复合物”的丰度和亚细胞定位。该复合物定位于连接皮层,在那里通过抑制通路激酶Warts来促进生长。据信,Ds通过在连接皮层募集并稳定核心复合物来促进生长,而Ft则通过促进核心复合物成分的降解来抑制生长。在这里,我们研究了Ds和Ft的细胞内结构域的功能及其与核心复合物的关系。虽然Ds促进核心复合物蛋白在皮层点状结构中的积累,但它不是核心复合物组装所必需的。事实上,在没有Ds和Ft的情况下,核心复合物的组装达到最大程度。此外,虽然Ds在有Ft的情况下促进生长,但在没有Ft的情况下,它通过将核心复合物从连接皮层移除来抑制生长。Ft同样募集核心复合物成分,然而它通常促进它们的降解。我们的研究结果表明,Ds和Ft通过抑制核心复合物的默认“开启”状态来限制组织生长。

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