Suppr超能文献

达绍斯蛋白和 Fat 协调抑制达绍斯蛋白-Dlish 近似复合物以控制生长。

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

机构信息

Department of Molecular Genetics and Cell Biology, University of Chicago, Chicago, IL, USA.

出版信息

J Cell Biol. 2024 Dec 2;223(12). doi: 10.1083/jcb.202406119. Epub 2024 Oct 7.

Abstract

Two protocadherins, Dachsous and Fat, regulate organ growth in Drosophila via the Hippo pathway. Dachsous and Fat 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 represses Warts. Dachsous is believed to promote growth by recruiting and stabilizing this complex, while Fat represses growth by promoting its degradation. Here, we examine the functional relationships between the intracellular domains of Dachsous and Fat and the core complex. While Dachsous promotes the accumulation of core complex proteins in puncta, it is not required for their assembly. Indeed, the core complex accumulates maximally in the absence of both Dachsous and Fat. Furthermore, Dachsous represses growth in the absence of Fat by removing the core complex from the junctional cortex. Fat similarly recruits core complex components but promotes their degradation. Our findings reveal that Dachsous and Fat coordinately constrain tissue growth by repressing the core complex.

摘要

两个原钙黏蛋白蛋白 Dachsous 和 Fat 通过 Hippo 通路调节果蝇器官的生长。Dachsous 和 Fat 通过异源结合调节由 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,在那里它抑制 Warts。Dachsous 被认为通过招募和稳定该复合物来促进生长,而 Fat 通过促进其降解来抑制生长。在这里,我们研究了 Dachsous 和 Fat 的细胞内结构域与核心复合物之间的功能关系。虽然 Dachsous 促进核心复合物蛋白在点状结构中的积累,但它不是它们组装所必需的。事实上,核心复合物在 Dachsous 和 Fat 缺失的情况下最大程度地积累。此外,Dachsous 通过将核心复合物从连接皮层中移除来在 Fat 缺失的情况下抑制生长。Fat 也募集核心复合物的成分,但促进其降解。我们的研究结果表明,Dachsous 和 Fat 通过抑制核心复合物来协调地限制组织生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39a5/11461286/2590414ebc3e/JCB_202406119_Fig2.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验