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辅助蛋白动态地重新平衡收缩力和伸出力以控制组织形态发生。

Sidekick dynamically rebalances contractile and protrusive forces to control tissue morphogenesis.

机构信息

Department of Developmental, Molecular & Chemical Biology, Program in Cell, Molecular and Developmental Biology and Program in Genetics, Tufts University School of Medicine, Boston, MA.

Skirball Institute for Biomolecular Medicine, New York, NY.

出版信息

J Cell Biol. 2022 May 2;221(5). doi: 10.1083/jcb.202107035. Epub 2022 Mar 8.

Abstract

Contractile actomyosin and protrusive branched F-actin networks interact in a dynamic balance, repeatedly contracting and expanding apical cell contacts to organize the epithelium of the developing fly retina. Previously we showed that the immunoglobulin superfamily protein Sidekick (Sdk) contributes to contraction by recruiting the actin binding protein Polychaetoid (Pyd) to vertices. Here we show that as tension increases during contraction, Sdk progressively accumulates at vertices, where it toggles to recruit the WAVE regulatory complex (WRC) to promote actin branching and protrusion. Sdk alternately interacts with the WRC and Pyd using the same C-terminal motif. With increasing protrusion, levels of Sdk and the WRC decrease at vertices while levels of Pyd increase paving the way for another round of contraction. Thus, by virtue of dynamic association with vertices and interchangeable associations with contractile and protrusive effectors, Sdk is central to controlling the balance between contraction and expansion that shapes this epithelium.

摘要

收缩性肌动球蛋白和伸出的分支丝状肌动蛋白网络相互作用处于动态平衡中,反复收缩和扩展顶端细胞接触,以组织发育中的果蝇视网膜的上皮。我们之前表明,免疫球蛋白超家族蛋白 Sidekick(Sdk)通过将肌动蛋白结合蛋白 Polychaetoid(Pyd)招募到顶点来促进收缩。在这里,我们表明在收缩过程中张力增加时,Sdk 逐渐积累在顶点处,在此处它切换以招募 WAVE 调节复合物(WRC)来促进肌动蛋白分支和伸出。Sdk 使用相同的 C 末端基序交替与 WRC 和 Pyd 相互作用。随着突起的增加,Sdk 和 WRC 的水平在顶点处降低,而 Pyd 的水平升高,为下一轮收缩铺平了道路。因此,通过与顶点的动态关联以及与收缩和伸出效应器的可互换关联,Sdk 是控制塑造该上皮细胞的收缩和扩张之间平衡的核心。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b18d/8908789/2c943e6df024/JCB_202107035_Fig1.jpg

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