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在间充质到上皮样转变过程中,elmo-mbc复合物和rhogap19d与Rho家族小GTP酶偶联。

The elmo-mbc complex and rhogap19d couple Rho family GTPases during mesenchymal-to-epithelial-like transitions.

作者信息

Toret Christopher P, Shivakumar Pruthvi C, Lenne Pierre-François, Le Bivic Andre

机构信息

Aix-Marseille Univ, CNRS, IBDM, Case 907, 13288 Marseille, Cedex 09, France

Aix-Marseille Univ, CNRS, IBDM, Case 907, 13288 Marseille, Cedex 09, France.

出版信息

Development. 2018 Feb 2. doi: 10.1242/dev.157495.

Abstract

Many metazoan developmental processes require cells to transition between migratory mesenchymal- and adherent epithelial-like states. These transitions require Rho GTPase-mediated actin rearrangements downstream of integrin and cadherin pathways. A regulatory toolbox of GEF and GAP proteins precisely coordinates Rho protein activities, yet defining the involvement of specific regulators within a cellular context remains a challenge due to overlapping and coupled activities. Here we demonstrate that dorsal closure is a powerful model for Rho GTPase regulation during transitions from leading edges to cadherin contacts. During these transitions a Rac GEF elmo-mbc complex regulates both lamellipodia and Rho1-dependent, actomyosin-mediated tension at initial cadherin contacts. Moreover, the Rho GAP Rhogap19d controls Rac and Rho GTPases during the same processes and genetically regulates the elmo-mbc complex. This study presents a fresh framework to understand the inter-relationship between GEF and GAP proteins that tether Rac and Rho cycles during developmental processes.

摘要

许多后生动物的发育过程需要细胞在迁移性间充质样状态和粘附性上皮样状态之间转换。这些转换需要整合素和钙粘蛋白途径下游的Rho GTP酶介导的肌动蛋白重排。GEF和GAP蛋白的调控工具箱精确地协调Rho蛋白的活性,然而,由于活动的重叠和耦合,在细胞环境中确定特定调控因子的参与仍然是一个挑战。在这里,我们证明背侧闭合是Rho GTP酶在从前缘到钙粘蛋白接触的转变过程中调控的一个有力模型。在这些转变过程中,一个Rac GEF elmo-mbc复合物在初始钙粘蛋白接触时调节片状伪足和Rho1依赖的、肌动球蛋白介导的张力。此外,Rho GAP Rhogap19d在相同过程中控制Rac和Rho GTP酶,并在基因上调节elmo-mbc复合物。这项研究提出了一个新的框架,以理解在发育过程中连接Rac和Rho循环的GEF和GAP蛋白之间的相互关系。

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