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Regulation of Cell Polarity and Protrusion Formation by Targeting RhoA for Degradation

机译:通过靶向降解RhoA调节细胞极性和突起形成

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The Rho family of small guanosine triphosphatases regulates actin cytoskeleton dynamics that underlie cellular functions such as cell shape changes, migration, and polarity. We found that Smurf1, a HECT domain E3 ubiquitin ligase, regulated cell polarity and protrusive activity and was required to maintain the transformed morphology and motility of a tumor cell. Atypical protein kinase C zeta (PKCξ), an effector of the Cdc42/Rac1-PAR6 polarity complex, recruited Smurf1 to cellular protrusions, where it controlled the local level of RhoA. Smurf1 thus links the polarity complex to degradation of RhoA in lamellipodia and filopodia to prevent RhoA signaling during dynamic membrane movements.
机译:小鸟苷三磷酸酶的Rho家族调节肌动蛋白的细胞骨架动力学,这些动力学是细胞功能(如细胞形状变化,迁移和极性)的基础。我们发现Smurf1,HECT域E3泛素连接酶,调节细胞极性和突出活性,是维持肿瘤细胞转化形态和运动性所必需的。非典型蛋白激酶C zeta(PKCξ),Cdc42 / Rac1-PAR6极性复合物的效应物,将Smurf1募集到细胞突起处,在那里它控制RhoA的局部水平。因此,Smurf1将极性复合物与片状脂蛋白和丝状伪足中RhoA的降解联系起来,以防止动态膜运动过程中RhoA信号传导。

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