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蓬乱蛋白激活JNK并区分平面极性和无翅信号通路中的JNK信号通路。

Dishevelled activates JNK and discriminates between JNK pathways in planar polarity and wingless signaling.

作者信息

Boutros M, Paricio N, Strutt D I, Mlodzik M

机构信息

European Molecular Biology Laboratory, Developmental Biology Programme, Heidelberg, Germany.

出版信息

Cell. 1998 Jul 10;94(1):109-18. doi: 10.1016/s0092-8674(00)81226-x.

Abstract

Frizzled family proteins have been described as receptors of Wnt signaling molecules. In Drosophila, the two known Frizzled proteins are associated with distinct developmental processes. Genesis of epithelial planar polarity requires Frizzled, whereas Dfz2 affects morphogenesis by wingless-mediated signaling. Dishevelled is required in both signaling pathways. Here, we use genetic and overexpression assays to show that Dishevelled activates JNK cascades. Rescue analysis reveals different protein domain requirements in Dishevelled for the two pathways; the C-terminal DEP domain is essential to rescue planar polarity defects and induce JNK signaling. Furthermore, the planar polarity-specific dsh1 allele is mutated in the DEP domain. Our results indicate that different Wnt/Fz signals activate distinct intracellular pathways, and Dishevelled discriminates among them by distinct domain interactions.

摘要

卷曲蛋白家族已被描述为Wnt信号分子的受体。在果蝇中,两种已知的卷曲蛋白与不同的发育过程相关。上皮平面极性的形成需要卷曲蛋白,而Dfz2则通过无翅介导的信号传导影响形态发生。两种信号通路都需要散乱蛋白。在这里,我们使用遗传和过表达分析表明,散乱蛋白激活JNK级联反应。拯救分析揭示了两种通路中散乱蛋白对不同蛋白质结构域的需求;C端DEP结构域对于拯救平面极性缺陷和诱导JNK信号至关重要。此外,平面极性特异性dsh1等位基因在DEP结构域中发生了突变。我们的结果表明,不同的Wnt/Fz信号激活不同的细胞内通路,而散乱蛋白通过不同的结构域相互作用对它们进行区分。

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