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smoothened 通过与 Evc/Evc2 形成复合物来转导 Hedgehog 信号。

Smoothened transduces Hedgehog signal by forming a complex with Evc/Evc2.

机构信息

Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences and Yunnan Province, Kunming Institute of Zoology, Chinese Academy of Sciences, 32 Jiaochang Donglu, Kunming, Yunnan 650223, China.

出版信息

Cell Res. 2012 Nov;22(11):1593-604. doi: 10.1038/cr.2012.134. Epub 2012 Sep 18.

Abstract

Hedgehog (Hh) signaling plays pivotal roles in embryonic development and adult tissue homeostasis in species ranging from Drosophila to mammals. The Hh signal is transduced by Smoothened (Smo), a seven-transmembrane protein related to G protein coupled receptors. Despite a conserved mechanism by which Hh activates Smo in Drosophila and mammals, how mammalian Hh signal is transduced from Smo to the Gli transcription factors is poorly understood. Here, we provide evidence that two ciliary proteins, Evc and Evc2, the products of human disease genes responsible for the Ellis-van Creveld syndrome, act downstream of Smo to transduce the Hh signal. We found that loss of Evc/Evc2 does not affect Sonic Hedgehog-induced Smo phosphorylation and ciliary localization but impedes Hh pathway activation mediated by constitutively active forms of Smo. Evc/Evc2 are dispensable for the constitutive Gli activity in Sufu(-/-) cells, suggesting that Evc/Evc2 act upstream of Sufu to promote Gli activation. Furthermore, we demonstrated that Hh stimulates binding of Evc/Evc2 to Smo depending on phosphorylation of the Smo C-terminal intracellular tail and that the binding is abolished in Kif3a(-/-) cilium-deficient cells. We propose that Hh activates Smo by inducing its phosphorylation, which recruits Evc/Evc2 to activate Gli proteins by antagonizing Sufu in the primary cilia.

摘要

刺猬 (Hh) 信号在从果蝇到哺乳动物等物种的胚胎发育和成年组织稳态中发挥着关键作用。Hh 信号由 Smoothened (Smo) 转导,Smoothened 是一种与 G 蛋白偶联受体相关的七跨膜蛋白。尽管 Hh 在果蝇和哺乳动物中激活 Smo 的机制是保守的,但哺乳动物 Hh 信号如何从 Smo 转导到 Gli 转录因子尚不清楚。在这里,我们提供的证据表明,两种纤毛蛋白 Evc 和 Evc2 是人类疾病基因的产物,这些基因负责 Ellis-van Creveld 综合征,它们在 Smo 下游转导 Hh 信号。我们发现,Evc/Evc2 的缺失不影响 Sonic Hedgehog 诱导的 Smo 磷酸化和纤毛定位,但阻碍了由 Smo 组成性激活形式介导的 Hh 通路激活。Evc/Evc2 对于 Sufu(-/-) 细胞中的组成性 Gli 活性是可有可无的,这表明 Evc/Evc2 在 Sufu 上游起作用以促进 Gli 激活。此外,我们证明 Hh 刺激 Evc/Evc2 与 Smo 的结合取决于 Smo 胞内 C 端尾部的磷酸化,并且在 Kif3a(-/-)纤毛缺陷细胞中这种结合被消除。我们提出 Hh 通过诱导其磷酸化来激活 Smo,磷酸化的 Smo 招募 Evc/Evc2 到初级纤毛中,通过拮抗 Sufu 来激活 Gli 蛋白。

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本文引用的文献

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