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Tomoregulin-1 (TMEFF1) inhibits nodal signaling through direct binding to the nodal coreceptor Cripto

机译:Tomoregulin-1(TMEFF1)通过直接结合节点共同受体Cripto抑制节点信号传导

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摘要

Transforming growth factor β (TGF-β) signals regulate multiple processes during development and in adult. We recently showed that tomoregulin-1 (TMEFF1), a transmembrane protein, selectively inhibits nodal but not activin in early Xenopus embryos. Here we report that TMEFF1 binds to the nodal coreceptor Cripto, but does not associate with either nodal or the type I ALK (activin receptor-like kinase) 4 receptor in coimmunoprecipitation assays. The inhibition of the nodal signaling by TMEFF1 in Xenopus ectodermal explants is rescued with wild-type but not mutant forms of Cripto. Furthermore, we show that the Cripto-FRL1-Cryptic (CFC) domain in Cripto, which is essential for its binding to ALK4, is also important for its interaction with TMEFF1. Our results demonstrate for the first time that nodal signaling can be regulated by a novel mechanism of blocking the Cripto coreceptor.
机译:转化生长因子β(TGF-β)信号调节发育过程中和成年期的多个过程。我们最近显示,tomoregulin-1(TMEFF1),一种跨膜蛋白,选择性地抑制非洲爪蟾早期胚胎中的淋巴结但不抑制激活素。在这里,我们报告TMEFF1绑定到节点共受体Cripto,但在联合免疫沉淀测定中不与节点或I型ALK(激活素受体样激酶)4受体结合。用野生型而非突变型的Cripto挽救非洲爪蟾外胚层外植体中TMEFF1对节点信号的抑制作用。此外,我们显示Cripto中的Cripto-FRL1-Cryptic(CFC)域对于绑定到ALK4是必不可少的,对于与TMEFF1的交互作用也很重要。我们的结果首次证明,可以通过阻断Cripto共受体的新机制来调节淋巴结信号。

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