肿瘤调节蛋白-1(TMEFF1)通过直接结合结节共受体Cripto来抑制结节信号传导。

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

作者信息

Harms Paul W, Chang Chenbei

机构信息

Department of Cell Biology, The University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.

出版信息

Genes Dev. 2003 Nov 1;17(21):2624-9. doi: 10.1101/gad.1127703. Epub 2003 Oct 16.

Abstract

Transforming growth factor beta (TGF-beta) 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.

摘要

转化生长因子β(TGF-β)信号在发育过程和成年期调节多种过程。我们最近发现,跨膜蛋白tomoregulin-1(TMEFF1)在非洲爪蟾早期胚胎中选择性抑制节点信号而非激活素信号。在此我们报告,TMEFF1与节点共受体Cripto结合,但在免疫共沉淀实验中不与节点或I型激活素受体样激酶(ALK)4受体结合。用野生型而非突变型Cripto可挽救TMEFF1在非洲爪蟾外胚层外植体中对节点信号的抑制作用。此外,我们表明,Cripto中对其与ALK4结合至关重要的Cripto-FRL1-Cryptic(CFC)结构域,对其与TMEFF1的相互作用也很重要。我们的结果首次证明,节点信号可通过一种阻断Cripto共受体的新机制进行调节。

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