首页> 美国卫生研究院文献>EvoDevo >A novel gene’s role in an ancient mechanism: secreted Frizzled-related protein 1 is a critical component in the anterior–posterior Wnt signaling network that governs the establishment of the anterior neuroectoderm in sea urchin embryos
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A novel gene’s role in an ancient mechanism: secreted Frizzled-related protein 1 is a critical component in the anterior–posterior Wnt signaling network that governs the establishment of the anterior neuroectoderm in sea urchin embryos

机译:一种新基因在古老机制中的作用:分泌的卷曲蛋白相关蛋白1是控制海胆胚胎前神经外胚层建立的前后Wnt信号网络的关键组成部分

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摘要

The anterior neuroectoderm (ANE) in many deuterostome embryos (echinoderms, hemichordates, urochordates, cephalochordates, and vertebrates) is progressively restricted along the anterior–posterior axis to a domain around the anterior pole. In the sea urchin embryo, three integrated Wnt signaling branches (Wnt/β-catenin, Wnt/JNK, and Wnt/PKC) govern this progressive restriction process, which begins around the 32- to 60-cell stage and terminates by the early gastrula stage. We previously have established that several secreted Wnt modulators of the Dickkopf and secreted Frizzled-related protein families (Dkk1, Dkk3, and sFRP-1/5) are expressed within the ANE and play important roles in modulating the Wnt signaling network during this process. In this study, we use morpholino and dominant-negative interference approaches to characterize the function of a novel Frizzled-related protein, secreted Frizzled-related protein 1 (sFRP-1), during ANE restriction. sFRP-1 appears to be related to a secreted Wnt modulator, sFRP3/4, that is essential to block Wnt signaling and establish the ANE in vertebrates. Here, we show that the sea urchin sFRP3/4 orthologue is not expressed during ANE restriction in the sea urchin embryo. Instead, our results indicate that ubiquitously expressed maternal sFRP-1 and Fzl1/2/7 signaling act together as early as the 32- to 60-cell stage to antagonize the ANE restriction mechanism mediated by Wnt/β-catenin and Wnt/JNK signaling. Then, starting from the blastula stage, Fzl5/8 signaling activates zygotic sFRP-1 within the ANE territory, where it works with the secreted Wnt antagonist Dkk1 (also activated by Fzl5/8 signaling) to antagonize Wnt1/Wnt8–Fzl5/8–JNK signaling in a negative feedback mechanism that defines the outer ANE territory boundary. Together, these data indicate that maternal and zygotic sFRP-1 protects the ANE territory by antagonizing the Wnt1/Wnt8–Fzl5/8–JNK signaling pathway throughout ANE restriction, providing precise spatiotemporal control of the mechanism responsible for the establishment of the ANE territory around the anterior pole of the sea urchin embryo.Electronic supplementary materialThe online version of this article (10.1186/s13227-017-0089-3) contains supplementary material, which is available to authorized users.
机译:在许多氘核胚胎(棘皮动物,半甲酸盐,泌尿针,头针和脊椎动物)中,前神经外胚层(ANE)沿前后轴逐渐限制在前极周围。在海胆胚胎中,三个整合的Wnt信号分支(Wnt /β-catenin,Wnt / JNK和Wnt / PKC)控制着这种渐进的限制性过程,该过程开始于32至60细胞阶段,并终止于早期胃阶段。我们先前已经确定,Dickkopf的几种分泌型Wnt调节剂和卷曲的相关蛋白家族的分泌物(Dkk1,Dkk3和sFRP-1 / 5)在ANE中表达,并在此过程中对Wnt信号网络的调节起重要作用。在这项研究中,我们使用吗啉代和显性-负性干扰方法来表征在ANE限制过程中一种新型的卷曲相关蛋白,分泌的卷曲相关蛋白1(sFRP-1)的功能。 sFRP-1似乎与分泌的Wnt调节剂sFRP3 / 4有关,这对于阻断Wnt信号传导并在脊椎动物中建立ANE至关重要。在这里,我们显示海胆sFRP3 / 4直向同源物在ANE限制中未在海胆胚胎中表达。相反,我们的结果表明,广泛表达的母体sFRP-1和Fzl1 / 2/7信号最早在32至60细胞阶段共同起作用,以拮抗Wnt /β-catenin和Wnt / JNK信号传导介导的ANE限制机制。 。然后,从囊胚阶段开始,Fzl5 / 8信号传导激活ANE区域内的合子sFRP-1,与分泌的Wnt拮抗剂Dkk1(也由Fzl5 / 8信号传导激活)共同拮抗Wnt1 / Wnt8–Fzl5 / 8–定义外部ANE区域边界的负反馈机制中的JNK信号。总之,这些数据表明,母体和合子sFRP-1通过在整个ANE限制期间拮抗Wnt1 / Wnt8–Fzl5 / 8–JNK信号通路来保护ANE领土,从而提供了对造成ANE领土周围机制负责的机制的精确时空控制电子补充材料本文的在线版本(10.1186 / s13227-017-0089-3)包含补充材料,授权用户可以使用。

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