Canonical Wnt signalling from the area opaca induces and maintains the marginal zone in pre-primitive-streak stage chick embryos.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Development Pub Date : 2025-01-15 Epub Date: 2025-01-23 DOI:10.1242/dev.204350
Yara Fadaili, Hui-Chun Lu, Hyung Chul Lee, Amra Ryazapova, Claudio D Stern
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Abstract

In chick embryos before primitive streak formation, the outermost extra-embryonic region, known as the area opaca (AO), was generally thought to act only by providing nutrients and mechanical support to the embryo. Immediately internal to the AO is a ring of epiblast called the marginal zone (MZ), separating the former from the inner area pellucida (AP) epiblast. The MZ does not contribute cells to any part of the embryo but is involved in determining the position of primitive streak formation from the adjacent AP epiblast. Recently, it was discovered that the AO can induce an MZ from AP epiblast. Here, we explore the nature of this inductive signal. We find that WNT8C is highly expressed in the AO, whereas canonical Wnt pathway targets are enriched in the MZ, along with strong nuclear β-catenin localization. Using isolation and recombination experiments combined with gain- and loss-of-function by exogenous chemical modulators of the pathway, we reveal that Wnt signalling is essential for induction and maintenance of the MZ, as well as sufficient to induce MZ properties in AP epiblast. We propose that canonical Wnt signalling is responsible for induction of the MZ by the area opaca.

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来自不透明区的典型Wnt信号在原始条纹期前的鸡胚胎中诱导和维持边缘区。
在原始条纹形成之前的小鸡胚胎中,最外层的胚胎外区域,即不透明区域(AO),通常被认为仅为胚胎提供营养和机械支持。AO的内部是一圈外胚层,称为边缘带(MZ),将前者与内部透明外胚层区分开。MZ不向胚胎的任何部分提供细胞,但参与确定从邻近区域透明外胚层形成原始条纹的位置。近年来发现AO能诱导透明外胚层发生MZ。在这里,我们探讨这种感应信号的性质。我们发现WNT8C在AO中高度表达,而典型的Wnt通路靶点在MZ中富集,并且具有强的核β-catenin定位。通过分离和重组实验,结合外源性化学调节剂的功能增益和功能损失,我们发现Wnt信号对于诱导和维持MZ至关重要,并且足以诱导透明外胚层的MZ特性。我们认为典型的Wnt信号是不透明区域诱导边缘区的原因。
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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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