命运规范触发TEAD-YAP和NANOG的正反馈循环,促进着床前胚胎外胚层的形成。

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Development Pub Date : 2025-01-01 Epub Date: 2025-01-09 DOI:10.1242/dev.203091
Naoki Hirono, Masakazu Hashimoto, Hiromi Shimojo, Hiroshi Sasaki
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引用次数: 0

摘要

在着床前胚胎中,外胚层(EPI)的命运由内细胞团的NANOG和GATA6表达的分离控制。TEAD-YAP相互作用在EPI形成过程中被激活,并且是多能因子表达所必需的。这些事件在EPI形成过程中以类似的时间异步发生,它们之间的关系仍然难以捉摸。在这里,我们研究了NANOG-GATA6和TEAD-YAP之间的关系。YAP的核积累仅发生在epi指定的细胞中,并且NANOG和TEAD-YAP之间存在正反馈回路。在epi特异性细胞中,TEAD-YAP对SOX2上调的影响可能是间接的。EPI命运规格也改变了Nanog、Sox2和Cdx2对TEAD-YAP的反应。这些结果表明,EPI命运规范改变了转录网络从样森拉状态到EPI指定状态,并激活TEAD-YAP触发与NANOG的正反馈循环,从而稳定了EPI命运。这些过程在单个细胞中的协调发生可能支持在异步EPI命运规范条件下适当的EPI形成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fate specification triggers a positive feedback loop of TEAD-YAP and NANOG to promote epiblast formation in preimplantation embryos.

In preimplantation embryos, epiblast (EPI) fate specification from the inner cell mass is controlled by the segregation of NANOG and GATA6 expression. TEAD-YAP interaction is activated during EPI formation and is required for pluripotency factor expression. These events occur asynchronously with similar timing during EPI formation, and their relationship remains elusive. Here, we examined the relationship between NANOG-GATA6 and TEAD-YAP. The nuclear accumulation of YAP takes place only in EPI-specified cells, and a positive feedback loop operates between NANOG and TEAD-YAP. The effects of TEAD-YAP on SOX2 upregulation in EPI-specified cells are likely indirect. EPI fate specification also alters the response of Nanog, Sox2 and Cdx2 to TEAD-YAP. These results suggest that EPI-fate specification alters the transcriptional network from the morula-like to the EPI-specified state and activates TEAD-YAP to trigger a positive feedback loop with NANOG, which stabilizes the EPI fate. The coordinated occurrence of these processes in individual cells likely supports proper EPI formation under the condition of asynchronous EPI-fate specification.

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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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