Hirono Naoki, Hashimoto Masakazu, Shimojo Hiromi, Sasaki Hiroshi
Laboratory for Embryogenesis, Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka 565-0871, Japan.
Japan Science and Technology Agency, PRESTO, Kawaguchi, Saitama 332-0012, Japan.
Development. 2025 Jan 1;152(1). doi: 10.1242/dev.203091. Epub 2025 Jan 9.
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.
在植入前胚胎中,内细胞团向胚外外胚层(EPI)的命运特化由NANOG和GATA6表达的分离所控制。在EPI形成过程中,TEAD-YAP相互作用被激活,并且对于多能性因子的表达是必需的。这些事件在EPI形成过程中以相似的时间异步发生,它们之间的关系仍然难以捉摸。在这里,我们研究了NANOG-GATA6与TEAD-YAP之间的关系。YAP的核积累仅发生在指定为EPI的细胞中,并且在NANOG和TEAD-YAP之间存在正反馈回路。TEAD-YAP对指定为EPI的细胞中SOX2上调的影响可能是间接的。EPI命运特化也改变了Nanog、Sox2和Cdx2对TEAD-YAP的反应。这些结果表明,EPI命运特化将转录网络从桑椹胚样状态改变为指定为EPI的状态,并激活TEAD-YAP以触发与NANOG的正反馈回路,从而稳定EPI命运。在单个细胞中这些过程的协调发生可能支持在异步EPI命运特化条件下正确的EPI形成。