同源盒蛋白纳米
外胚层
SOX2
生物
细胞生物学
纳米同源盒蛋白
转录因子
细胞命运测定
胚胎
胚胎干细胞
正面反馈
遗传学
原肠化
胚胎发生
基因
诱导多能干细胞
工程类
电气工程
作者
Naoki Hirono,Masakazu Hashimoto,Hiromi Shimojo,Hiroshi Sasaki
出处
期刊:Development
[The Company of Biologists]
日期:2024-12-04
摘要
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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