全能的
重编程
胚胎干细胞
细胞生物学
下调和上调
诱导多能干细胞
干细胞
DNMT1型
生物
细胞分化
细胞
基因表达
遗传学
DNA甲基化
基因
作者
Xudong Fu,Xiaoji Wu,Mohamed Nadhir Djekidel,Yi Zhang
标识
DOI:10.1038/s41556-019-0343-0
摘要
Totipotency refers to the ability of a cell to generate all of the cell types of an organism. Unlike pluripotency, the establishment of totipotency is poorly understood. In mouse embryonic stem cells, Dux drives a small percentage of cells into a totipotent state by expressing 2-cell-embryo-specific transcripts. To understand how this transition takes place, we performed single-cell RNA-seq, which revealed a two-step transcriptional reprogramming process characterized by downregulation of pluripotent genes in the first step and upregulation of the 2-cell-embryo-specific elements in the second step. To identify factors controlling the transition, we performed a CRISPR–Cas9-mediated screen, which revealed Myc and Dnmt1 as two factors preventing the transition. Mechanistic studies demonstrate that Myc prevents downregulation of pluripotent genes in the first step, while Dnmt1 impedes 2-cell-embryo-specific gene activation in the second step. Collectively, the findings of our study reveal insights into the establishment and regulation of the totipotent state in mouse embryonic stem cells. Fu et al. report the transition of ESCs into a 2-cell-embyro-like state induced by Dux involves two steps and can be prevented by Myc and Dnmt1, which inhibit the downregulation of pluripotency genes and the activation of 2C+-upregulated elements.
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