染色质
胚胎干细胞
组蛋白
细胞生物学
生物
多组蛋白
基因
核糖核酸
细胞
遗传学
基因表达
抑制因子
作者
Jingyuan Zhang,Tianyu Wang,Ruona Shi,Yuan Zhao,Yanqi Zhang,Cong Zhang,Xing Qi,Tiancheng Zhou,Yongli Shan,Hongjie Yao,Xiaofei Zhang,Guangjin Pan
摘要
Abstract Polycomb repressive complexes (PRCs) play critical roles in cell fate decisions during normal development as well as disease progression through mediating histone modifications such as H3K27me3 and H2AK119ub. How exactly PRCs recruited to chromatin remains to be fully illuminated. Here, we report that YTHDF1, the N6‐methyladenine (m 6 A) RNA reader that was previously known to be mainly cytoplasmic, associates with RNF2, a PRC1 protein that mediates H2AK119ub in human embryonic stem cells (hESCs). A portion of YTHDF1 localizes in the nuclei and associates with RNF2/H2AK119ub on a subset of gene loci related to neural development functions. Knock‐down YTHDF1 attenuates H2AK119ub modification on these genes and promotes neural differentiation in hESCs. Our findings provide a noncanonical mechanism that YTHDF1 participates in PRC1 functions in hESCs.
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