RNA编辑
生物
核糖核酸
造血
干细胞
RNA结合蛋白
细胞生物学
染色质
造血干细胞
遗传学
基因
作者
Fengjiao Wang,Jianyong He,Siqi Liu,Ai Gao,Yang Liu,Guoxiang Sun,Wanqiu Ding,Chuan-Yun Li,Fanglin Gou,Manman He,Fang Wang,Xiaoshuang Wang,Xiangnan Zhao,Ping Zhu,Sha Hao,Yupo Ma,Hui Cheng,Jia Yu,Tao Cheng
出处
期刊:Blood
[American Society of Hematology]
日期:2021-11-18
卷期号:138 (20): 1939-1952
被引量:25
标识
DOI:10.1182/blood.2021011314
摘要
Adenosine-to-inosine RNA editing and the catalyzing enzyme adenosine deaminase are both essential for hematopoietic development and differentiation. However, the RNA editome during hematopoiesis and the underlying mechanisms are poorly defined. Here, we sorted 12 murine adult hematopoietic cell populations at different stages and identified 30 796 editing sites through RNA sequencing. The dynamic landscape of the RNA editome comprises stage- and group-specific and stable editing patterns, but undergoes significant changes during lineage commitment. Notably, we found that antizyme inhibitor 1 (Azin1) was highly edited in hematopoietic stem and progenitor cells (HSPCs). Azin1 editing results in an amino acid change to induce Azin1 protein (AZI) translocation to the nucleus, enhanced AZI binding affinity for DEAD box polypeptide 1 to alter the chromatin distribution of the latter, and altered expression of multiple hematopoietic regulators that ultimately promote HSPC differentiation. Our findings have delineated an essential role for Azin1 RNA editing in hematopoietic cells, and our data set is a valuable resource for studying RNA editing on a more general basis.
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