Chromatin remodeler Znhit1 preserves hematopoietic stem cell quiescence by determining the accessibility of distal enhancers

作者：Shenfei Sun, Ning Jiang, Yamei Jiang, Qiuping He, Hua He, Xin Wang, Yang Li, Li R, Feng Liu, Xinhua Lin, Bing Zhao · 发表于：Leukemia · 年份：2020 · DOI：10.1038/s41375-020-0988-5 · 被引用次数：29 · 研究领域：Immune Cell Function and Interaction、Hematopoietic Stem Cell Transplantation、Acute Myeloid Leukemia Research

Hematopoietic stem cell (HSC) utilizes its quiescence feature to combat exhaustion for lifetime blood cell supply. To date, how certain chromatin architecture and subsequent transcription profile permit HSC quiescence remains unclear. Here, we show an essential role of chromatin remodeler zinc finger HIT-type containing 1 (Znhit1) in maintaining HSC quiescence. We find that loss of Znhit1 leads to exhaustion of stem cell pool and impairment of hematopoietic function. Mechanically, Znhit1 determines the chromatin accessibility at distal enhancers of HSC quiescence genes, including Pten, Fstl1, and Klf4, for sustained transcription and consequent PI3K-Akt signaling inhibition. Moreover, Znhit1-Pten-PI3K-Akt axis also participates in controlling myeloid expansion and B-lymphoid specification. Our findings therefore identify a dominant role of Znhit1-mediated chromatin remodeling in preserving HSC function for hematopoietic homeostasis.