Yang Shangda, Sun Guohuan, Wu Peng, Chen Cong, Kuang Yijin, Liu Ling, Zheng Zhaofeng, He Yicheng, Gu Quan, Lu Ting, Zhu Caiying, Wang Fengjiao, Gou Fanglin, Yang Zining, Zhao Xiangnan, Yuan Shiru, Yang Liu, Lu Shihong, Li Yapu, Lv Xue, Dong Fang, Ma Yanni, Yu Jia, Ng Lai Guan, Shi Lihong, Liu Jing, Shi Lei, Cheng Tao, Cheng Hui
State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
Center for Stem Cell Medicine, Department of Stem Cell and Regenerative Medicine, Chinese Academy of Medical Sciences, Tianjin, China.
J Exp Med. 2022 Apr 4;219(4). doi: 10.1084/jem.20211688. Epub 2022 Mar 22.
Hematopoietic differentiation is controlled by both genetic and epigenetic regulators. Long noncoding RNAs (lncRNAs) have been demonstrated to be important for normal hematopoiesis, but their function in erythropoiesis needs to be further explored. We profiled the transcriptomes of 16 murine hematopoietic cell populations by deep RNA sequencing and identified a novel lncRNA, Gm15915, that was highly expressed in erythroid-related progenitors and erythrocytes. For this reason, we named it lncEry. We also identified a novel lncEry isoform, which was the principal transcript that has not been reported before. lncEry depletion impaired erythropoiesis, indicating the important role of the lncRNA in regulating erythroid differentiation and maturation. Mechanistically, we found that lncEry interacted with WD repeat-containing protein 82 (WDR82) to promote the transcription of Klf1 and globin genes and thus control the early and late stages of erythropoiesis, respectively. These findings identified lncEry as an important player in the transcriptional regulation of erythropoiesis.
造血分化受遗传和表观遗传调节因子的共同控制。长链非编码RNA(lncRNAs)已被证明对正常造血至关重要,但其在红细胞生成中的功能仍有待进一步探索。我们通过深度RNA测序分析了16个小鼠造血细胞群体的转录组,并鉴定出一种新型lncRNA,即Gm15915,它在红系相关祖细胞和红细胞中高表达。因此,我们将其命名为lncEry。我们还鉴定出一种新型lncEry异构体,它是之前未报道过的主要转录本。lncEry的缺失损害了红细胞生成,表明该lncRNA在调节红系分化和成熟中发挥重要作用。机制上,我们发现lncEry与含WD重复序列蛋白82(WDR82)相互作用,分别促进Klf1和珠蛋白基因的转录,从而控制红细胞生成的早期和晚期阶段。这些发现确定lncEry是红细胞生成转录调控中的一个重要因子。