A Feedback Loop Consisting of MicroRNA 23a/27a and the β-Like Globin Suppressors KLF3 and SP1 Regulates Globin Gene Expression

Author:

Ma Yanni1,Wang Bin1,Jiang Fengbing1,Wang Dongsheng2,Liu Huiwen1,Yan Yunmeng1,Dong He1,Wang Fang1,Gong Bei1,Zhu Yong1,Dong Lei1,Yin Haixin1,Zhang Zhongzu1,Zhao Hualu1,Wu Zhikui3,Zhang Junwu1,Zhou Jingguo2,Yu Jia1

Affiliation:

1. Department of Biochemistry, State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, People's Republic of China

2. Department of Laboratory Medicine, Affiliated Hospital of North Sichuan Medical College, Nanchong, People's Republic of China

3. Molecular Biology Laboratory of Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, People's Republic of China

Abstract

ABSTRACT The developmental stage-specific expression of the human β-like globin genes has been studied for decades, and many transcriptional factors as well as other important cis elements have been identified. However, little is known about the microRNAs that potentially regulate β-like globin gene expression directly or indirectly during erythropoiesis. In this study, we show that microRNA 23a (miR-23a) and miR-27a promote β-like globin gene expression in K562 cells and primary erythroid cells through targeting of the transcription factors KLF3 and SP1. Intriguingly, miR-23a and miR-27a further enhance the transcription of β-like globin genes through repression of KLF3 and SP1 binding to the β-like globin gene locus during erythroid differentiation. Moreover, KLF3 can bind to the promoter of the miR-23a∼27a∼24-2 cluster and suppress this microRNA cluster expression. Hence, a positive feedback loop comprised of KLF3 and miR-23a promotes the expression of β-like globin genes and the miR-23a∼27a∼24-2 cluster during erythropoiesis.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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