Noncoding RNAcircBtnl1 suppresses self‐renewal of intestinal stem cells via disruption of Atf4 mRNA stability

Author:

Guo Hui1ORCID,Zhang Jiahang1,Jiang Zhimin1ORCID,Zhu Xiaoxiao2,Yang Jing3,Mu Rui3,Du Ying1,Tian Yong24ORCID,Zhu Pingping5ORCID,Fan Zusen14ORCID

Affiliation:

1. Key Laboratory of Infection and Immunity of CAS, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics Chinese Academy of Sciences Beijing China

2. Key Laboratory of RNA Biology, Institute of Biophysics Chinese Academy of Sciences Beijing China

3. Department of Physiology Hebei Medical University Shijiazhuang China

4. University of Chinese Academy of Sciences Beijing China

5. School of Life Sciences Zhengzhou University Zhengzhou China

Abstract

AbstractIntestinal stem cells (ISCs) at the crypt base are responsible for the regeneration of the intestinal epithelium. However, how ISC self‐renewal is regulated still remains unclear. Here we identified a circular RNA, circBtnl1, that is highly expressed in ISCs. Loss of circBtnl1 in mice enhanced ISC self‐renewal capacity and epithelial regeneration, without changes in mRNA and protein levels of its parental gene Btnl1. Mechanistically, circBtnl1 and Atf4 mRNA competitively bound the ATP‐dependent RNA helicase Ddx3y to impair the stability of Atf4 mRNA in wild‐type ISCs. Furthermore, ATF4 activated Sox9 transcription by binding to its promoter via a unique motif, to enhance the self‐renewal capacity and epithelial regeneration of ISCs. In contrast, circBtnl1 knockout promoted Atf4 mRNA stability and enhanced ATF4 expression, which caused Sox9 transcription to potentiate ISC stemness. These data indicate that circBtnl1‐mediated Atf4 mRNA decay suppresses Sox9 transcription that negatively modulates self‐renewal maintenance of ISCs.

Funder

National Natural Science Foundation of China

Publisher

Springer Science and Business Media LLC

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

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