ILF3 represses repeat-derived microRNAs targeting RIG-I mediated type I interferon response

被引:3
|
作者
Chen, Geng [1 ]
Yang, Yang [1 ]
Wu, Qi-Jia [2 ]
Cao, Liu [1 ]
Ruan, Wen [1 ]
Shao, Changwei [1 ,3 ]
Jiang, Li [1 ]
Tang, Peng [1 ]
Ma, Suping [1 ]
Jiang, Ao [1 ]
Wang, Zhen [1 ]
Wu, Kai [1 ]
Zhang, Qiangfeng Cliff [4 ]
Fu, Xiang-Dong [3 ]
Zhou, Yu [1 ]
机构
[1] Wuhan Univ, Coll Life Sci, State Key Lab Virol, Hubei Key Lab Cell Homeostasis, Wuhan, Peoples R China
[2] Seqhealth Technol Co Ltd, Wuhan, Peoples R China
[3] Univ Calif, Inst Genom Med, Dept Cellular & Mol Med, San Diego, CA USA
[4] Tsinghua Univ, Beijing Adv Innovat Ctr Struct Biol, Ctr Synthet & Syst Biol, Tsinghua Peking Ctr Life Sci,Sch Life Sci,MOE, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
ILF3; miRNA biogenesis; repeat-derived miRNAs; microprocessor; antiviral response; MIRNA BIOGENESIS; MOLECULAR-BASIS; NFAR PROTEINS; RECOGNITION; BINDING; MICROPROCESSOR; SEQUENCE; MODULATION; EXPRESSION; REGULATOR;
D O I
10.1016/j.jmb.2022.167469
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) play important roles in regulated gene expression and miRNA biogenesis is also subject to regulation, together constituting critical regulatory circuitries in numerous physiological and pathological processes. As a dsRNA binding protein, interleukin enhancer binding factor 3 (ILF3) has been implicated as a negative regulator in miRNA biogenesis, but the mechanism and specificity have remained undefined. Here, combining small-RNA-seq and CLIP-seq, we showed that ILF3 directly represses many miRNAs or perhaps other types of small RNAs annotated in both miRBase and MirGeneDB. We demonstrated that ILF3 preferentially binds to A/U-enriched motifs, which tend to lengthen and/ or stabilize the stem-loop in pri-miRNAs, thereby effectively competing with the Microprocessor to block miRNA biogenesis. Focusing on the biological function of ILF3-suppressed miR-582-3p, we discovered that this LINE-derived miRNA targets a critical interferon-inducible gene RIG-I for repression, thus establishing a novel ILF3/miR-582/RIG-I axis in the antiviral response. (c) 2022 Elsevier Ltd. All rights reserved.
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页数:18
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