Inducible degradation of lncRNA Sros1 promotes IFN-γ-mediated activation of innate immune responses by stabilizing Stat1 mRNA

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作者
Henan Xu
Yan Jiang
Xiaoqing Xu
Xiaoping Su
Yang Liu
Yuanwu Ma
Yong Zhao
Zhongyang Shen
Bo Huang
Xuetao Cao
机构
[1] Chinese Academy of Medical Sciences,Department of Immunology & Center for Immunotherapy, Institute of Basic Medical Sciences, Peking Union Medical College
[2] Second Military Medical University,National Key Laboratory of Medical Immunology & Institute of Immunology
[3] Chinese Academy of Medical Sciences,Institute of Laboratory Animal Science
[4] Chinese Academy of Medical Sciences,Fuwai Central China Cardiovascular Hospital
[5] Tianjin First Center Hospital,College of Life Sciences
[6] Nankai University,undefined
来源
Nature Immunology | 2019年 / 20卷
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摘要
Interferon-γ (IFN-γ) is essential for the innate immune response to intracellular bacteria. Noncoding RNAs and RNA-binding proteins (RBPs) need to be further considered in studies of regulation of the IFN-γ-activated signaling pathway in macrophages. In the present study, we found that the microRNA miR-1 promoted IFN-γ-mediated clearance of Listeria monocytogenes in macrophages by indirectly stabilizing the Stat1 messenger RNA through the degradation of the cytoplasmic long noncoding RNA Sros1. Inducible degradation or genetic loss of Sros1 led to enhanced IFN-γ-dependent activation of the innate immune response. Mechanistically, Sros1 blocked the binding of Stat1 mRNA to the RBP CAPRIN1, which stabilized the Stat1 mRNA and, consequently, promoted IFN-γ–STAT1-mediated innate immunity. These observations shed light on the complex RNA–RNA regulatory networks involved in cytokine-initiated innate responses in host–pathogen interactions.
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页码:1621 / 1630
页数:9
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