1. Academic Validation
  2. Distinct pathways utilized by METTL3 to regulate antiviral innate immune response

Distinct pathways utilized by METTL3 to regulate antiviral innate immune response

  • iScience. 2024 Sep 30;27(11):111071. doi: 10.1016/j.isci.2024.111071.
Haojie Hao 1 2 Fang Zhang 2 Zhen Chen 1 Zhongyuan Tan 1 Hongyan Zhang 3 Xumei Feng 2 Xueyan Zhang 1 Tao Deng 1 Guanli Zhan 4 Ting Luo 1 Kui Zhang 1 Shuang Ding 1 Haibin Liu 1 Zhenhua Zheng 1 Yanyi Wang 1 Fang Huang 2 Wuxiang Guan 1 2
Affiliations

Affiliations

  • 1 Center for Emerging Infectious Diseases, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, Hubei 430071, China.
  • 2 Hubei JiangXia Laboratory, Wuhan, Hubei 430200, China.
  • 3 Department of Dermatology, Hangzhou Third People's Hospital, Hangzhou, Zhejiang 310009, China.
  • 4 Department of PathogenBiology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430030, China.
Abstract

Methyltransferase-like 3 (METTL3), the core methyltransferase for N 6-methyladenosine (m6A), plays a crucial role in innate immunity by introducing m6A modifications on viral or host RNAs. Despite its well-established catalytic function in m6A deposition, the broader role of METTL3 in immune regulation remains unclear. Here, we uncovered that EV71 Infection enhanced METTL3 expression in interferon (IFN)-deficient Vero and IFN-proficient rhabdomyosarcoma (RD) cells by modulating transcription and post-translational modification, respectively. METTL3 was shown to regulate Antiviral immune responses in both m6A-dependent and -independent manners. METTL3's catalytic motif impaired viral RNA recognition by retinoic-acid-inducible gene I (RIG-I) via m6A modification, whereas its non-catalytic motif recruited and stabilized DEAD-box helicase 3X (DDX3X) by preventing DDX3X ubiquitination, which all mediate immune inhibition. This study reveals an m6A-independent pathway through which METTL3 regulates immune responses, highlighting its potential as a target for Antiviral therapy.

Keywords

Immunology; Molecular biology; Virology.

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