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The regulation of antiviral innate immunity through non-m(6)A RNA modifications
The post-transcriptional RNA modifications impact the dynamic regulation of gene expression in diverse biological and physiological processes. Host RNA modifications play an indispensable role in regulating innate immune responses against virus infection in mammals. Meanwhile, the viral RNAs can be...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10616867/ https://www.ncbi.nlm.nih.gov/pubmed/37915585 http://dx.doi.org/10.3389/fimmu.2023.1286820 |
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author | Shen, Shenghai Zhang, Li-Sheng |
author_facet | Shen, Shenghai Zhang, Li-Sheng |
author_sort | Shen, Shenghai |
collection | PubMed |
description | The post-transcriptional RNA modifications impact the dynamic regulation of gene expression in diverse biological and physiological processes. Host RNA modifications play an indispensable role in regulating innate immune responses against virus infection in mammals. Meanwhile, the viral RNAs can be deposited with RNA modifications to interfere with the host immune responses. The N(6)-methyladenosine (m(6)A) has boosted the recent emergence of RNA epigenetics, due to its high abundance and a transcriptome-wide widespread distribution in mammalian cells, proven to impact antiviral innate immunity. However, the other types of RNA modifications are also involved in regulating antiviral responses, and the functional roles of these non-m(6)A RNA modifications have not been comprehensively summarized. In this Review, we conclude the regulatory roles of 2’-O-methylation (Nm), 5-methylcytidine (m(5)C), adenosine-inosine editing (A-to-I editing), pseudouridine (Ψ), N(1)-methyladenosine (m(1)A), N(7)-methylguanosine (m(7)G), N(6),2’-O-dimethyladenosine (m(6)Am), and N(4)-acetylcytidine (ac(4)C) in antiviral innate immunity. We provide a systematic introduction to the biogenesis and functions of these non-m(6)A RNA modifications in viral RNA, host RNA, and during virus-host interactions, emphasizing the biological functions of RNA modification regulators in antiviral responses. Furthermore, we discussed the recent research progress in the development of antiviral drugs through non-m(6)A RNA modifications. Collectively, this Review conveys knowledge and inspiration to researchers in multiple disciplines, highlighting the challenges and future directions in RNA epitranscriptome, immunology, and virology. |
format | Online Article Text |
id | pubmed-10616867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106168672023-11-01 The regulation of antiviral innate immunity through non-m(6)A RNA modifications Shen, Shenghai Zhang, Li-Sheng Front Immunol Immunology The post-transcriptional RNA modifications impact the dynamic regulation of gene expression in diverse biological and physiological processes. Host RNA modifications play an indispensable role in regulating innate immune responses against virus infection in mammals. Meanwhile, the viral RNAs can be deposited with RNA modifications to interfere with the host immune responses. The N(6)-methyladenosine (m(6)A) has boosted the recent emergence of RNA epigenetics, due to its high abundance and a transcriptome-wide widespread distribution in mammalian cells, proven to impact antiviral innate immunity. However, the other types of RNA modifications are also involved in regulating antiviral responses, and the functional roles of these non-m(6)A RNA modifications have not been comprehensively summarized. In this Review, we conclude the regulatory roles of 2’-O-methylation (Nm), 5-methylcytidine (m(5)C), adenosine-inosine editing (A-to-I editing), pseudouridine (Ψ), N(1)-methyladenosine (m(1)A), N(7)-methylguanosine (m(7)G), N(6),2’-O-dimethyladenosine (m(6)Am), and N(4)-acetylcytidine (ac(4)C) in antiviral innate immunity. We provide a systematic introduction to the biogenesis and functions of these non-m(6)A RNA modifications in viral RNA, host RNA, and during virus-host interactions, emphasizing the biological functions of RNA modification regulators in antiviral responses. Furthermore, we discussed the recent research progress in the development of antiviral drugs through non-m(6)A RNA modifications. Collectively, this Review conveys knowledge and inspiration to researchers in multiple disciplines, highlighting the challenges and future directions in RNA epitranscriptome, immunology, and virology. Frontiers Media S.A. 2023-10-17 /pmc/articles/PMC10616867/ /pubmed/37915585 http://dx.doi.org/10.3389/fimmu.2023.1286820 Text en Copyright © 2023 Shen and Zhang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Shen, Shenghai Zhang, Li-Sheng The regulation of antiviral innate immunity through non-m(6)A RNA modifications |
title | The regulation of antiviral innate immunity through non-m(6)A RNA modifications |
title_full | The regulation of antiviral innate immunity through non-m(6)A RNA modifications |
title_fullStr | The regulation of antiviral innate immunity through non-m(6)A RNA modifications |
title_full_unstemmed | The regulation of antiviral innate immunity through non-m(6)A RNA modifications |
title_short | The regulation of antiviral innate immunity through non-m(6)A RNA modifications |
title_sort | regulation of antiviral innate immunity through non-m(6)a rna modifications |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10616867/ https://www.ncbi.nlm.nih.gov/pubmed/37915585 http://dx.doi.org/10.3389/fimmu.2023.1286820 |
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