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EBV Exploits RNA m(6)A Modification to Promote Cell Survival and Progeny Virus Production During Lytic Cycle
N6-methyladenosine (m(6)A) mediates various biological processes by affecting RNA stability, splicing, and translational efficiency. The roles of m(6)A modification in Epstein-Barr virus (EBV) infection in the lytic phase are unclear. Here, knockout of the m(6)A methyltransferase, N6-methyladenosine...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240777/ https://www.ncbi.nlm.nih.gov/pubmed/35783391 http://dx.doi.org/10.3389/fmicb.2022.870816 |
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author | Yanagi, Yusuke Watanabe, Takahiro Hara, Yuya Sato, Yoshitaka Kimura, Hiroshi Murata, Takayuki |
author_facet | Yanagi, Yusuke Watanabe, Takahiro Hara, Yuya Sato, Yoshitaka Kimura, Hiroshi Murata, Takayuki |
author_sort | Yanagi, Yusuke |
collection | PubMed |
description | N6-methyladenosine (m(6)A) mediates various biological processes by affecting RNA stability, splicing, and translational efficiency. The roles of m(6)A modification in Epstein-Barr virus (EBV) infection in the lytic phase are unclear. Here, knockout of the m(6)A methyltransferase, N6-methyladenosine methyltransferase-like 3 (METTL3), or inhibition of methylation by DAA or UZH1a decreased the expression of viral lytic proteins and reduced progeny virion production. Interestingly, cell growth and viability were decreased by induction of the lytic cycle in METTL3-knockout or inhibitor-treated cells. Apoptosis was induced in those conditions possibly because of a decreased level of the anti-apoptotic viral protein, BHRF1. Therefore, m(6)A shows potential as a target of lytic induction therapy for EBV-associated cancers, including Burkitt lymphoma. |
format | Online Article Text |
id | pubmed-9240777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92407772022-06-30 EBV Exploits RNA m(6)A Modification to Promote Cell Survival and Progeny Virus Production During Lytic Cycle Yanagi, Yusuke Watanabe, Takahiro Hara, Yuya Sato, Yoshitaka Kimura, Hiroshi Murata, Takayuki Front Microbiol Microbiology N6-methyladenosine (m(6)A) mediates various biological processes by affecting RNA stability, splicing, and translational efficiency. The roles of m(6)A modification in Epstein-Barr virus (EBV) infection in the lytic phase are unclear. Here, knockout of the m(6)A methyltransferase, N6-methyladenosine methyltransferase-like 3 (METTL3), or inhibition of methylation by DAA or UZH1a decreased the expression of viral lytic proteins and reduced progeny virion production. Interestingly, cell growth and viability were decreased by induction of the lytic cycle in METTL3-knockout or inhibitor-treated cells. Apoptosis was induced in those conditions possibly because of a decreased level of the anti-apoptotic viral protein, BHRF1. Therefore, m(6)A shows potential as a target of lytic induction therapy for EBV-associated cancers, including Burkitt lymphoma. Frontiers Media S.A. 2022-06-15 /pmc/articles/PMC9240777/ /pubmed/35783391 http://dx.doi.org/10.3389/fmicb.2022.870816 Text en Copyright © 2022 Yanagi, Watanabe, Hara, Sato, Kimura and Murata. 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 | Microbiology Yanagi, Yusuke Watanabe, Takahiro Hara, Yuya Sato, Yoshitaka Kimura, Hiroshi Murata, Takayuki EBV Exploits RNA m(6)A Modification to Promote Cell Survival and Progeny Virus Production During Lytic Cycle |
title | EBV Exploits RNA m(6)A Modification to Promote Cell Survival and Progeny Virus Production During Lytic Cycle |
title_full | EBV Exploits RNA m(6)A Modification to Promote Cell Survival and Progeny Virus Production During Lytic Cycle |
title_fullStr | EBV Exploits RNA m(6)A Modification to Promote Cell Survival and Progeny Virus Production During Lytic Cycle |
title_full_unstemmed | EBV Exploits RNA m(6)A Modification to Promote Cell Survival and Progeny Virus Production During Lytic Cycle |
title_short | EBV Exploits RNA m(6)A Modification to Promote Cell Survival and Progeny Virus Production During Lytic Cycle |
title_sort | ebv exploits rna m(6)a modification to promote cell survival and progeny virus production during lytic cycle |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240777/ https://www.ncbi.nlm.nih.gov/pubmed/35783391 http://dx.doi.org/10.3389/fmicb.2022.870816 |
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