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N(6)-methyladenosine modification of the Aedes aegypti transcriptome and its alteration upon dengue virus infection in Aag2 cell line

The N(6)-methyladenosine (m(6)A) modification of RNA has been reported to affect viral infections. Studies have confirmed the role of m(6)A in replication of several vector-borne flaviviruses, including dengue virus (DENV), in mammalian cells. Here, we explored the role of m(6)A in DENV replication...

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Autores principales: Dai, Zhenkai, Etebari, Kayvan, Asgari, Sassan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9209429/
https://www.ncbi.nlm.nih.gov/pubmed/35725909
http://dx.doi.org/10.1038/s42003-022-03566-8
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author Dai, Zhenkai
Etebari, Kayvan
Asgari, Sassan
author_facet Dai, Zhenkai
Etebari, Kayvan
Asgari, Sassan
author_sort Dai, Zhenkai
collection PubMed
description The N(6)-methyladenosine (m(6)A) modification of RNA has been reported to affect viral infections. Studies have confirmed the role of m(6)A in replication of several vector-borne flaviviruses, including dengue virus (DENV), in mammalian cells. Here, we explored the role of m(6)A in DENV replication in the mosquito Aedes aegypti Aag2 cell line. We first determined the presence of m(6)A on the RNAs from mosquito cells and using methylated RNA immunoprecipitation and sequencing (MeRIP-Seq) identified m(6)A modification of the mosquito transcriptome and those that changed upon DENV infection. Depletion of m(6)A methyltransferases and the m(6)A binding protein YTHDF3 RNAs decreased the replication of DENV. In particular, we found that the Ae. aegypti ubiquitin carrier protein 9 (Ubc9) is m(6)A modified and its expression increases after DENV infection. Silencing of the gene and ectopic expression of Ubc9 led to reduced and increased DENV replication, respectively. The abundance of Ubc9 mRNA and its stability were reduced with the inhibition of m(6)A modification, implying that m(6)A modification of Ubc9 might enhance expression of the gene. We also show that the genome of DENV is m(6)A modified at five sites in mosquito cells. Altogether, this work reveals the involvement of m(6)A modification in Ae. aegypti-DENV interaction.
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spelling pubmed-92094292022-06-22 N(6)-methyladenosine modification of the Aedes aegypti transcriptome and its alteration upon dengue virus infection in Aag2 cell line Dai, Zhenkai Etebari, Kayvan Asgari, Sassan Commun Biol Article The N(6)-methyladenosine (m(6)A) modification of RNA has been reported to affect viral infections. Studies have confirmed the role of m(6)A in replication of several vector-borne flaviviruses, including dengue virus (DENV), in mammalian cells. Here, we explored the role of m(6)A in DENV replication in the mosquito Aedes aegypti Aag2 cell line. We first determined the presence of m(6)A on the RNAs from mosquito cells and using methylated RNA immunoprecipitation and sequencing (MeRIP-Seq) identified m(6)A modification of the mosquito transcriptome and those that changed upon DENV infection. Depletion of m(6)A methyltransferases and the m(6)A binding protein YTHDF3 RNAs decreased the replication of DENV. In particular, we found that the Ae. aegypti ubiquitin carrier protein 9 (Ubc9) is m(6)A modified and its expression increases after DENV infection. Silencing of the gene and ectopic expression of Ubc9 led to reduced and increased DENV replication, respectively. The abundance of Ubc9 mRNA and its stability were reduced with the inhibition of m(6)A modification, implying that m(6)A modification of Ubc9 might enhance expression of the gene. We also show that the genome of DENV is m(6)A modified at five sites in mosquito cells. Altogether, this work reveals the involvement of m(6)A modification in Ae. aegypti-DENV interaction. Nature Publishing Group UK 2022-06-20 /pmc/articles/PMC9209429/ /pubmed/35725909 http://dx.doi.org/10.1038/s42003-022-03566-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Dai, Zhenkai
Etebari, Kayvan
Asgari, Sassan
N(6)-methyladenosine modification of the Aedes aegypti transcriptome and its alteration upon dengue virus infection in Aag2 cell line
title N(6)-methyladenosine modification of the Aedes aegypti transcriptome and its alteration upon dengue virus infection in Aag2 cell line
title_full N(6)-methyladenosine modification of the Aedes aegypti transcriptome and its alteration upon dengue virus infection in Aag2 cell line
title_fullStr N(6)-methyladenosine modification of the Aedes aegypti transcriptome and its alteration upon dengue virus infection in Aag2 cell line
title_full_unstemmed N(6)-methyladenosine modification of the Aedes aegypti transcriptome and its alteration upon dengue virus infection in Aag2 cell line
title_short N(6)-methyladenosine modification of the Aedes aegypti transcriptome and its alteration upon dengue virus infection in Aag2 cell line
title_sort n(6)-methyladenosine modification of the aedes aegypti transcriptome and its alteration upon dengue virus infection in aag2 cell line
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9209429/
https://www.ncbi.nlm.nih.gov/pubmed/35725909
http://dx.doi.org/10.1038/s42003-022-03566-8
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