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miR-21-3p Regulates Influenza A Virus Replication by Targeting Histone Deacetylase-8

Influenza A virus (IAV) is responsible for severe morbidity and mortality in animals and humans worldwide. miRNAs are a class of small noncoding single-stranded RNA molecules that can negatively regulate gene expression and play important roles in virus-host interaction. However, the roles of miRNAs...

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Autores principales: Xia, Binghui, Lu, Jiansheng, Wang, Rong, Yang, Zhixin, Zhou, Xiaowei, Huang, Peitang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5981164/
https://www.ncbi.nlm.nih.gov/pubmed/29888214
http://dx.doi.org/10.3389/fcimb.2018.00175
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author Xia, Binghui
Lu, Jiansheng
Wang, Rong
Yang, Zhixin
Zhou, Xiaowei
Huang, Peitang
author_facet Xia, Binghui
Lu, Jiansheng
Wang, Rong
Yang, Zhixin
Zhou, Xiaowei
Huang, Peitang
author_sort Xia, Binghui
collection PubMed
description Influenza A virus (IAV) is responsible for severe morbidity and mortality in animals and humans worldwide. miRNAs are a class of small noncoding single-stranded RNA molecules that can negatively regulate gene expression and play important roles in virus-host interaction. However, the roles of miRNAs in IAV infection are still not fully understood. Here, we profiled the cellular miRNAs of A549 cells infected with A/goose/Jilin/hb/2003 (H5N1) and a comparison A/Beijing/501/2009 (H1N1). miRNA microarray and quantitative PCR analysis showed that several miRNAs were differentially expressed in A549 cells during IAV infection. Subsequently, we demonstrated that IAV replication was essential for the regulation of these miRNAs, and bioinformatic analysis revealed that the targets of these miRNAs affected biological processes relevant to IAV replication. Specifically, miR-21-3p was found to be down-regulated in IAV-infected A549 cells and selected for further detailed analysis. Target prediction and functional study illustrated that miR-21-3p repressed the expression of HDAC8 by targeting its 3′UTR. Furthermore, we confirmed miR-21-3p could promote virus replication, which was similar to the result of knocking down HDAC8, indicating that miR-21-3p promoted IAV replication by suppressing HDAC8 expression. Altogether, our results suggest a potential host defense against IAV through down-regulation of miR-21-3p.
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spelling pubmed-59811642018-06-08 miR-21-3p Regulates Influenza A Virus Replication by Targeting Histone Deacetylase-8 Xia, Binghui Lu, Jiansheng Wang, Rong Yang, Zhixin Zhou, Xiaowei Huang, Peitang Front Cell Infect Microbiol Microbiology Influenza A virus (IAV) is responsible for severe morbidity and mortality in animals and humans worldwide. miRNAs are a class of small noncoding single-stranded RNA molecules that can negatively regulate gene expression and play important roles in virus-host interaction. However, the roles of miRNAs in IAV infection are still not fully understood. Here, we profiled the cellular miRNAs of A549 cells infected with A/goose/Jilin/hb/2003 (H5N1) and a comparison A/Beijing/501/2009 (H1N1). miRNA microarray and quantitative PCR analysis showed that several miRNAs were differentially expressed in A549 cells during IAV infection. Subsequently, we demonstrated that IAV replication was essential for the regulation of these miRNAs, and bioinformatic analysis revealed that the targets of these miRNAs affected biological processes relevant to IAV replication. Specifically, miR-21-3p was found to be down-regulated in IAV-infected A549 cells and selected for further detailed analysis. Target prediction and functional study illustrated that miR-21-3p repressed the expression of HDAC8 by targeting its 3′UTR. Furthermore, we confirmed miR-21-3p could promote virus replication, which was similar to the result of knocking down HDAC8, indicating that miR-21-3p promoted IAV replication by suppressing HDAC8 expression. Altogether, our results suggest a potential host defense against IAV through down-regulation of miR-21-3p. Frontiers Media S.A. 2018-05-25 /pmc/articles/PMC5981164/ /pubmed/29888214 http://dx.doi.org/10.3389/fcimb.2018.00175 Text en Copyright © 2018 Xia, Lu, Wang, Yang, Zhou and Huang. http://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 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
Xia, Binghui
Lu, Jiansheng
Wang, Rong
Yang, Zhixin
Zhou, Xiaowei
Huang, Peitang
miR-21-3p Regulates Influenza A Virus Replication by Targeting Histone Deacetylase-8
title miR-21-3p Regulates Influenza A Virus Replication by Targeting Histone Deacetylase-8
title_full miR-21-3p Regulates Influenza A Virus Replication by Targeting Histone Deacetylase-8
title_fullStr miR-21-3p Regulates Influenza A Virus Replication by Targeting Histone Deacetylase-8
title_full_unstemmed miR-21-3p Regulates Influenza A Virus Replication by Targeting Histone Deacetylase-8
title_short miR-21-3p Regulates Influenza A Virus Replication by Targeting Histone Deacetylase-8
title_sort mir-21-3p regulates influenza a virus replication by targeting histone deacetylase-8
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5981164/
https://www.ncbi.nlm.nih.gov/pubmed/29888214
http://dx.doi.org/10.3389/fcimb.2018.00175
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