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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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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. |
format | Online Article Text |
id | pubmed-5981164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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