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Histone acetyl transferase TIP60 inhibits the replication of influenza a virus by activation the TBK1-IRF3 pathway
Influenza A virus (IAV) is an important pathogen that poses a severe threat to the health of humans. Nucleoprotein (NP) of IAV plays crucial roles in the viral life cycle by interacting with various cellular factors. Histone Acetyl Transferase TIP60 is a key target of several viral proteins during i...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6225679/ https://www.ncbi.nlm.nih.gov/pubmed/30409205 http://dx.doi.org/10.1186/s12985-018-1079-3 |
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author | Ma, Guoyao Chen, Lin Luo, Jing Wang, Bo Wang, Chengmin Li, Meng Huang, Chengmei Du, Juan Ma, Jiajun Chang, Yungfu He, Hongxuan |
author_facet | Ma, Guoyao Chen, Lin Luo, Jing Wang, Bo Wang, Chengmin Li, Meng Huang, Chengmei Du, Juan Ma, Jiajun Chang, Yungfu He, Hongxuan |
author_sort | Ma, Guoyao |
collection | PubMed |
description | Influenza A virus (IAV) is an important pathogen that poses a severe threat to the health of humans. Nucleoprotein (NP) of IAV plays crucial roles in the viral life cycle by interacting with various cellular factors. Histone Acetyl Transferase TIP60 is a key target of several viral proteins during infection, including HIV-1 Tat, HPV E6, HTLV-1 p30(II) and HCMV UL27 proteins. However, Whether the interaction between the IAV NP and TIP60, and the role of TIP60 in IAV life cycle are largely unknown. Here, we showed that IAV infection up-regulated TIP60 protein and RNA expression. Overexpression of TIP60 inhibited viral protein and RNA expression and reduced the progeny viral titer. Further study revealed that TIP60 inhibited viral replication through activation of TBK1-IRF3 signaling pathway. Furthermore, we demonstrated that the NP protein of IAV interacted with TIP60. Together, these results indicate that TIP60 play a repressor in IAV infection, and it may be a possible target for antiviral drugs. |
format | Online Article Text |
id | pubmed-6225679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62256792018-11-19 Histone acetyl transferase TIP60 inhibits the replication of influenza a virus by activation the TBK1-IRF3 pathway Ma, Guoyao Chen, Lin Luo, Jing Wang, Bo Wang, Chengmin Li, Meng Huang, Chengmei Du, Juan Ma, Jiajun Chang, Yungfu He, Hongxuan Virol J Research Influenza A virus (IAV) is an important pathogen that poses a severe threat to the health of humans. Nucleoprotein (NP) of IAV plays crucial roles in the viral life cycle by interacting with various cellular factors. Histone Acetyl Transferase TIP60 is a key target of several viral proteins during infection, including HIV-1 Tat, HPV E6, HTLV-1 p30(II) and HCMV UL27 proteins. However, Whether the interaction between the IAV NP and TIP60, and the role of TIP60 in IAV life cycle are largely unknown. Here, we showed that IAV infection up-regulated TIP60 protein and RNA expression. Overexpression of TIP60 inhibited viral protein and RNA expression and reduced the progeny viral titer. Further study revealed that TIP60 inhibited viral replication through activation of TBK1-IRF3 signaling pathway. Furthermore, we demonstrated that the NP protein of IAV interacted with TIP60. Together, these results indicate that TIP60 play a repressor in IAV infection, and it may be a possible target for antiviral drugs. BioMed Central 2018-11-08 /pmc/articles/PMC6225679/ /pubmed/30409205 http://dx.doi.org/10.1186/s12985-018-1079-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ma, Guoyao Chen, Lin Luo, Jing Wang, Bo Wang, Chengmin Li, Meng Huang, Chengmei Du, Juan Ma, Jiajun Chang, Yungfu He, Hongxuan Histone acetyl transferase TIP60 inhibits the replication of influenza a virus by activation the TBK1-IRF3 pathway |
title | Histone acetyl transferase TIP60 inhibits the replication of influenza a virus by activation the TBK1-IRF3 pathway |
title_full | Histone acetyl transferase TIP60 inhibits the replication of influenza a virus by activation the TBK1-IRF3 pathway |
title_fullStr | Histone acetyl transferase TIP60 inhibits the replication of influenza a virus by activation the TBK1-IRF3 pathway |
title_full_unstemmed | Histone acetyl transferase TIP60 inhibits the replication of influenza a virus by activation the TBK1-IRF3 pathway |
title_short | Histone acetyl transferase TIP60 inhibits the replication of influenza a virus by activation the TBK1-IRF3 pathway |
title_sort | histone acetyl transferase tip60 inhibits the replication of influenza a virus by activation the tbk1-irf3 pathway |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6225679/ https://www.ncbi.nlm.nih.gov/pubmed/30409205 http://dx.doi.org/10.1186/s12985-018-1079-3 |
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