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MicroRNA expression profiles from HEK293 cells expressing H5N1 avian influenza virus non-structural protein 1
H5N1 avian influenza poses a serious threat to the poultry industry and human health. Non-structural protein 1 (NS1) plays an important role in the replication and pathogenesis of avian influenza virus (AIV). However, the function of the NS1 gene is still unclear. In this study, illumina genome anal...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830863/ https://www.ncbi.nlm.nih.gov/pubmed/30782044 http://dx.doi.org/10.1177/1753425919826342 |
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author | Jiao, Hanwei Zheng, Zonglin Shuai, Xuehong Wu, Li Chen, Jixuan Luo, Yichen Zhao, Yu Wang, Hongjun Huang, Qingzhou |
author_facet | Jiao, Hanwei Zheng, Zonglin Shuai, Xuehong Wu, Li Chen, Jixuan Luo, Yichen Zhao, Yu Wang, Hongjun Huang, Qingzhou |
author_sort | Jiao, Hanwei |
collection | PubMed |
description | H5N1 avian influenza poses a serious threat to the poultry industry and human health. Non-structural protein 1 (NS1) plays an important role in the replication and pathogenesis of avian influenza virus (AIV). However, the function of the NS1 gene is still unclear. In this study, illumina genome analyzer iix screening was used to identify the differentially expressed microRNAs (miRNAs) in HEK293 cells expressing H5N1 AIV NS1. There were 13 differentially expressed miRNAs (hsa-miR-17-5p, hsa-miR-221-3p, hsa-miR-22-3p, hsa-miR-31-5p, hsa-miR-20a-5p, hsa-miR-222-3p, hsa-miR-24-3p, hsa-miR-3613-3p, hsa-miR-3178, hsa-miR-4505, hsa-miR-345-3p, hsa-miR-3648, and hsa-miR-455-3p) (P < 0.01). The qRT-PCR validation results demonstrated that hsa-miR-221-3p, hsa-miR-22-3p, hsa-miR-20a-5p, and hsa-miR-3613-3p were upregulated, while hsa-miR-3178 and hsa-miR-4505 were down-regulated. The softwares targetscan and miranda were further used to predict their target genes, and the gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis results showed that 20 GO terms and 20 KEGG pathways were significantly enriched. Our findings are the first to report expression profiling of miRNA and their functions in H5N1 AIV NS1-expressing HEK293 cells, and pave the way to further elucidating the accurate interaction mechanism between NS1 and virus replication, thus providing brand new insight into the prophylaxis and treatment of H5N1 AIV. |
format | Online Article Text |
id | pubmed-6830863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-68308632019-11-20 MicroRNA expression profiles from HEK293 cells expressing H5N1 avian influenza virus non-structural protein 1 Jiao, Hanwei Zheng, Zonglin Shuai, Xuehong Wu, Li Chen, Jixuan Luo, Yichen Zhao, Yu Wang, Hongjun Huang, Qingzhou Innate Immun Original Articles H5N1 avian influenza poses a serious threat to the poultry industry and human health. Non-structural protein 1 (NS1) plays an important role in the replication and pathogenesis of avian influenza virus (AIV). However, the function of the NS1 gene is still unclear. In this study, illumina genome analyzer iix screening was used to identify the differentially expressed microRNAs (miRNAs) in HEK293 cells expressing H5N1 AIV NS1. There were 13 differentially expressed miRNAs (hsa-miR-17-5p, hsa-miR-221-3p, hsa-miR-22-3p, hsa-miR-31-5p, hsa-miR-20a-5p, hsa-miR-222-3p, hsa-miR-24-3p, hsa-miR-3613-3p, hsa-miR-3178, hsa-miR-4505, hsa-miR-345-3p, hsa-miR-3648, and hsa-miR-455-3p) (P < 0.01). The qRT-PCR validation results demonstrated that hsa-miR-221-3p, hsa-miR-22-3p, hsa-miR-20a-5p, and hsa-miR-3613-3p were upregulated, while hsa-miR-3178 and hsa-miR-4505 were down-regulated. The softwares targetscan and miranda were further used to predict their target genes, and the gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis results showed that 20 GO terms and 20 KEGG pathways were significantly enriched. Our findings are the first to report expression profiling of miRNA and their functions in H5N1 AIV NS1-expressing HEK293 cells, and pave the way to further elucidating the accurate interaction mechanism between NS1 and virus replication, thus providing brand new insight into the prophylaxis and treatment of H5N1 AIV. SAGE Publications 2019-02-06 2019-02 /pmc/articles/PMC6830863/ /pubmed/30782044 http://dx.doi.org/10.1177/1753425919826342 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Articles Jiao, Hanwei Zheng, Zonglin Shuai, Xuehong Wu, Li Chen, Jixuan Luo, Yichen Zhao, Yu Wang, Hongjun Huang, Qingzhou MicroRNA expression profiles from HEK293 cells expressing H5N1 avian influenza virus non-structural protein 1 |
title | MicroRNA expression profiles from HEK293 cells expressing H5N1 avian
influenza virus non-structural protein 1 |
title_full | MicroRNA expression profiles from HEK293 cells expressing H5N1 avian
influenza virus non-structural protein 1 |
title_fullStr | MicroRNA expression profiles from HEK293 cells expressing H5N1 avian
influenza virus non-structural protein 1 |
title_full_unstemmed | MicroRNA expression profiles from HEK293 cells expressing H5N1 avian
influenza virus non-structural protein 1 |
title_short | MicroRNA expression profiles from HEK293 cells expressing H5N1 avian
influenza virus non-structural protein 1 |
title_sort | microrna expression profiles from hek293 cells expressing h5n1 avian
influenza virus non-structural protein 1 |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830863/ https://www.ncbi.nlm.nih.gov/pubmed/30782044 http://dx.doi.org/10.1177/1753425919826342 |
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