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Transcriptome altered by latent human cytomegalovirus infection on THP-1 cells using RNA-seq
Human cytomegalovirus (HCMV) has been recognized as a cause of severe, sometimes life-threatening disease in congenitally infected newborns as well as in immunocompromised individuals. However, the molecular mechanisms of the host-virus interaction remain poorly understood. Here, we profiled the exp...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126988/ https://www.ncbi.nlm.nih.gov/pubmed/27623506 http://dx.doi.org/10.1016/j.gene.2016.09.014 |
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author | Zhang, Qi Lai, Mei-Mei Lou, Yun-Yan Guo, Bin-Han Wang, Hui-Yan Zheng, Xiao-Qun |
author_facet | Zhang, Qi Lai, Mei-Mei Lou, Yun-Yan Guo, Bin-Han Wang, Hui-Yan Zheng, Xiao-Qun |
author_sort | Zhang, Qi |
collection | PubMed |
description | Human cytomegalovirus (HCMV) has been recognized as a cause of severe, sometimes life-threatening disease in congenitally infected newborns as well as in immunocompromised individuals. However, the molecular mechanisms of the host-virus interaction remain poorly understood. Here, we profiled the expression of mRNAs and long noncoding RNAs (lncRNAs) in THP-1 cells using the emerging RNA-seq to investigate the transcriptional changes during HCMV latent infection. At 4 days post HCMV infection, a total of 169,008,624 sequence reads and 180,616 transcripts were obtained, respectively. Of these transcripts, 1,354 noncoding genes and 12,952 protein-coding genes were observed in Refseq database. Differential gene expression analysis identified 2,153 differentially expressed genes (DEGs) between HCMV-infected and mock-infected THP-1 cells, including 1,098 up-regulated genes and 1,055 down-regulated genes. These regulated genes were involved in pathways of apoptosis, inflammatory response and cell cycle progression, all of which may be implicated in viral pathogenesis. In addition, 646 lncRNAs (208 known lncRNAs and 438 novel lncRNAs) were upregulated and 424 (140 known and 284 novel) were downregulated in infected THP-1 cells. These findings have provided a dynamic scenario of DE candidate genes and lncRNAs at the virus-host interface and clearly warrant further experimental investigation associated with HCMV infection. |
format | Online Article Text |
id | pubmed-7126988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71269882020-04-08 Transcriptome altered by latent human cytomegalovirus infection on THP-1 cells using RNA-seq Zhang, Qi Lai, Mei-Mei Lou, Yun-Yan Guo, Bin-Han Wang, Hui-Yan Zheng, Xiao-Qun Gene Research Paper Human cytomegalovirus (HCMV) has been recognized as a cause of severe, sometimes life-threatening disease in congenitally infected newborns as well as in immunocompromised individuals. However, the molecular mechanisms of the host-virus interaction remain poorly understood. Here, we profiled the expression of mRNAs and long noncoding RNAs (lncRNAs) in THP-1 cells using the emerging RNA-seq to investigate the transcriptional changes during HCMV latent infection. At 4 days post HCMV infection, a total of 169,008,624 sequence reads and 180,616 transcripts were obtained, respectively. Of these transcripts, 1,354 noncoding genes and 12,952 protein-coding genes were observed in Refseq database. Differential gene expression analysis identified 2,153 differentially expressed genes (DEGs) between HCMV-infected and mock-infected THP-1 cells, including 1,098 up-regulated genes and 1,055 down-regulated genes. These regulated genes were involved in pathways of apoptosis, inflammatory response and cell cycle progression, all of which may be implicated in viral pathogenesis. In addition, 646 lncRNAs (208 known lncRNAs and 438 novel lncRNAs) were upregulated and 424 (140 known and 284 novel) were downregulated in infected THP-1 cells. These findings have provided a dynamic scenario of DE candidate genes and lncRNAs at the virus-host interface and clearly warrant further experimental investigation associated with HCMV infection. Elsevier B.V. 2016-12-05 2016-09-10 /pmc/articles/PMC7126988/ /pubmed/27623506 http://dx.doi.org/10.1016/j.gene.2016.09.014 Text en © 2016 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Research Paper Zhang, Qi Lai, Mei-Mei Lou, Yun-Yan Guo, Bin-Han Wang, Hui-Yan Zheng, Xiao-Qun Transcriptome altered by latent human cytomegalovirus infection on THP-1 cells using RNA-seq |
title | Transcriptome altered by latent human cytomegalovirus infection on THP-1 cells using RNA-seq |
title_full | Transcriptome altered by latent human cytomegalovirus infection on THP-1 cells using RNA-seq |
title_fullStr | Transcriptome altered by latent human cytomegalovirus infection on THP-1 cells using RNA-seq |
title_full_unstemmed | Transcriptome altered by latent human cytomegalovirus infection on THP-1 cells using RNA-seq |
title_short | Transcriptome altered by latent human cytomegalovirus infection on THP-1 cells using RNA-seq |
title_sort | transcriptome altered by latent human cytomegalovirus infection on thp-1 cells using rna-seq |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126988/ https://www.ncbi.nlm.nih.gov/pubmed/27623506 http://dx.doi.org/10.1016/j.gene.2016.09.014 |
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