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Dynamic chromatin accessibility profiling reveals changes in host genome organization in response to baculovirus infection
DNA viruses can hijack and manipulate the host chromatin state to facilitate their infection. Multiple lines of evidences reveal that DNA virus infection results in the host chromatin relocation, yet there is little known about the effects of viral infection on the architecture of host chromatin. He...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7326278/ https://www.ncbi.nlm.nih.gov/pubmed/32511266 http://dx.doi.org/10.1371/journal.ppat.1008633 |
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author | Kong, Xiangshuo Wei, Guisheng Chen, Nan Zhao, Shudi Shen, Yunwang Zhang, Jianjia Li, Yang Zeng, Xiaoqun Wu, Xiaofeng |
author_facet | Kong, Xiangshuo Wei, Guisheng Chen, Nan Zhao, Shudi Shen, Yunwang Zhang, Jianjia Li, Yang Zeng, Xiaoqun Wu, Xiaofeng |
author_sort | Kong, Xiangshuo |
collection | PubMed |
description | DNA viruses can hijack and manipulate the host chromatin state to facilitate their infection. Multiple lines of evidences reveal that DNA virus infection results in the host chromatin relocation, yet there is little known about the effects of viral infection on the architecture of host chromatin. Here, a combination of epigenomic, transcriptomic and biochemical assays were conducted to investigate the temporal dynamics of chromatin accessibility in response to Bombyx mori nucleopolyhedrovirus (BmNPV) infection. The high-quality ATAC-seq data indicated that progressive chromatin remodeling took place following BmNPV infection. Viral infection resulted in a more open chromatin architecture, along with the marginalization of host genome and nucleosome disassembly. Moreover, our results revealed that chromatin accessibility in uninfected cells was regulated by euchromatic modifications, whereas the viral-induced highly accessible chromatin regions were originally associated with facultative heterochromatic modification. Overall, our findings illustrate for the first time the organization and accessibility of host chromatin in BmNPV-infected cells, which lay the foundation for future studies on epigenomic regulation mediated by DNA viruses. |
format | Online Article Text |
id | pubmed-7326278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-73262782020-07-10 Dynamic chromatin accessibility profiling reveals changes in host genome organization in response to baculovirus infection Kong, Xiangshuo Wei, Guisheng Chen, Nan Zhao, Shudi Shen, Yunwang Zhang, Jianjia Li, Yang Zeng, Xiaoqun Wu, Xiaofeng PLoS Pathog Research Article DNA viruses can hijack and manipulate the host chromatin state to facilitate their infection. Multiple lines of evidences reveal that DNA virus infection results in the host chromatin relocation, yet there is little known about the effects of viral infection on the architecture of host chromatin. Here, a combination of epigenomic, transcriptomic and biochemical assays were conducted to investigate the temporal dynamics of chromatin accessibility in response to Bombyx mori nucleopolyhedrovirus (BmNPV) infection. The high-quality ATAC-seq data indicated that progressive chromatin remodeling took place following BmNPV infection. Viral infection resulted in a more open chromatin architecture, along with the marginalization of host genome and nucleosome disassembly. Moreover, our results revealed that chromatin accessibility in uninfected cells was regulated by euchromatic modifications, whereas the viral-induced highly accessible chromatin regions were originally associated with facultative heterochromatic modification. Overall, our findings illustrate for the first time the organization and accessibility of host chromatin in BmNPV-infected cells, which lay the foundation for future studies on epigenomic regulation mediated by DNA viruses. Public Library of Science 2020-06-08 /pmc/articles/PMC7326278/ /pubmed/32511266 http://dx.doi.org/10.1371/journal.ppat.1008633 Text en © 2020 Kong et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kong, Xiangshuo Wei, Guisheng Chen, Nan Zhao, Shudi Shen, Yunwang Zhang, Jianjia Li, Yang Zeng, Xiaoqun Wu, Xiaofeng Dynamic chromatin accessibility profiling reveals changes in host genome organization in response to baculovirus infection |
title | Dynamic chromatin accessibility profiling reveals changes in host genome organization in response to baculovirus infection |
title_full | Dynamic chromatin accessibility profiling reveals changes in host genome organization in response to baculovirus infection |
title_fullStr | Dynamic chromatin accessibility profiling reveals changes in host genome organization in response to baculovirus infection |
title_full_unstemmed | Dynamic chromatin accessibility profiling reveals changes in host genome organization in response to baculovirus infection |
title_short | Dynamic chromatin accessibility profiling reveals changes in host genome organization in response to baculovirus infection |
title_sort | dynamic chromatin accessibility profiling reveals changes in host genome organization in response to baculovirus infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7326278/ https://www.ncbi.nlm.nih.gov/pubmed/32511266 http://dx.doi.org/10.1371/journal.ppat.1008633 |
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