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DEMETER plant DNA demethylase induces antiviral response by interferon signalling in animal cells
DNA methylation is a prominent epigenetic modification in plants and animals regulated by similar mechanisms but the process of DNA demethylation is profoundly different. Unlike vertebrates that require a series of enzymatic conversions of 5-methylcytosine (5mC) into other bases for DNA demethylatio...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567224/ https://www.ncbi.nlm.nih.gov/pubmed/28831075 http://dx.doi.org/10.1038/s41598-017-08827-9 |
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author | Mok, Young Geun Choi, Ki Young Hong, Seung Hwan Huh, Jin Hoe |
author_facet | Mok, Young Geun Choi, Ki Young Hong, Seung Hwan Huh, Jin Hoe |
author_sort | Mok, Young Geun |
collection | PubMed |
description | DNA methylation is a prominent epigenetic modification in plants and animals regulated by similar mechanisms but the process of DNA demethylation is profoundly different. Unlike vertebrates that require a series of enzymatic conversions of 5-methylcytosine (5mC) into other bases for DNA demethylation, plants utilize the DEMETER (DME) family of 5mC DNA glycosylases to catalyze a direct removal of 5mC from DNA. Here we introduced Arabidopsis DME into human HEK-293T cells to allow direct 5mC excision, and observed that direct DNA demethylation activity was successfully implemented by DME expression. In addition, DME induced diverse cellular responses such as cell proliferation inhibition, cell cycle dysregulation and S phase arrest. Microarray and methylome analyses revealed that DME upregulated a number of genes including cell cycle components, heat shock proteins, and notably, various interferon-stimulated genes. Moreover, DME-mediated DNA demethylation activated endogenous repeat elements, which are likely to form dsRNAs as viral mimics and eventually trigger interferon cascades to establish the antiviral state. This work demonstrates that plant DNA demethylase catalyzes DNA demethylation with a bypass of initial base conversion steps, and the interferon signaling plays a pivotal role to alleviate genotoxic stresses associated with DME-induced DNA demethylation in mammalian cells. |
format | Online Article Text |
id | pubmed-5567224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55672242017-09-01 DEMETER plant DNA demethylase induces antiviral response by interferon signalling in animal cells Mok, Young Geun Choi, Ki Young Hong, Seung Hwan Huh, Jin Hoe Sci Rep Article DNA methylation is a prominent epigenetic modification in plants and animals regulated by similar mechanisms but the process of DNA demethylation is profoundly different. Unlike vertebrates that require a series of enzymatic conversions of 5-methylcytosine (5mC) into other bases for DNA demethylation, plants utilize the DEMETER (DME) family of 5mC DNA glycosylases to catalyze a direct removal of 5mC from DNA. Here we introduced Arabidopsis DME into human HEK-293T cells to allow direct 5mC excision, and observed that direct DNA demethylation activity was successfully implemented by DME expression. In addition, DME induced diverse cellular responses such as cell proliferation inhibition, cell cycle dysregulation and S phase arrest. Microarray and methylome analyses revealed that DME upregulated a number of genes including cell cycle components, heat shock proteins, and notably, various interferon-stimulated genes. Moreover, DME-mediated DNA demethylation activated endogenous repeat elements, which are likely to form dsRNAs as viral mimics and eventually trigger interferon cascades to establish the antiviral state. This work demonstrates that plant DNA demethylase catalyzes DNA demethylation with a bypass of initial base conversion steps, and the interferon signaling plays a pivotal role to alleviate genotoxic stresses associated with DME-induced DNA demethylation in mammalian cells. Nature Publishing Group UK 2017-08-22 /pmc/articles/PMC5567224/ /pubmed/28831075 http://dx.doi.org/10.1038/s41598-017-08827-9 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Mok, Young Geun Choi, Ki Young Hong, Seung Hwan Huh, Jin Hoe DEMETER plant DNA demethylase induces antiviral response by interferon signalling in animal cells |
title | DEMETER plant DNA demethylase induces antiviral response by interferon signalling in animal cells |
title_full | DEMETER plant DNA demethylase induces antiviral response by interferon signalling in animal cells |
title_fullStr | DEMETER plant DNA demethylase induces antiviral response by interferon signalling in animal cells |
title_full_unstemmed | DEMETER plant DNA demethylase induces antiviral response by interferon signalling in animal cells |
title_short | DEMETER plant DNA demethylase induces antiviral response by interferon signalling in animal cells |
title_sort | demeter plant dna demethylase induces antiviral response by interferon signalling in animal cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567224/ https://www.ncbi.nlm.nih.gov/pubmed/28831075 http://dx.doi.org/10.1038/s41598-017-08827-9 |
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