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Identification of DNA methylation regulated novel host genes relevant to inhibition of virus replication in porcine PK15 cell using double stranded RNA mimics and DNA methyltransferase inhibitor

During RNA viruses's replication, double-stranded RNA (dsRNA) is normally produced and induce host innate immune response. Most of gene activation due cytokine mediated but which are due to methylation mediated is still unknown. In the study, DNA methylome was integrated with our previous trans...

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Autores principales: Wang, Xiaoshuo, Ao, Hong, Song, Minyan, Bai, Lijing, He, Weiyong, Wang, Chuduan, Yu, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125705/
https://www.ncbi.nlm.nih.gov/pubmed/30315899
http://dx.doi.org/10.1016/j.ygeno.2018.09.020
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author Wang, Xiaoshuo
Ao, Hong
Song, Minyan
Bai, Lijing
He, Weiyong
Wang, Chuduan
Yu, Ying
author_facet Wang, Xiaoshuo
Ao, Hong
Song, Minyan
Bai, Lijing
He, Weiyong
Wang, Chuduan
Yu, Ying
author_sort Wang, Xiaoshuo
collection PubMed
description During RNA viruses's replication, double-stranded RNA (dsRNA) is normally produced and induce host innate immune response. Most of gene activation due cytokine mediated but which are due to methylation mediated is still unknown. In the study, DNA methylome was integrated with our previous transcriptome data to investigate the differentially methylated regions and genes using MeDIP-chip technology. We found that the transcriptional expressions of 15, 37 and 18 genes were negatively related with their promoter DNA methylation levels in the cells treated by PolyI:C, Aza-CdR, as well as PolyI:C plus Aza-CdR, respectively, compared with the untreated cells. GO analysis revealed hypo-methylated genes (BNIP3L and CDK9) and a hyper-methylated gene (ZC3HAV1) involved in the host response to viral replication. Our results suggest that these novel genes targeted by DNA methylation can be potential markers relevant to virus replication and host innate immune response to set up a medical model of infectious diseases.
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spelling pubmed-71257052020-04-08 Identification of DNA methylation regulated novel host genes relevant to inhibition of virus replication in porcine PK15 cell using double stranded RNA mimics and DNA methyltransferase inhibitor Wang, Xiaoshuo Ao, Hong Song, Minyan Bai, Lijing He, Weiyong Wang, Chuduan Yu, Ying Genomics Article During RNA viruses's replication, double-stranded RNA (dsRNA) is normally produced and induce host innate immune response. Most of gene activation due cytokine mediated but which are due to methylation mediated is still unknown. In the study, DNA methylome was integrated with our previous transcriptome data to investigate the differentially methylated regions and genes using MeDIP-chip technology. We found that the transcriptional expressions of 15, 37 and 18 genes were negatively related with their promoter DNA methylation levels in the cells treated by PolyI:C, Aza-CdR, as well as PolyI:C plus Aza-CdR, respectively, compared with the untreated cells. GO analysis revealed hypo-methylated genes (BNIP3L and CDK9) and a hyper-methylated gene (ZC3HAV1) involved in the host response to viral replication. Our results suggest that these novel genes targeted by DNA methylation can be potential markers relevant to virus replication and host innate immune response to set up a medical model of infectious diseases. Published by Elsevier Inc. 2019-12 2018-10-11 /pmc/articles/PMC7125705/ /pubmed/30315899 http://dx.doi.org/10.1016/j.ygeno.2018.09.020 Text en © 2018 Published by Elsevier Inc. 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 Article
Wang, Xiaoshuo
Ao, Hong
Song, Minyan
Bai, Lijing
He, Weiyong
Wang, Chuduan
Yu, Ying
Identification of DNA methylation regulated novel host genes relevant to inhibition of virus replication in porcine PK15 cell using double stranded RNA mimics and DNA methyltransferase inhibitor
title Identification of DNA methylation regulated novel host genes relevant to inhibition of virus replication in porcine PK15 cell using double stranded RNA mimics and DNA methyltransferase inhibitor
title_full Identification of DNA methylation regulated novel host genes relevant to inhibition of virus replication in porcine PK15 cell using double stranded RNA mimics and DNA methyltransferase inhibitor
title_fullStr Identification of DNA methylation regulated novel host genes relevant to inhibition of virus replication in porcine PK15 cell using double stranded RNA mimics and DNA methyltransferase inhibitor
title_full_unstemmed Identification of DNA methylation regulated novel host genes relevant to inhibition of virus replication in porcine PK15 cell using double stranded RNA mimics and DNA methyltransferase inhibitor
title_short Identification of DNA methylation regulated novel host genes relevant to inhibition of virus replication in porcine PK15 cell using double stranded RNA mimics and DNA methyltransferase inhibitor
title_sort identification of dna methylation regulated novel host genes relevant to inhibition of virus replication in porcine pk15 cell using double stranded rna mimics and dna methyltransferase inhibitor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125705/
https://www.ncbi.nlm.nih.gov/pubmed/30315899
http://dx.doi.org/10.1016/j.ygeno.2018.09.020
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