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DNA Methylation Fluctuation Induced by Virus Infection Differs between MD-resistant and -susceptible Chickens

Marek’s disease (MD) is a lymphoproliferative disease induced by Marek’s disease virus (MDV) infection. To augment vaccination measures in MD control, host genetic resistant to MD becomes obviously more and more important. To elucidate the mechanism of MD-resistance, most of researches were focused...

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Autores principales: Luo, Juan, Yu, Ying, Chang, Shuang, Tian, Fei, Zhang, Huanmin, Song, Jiuzhou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281210/
https://www.ncbi.nlm.nih.gov/pubmed/22363343
http://dx.doi.org/10.3389/fgene.2012.00020
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author Luo, Juan
Yu, Ying
Chang, Shuang
Tian, Fei
Zhang, Huanmin
Song, Jiuzhou
author_facet Luo, Juan
Yu, Ying
Chang, Shuang
Tian, Fei
Zhang, Huanmin
Song, Jiuzhou
author_sort Luo, Juan
collection PubMed
description Marek’s disease (MD) is a lymphoproliferative disease induced by Marek’s disease virus (MDV) infection. To augment vaccination measures in MD control, host genetic resistant to MD becomes obviously more and more important. To elucidate the mechanism of MD-resistance, most of researches were focused on the genetic differences between resistant and susceptible chickens. However, epigenetic features between MD resistant and susceptible chickens are poorly characterized. Using bisulfite pyrosequencing method, we found some candidate genes have higher promoter methylation in the MD-susceptible (L7(2)) chickens than in the MD-resistant (L6(3)) chickens. The hypermethylated genes, involved in cellular component organization, responding to stimulus, cell adhesion, and immune system process, may play important role in susceptibility to disease by deregulation of these genes. MDV infection induced the expression changes of all three methyltransferases genes (DNMT1, DNMT3a, and DNMT3b) in both lines of chickens. The DNMT1 was up-regulated in L7(2), whereas the DNMT3b was down-regulated in L6(3) at 21 dpi. Interestingly, a dynamic change of promoter methylation was observed during MDV life cycle. Some genes, including HDAC9, GH, STAT1, CIITA, FABP3, LATS2, and H2Ac, showed differential methylation behaviors between the two lines of chickens. In summary, the findings from this study suggested that DNA methylation heterogeneity and MDV infection induced methylation alterations differences existed between the two lines of chickens. Therefore, it is suggested that epigenetic mechanisms may be involved in modulating the resistance and/or susceptibility to MD in chickens.
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spelling pubmed-32812102012-02-23 DNA Methylation Fluctuation Induced by Virus Infection Differs between MD-resistant and -susceptible Chickens Luo, Juan Yu, Ying Chang, Shuang Tian, Fei Zhang, Huanmin Song, Jiuzhou Front Genet Genetics Marek’s disease (MD) is a lymphoproliferative disease induced by Marek’s disease virus (MDV) infection. To augment vaccination measures in MD control, host genetic resistant to MD becomes obviously more and more important. To elucidate the mechanism of MD-resistance, most of researches were focused on the genetic differences between resistant and susceptible chickens. However, epigenetic features between MD resistant and susceptible chickens are poorly characterized. Using bisulfite pyrosequencing method, we found some candidate genes have higher promoter methylation in the MD-susceptible (L7(2)) chickens than in the MD-resistant (L6(3)) chickens. The hypermethylated genes, involved in cellular component organization, responding to stimulus, cell adhesion, and immune system process, may play important role in susceptibility to disease by deregulation of these genes. MDV infection induced the expression changes of all three methyltransferases genes (DNMT1, DNMT3a, and DNMT3b) in both lines of chickens. The DNMT1 was up-regulated in L7(2), whereas the DNMT3b was down-regulated in L6(3) at 21 dpi. Interestingly, a dynamic change of promoter methylation was observed during MDV life cycle. Some genes, including HDAC9, GH, STAT1, CIITA, FABP3, LATS2, and H2Ac, showed differential methylation behaviors between the two lines of chickens. In summary, the findings from this study suggested that DNA methylation heterogeneity and MDV infection induced methylation alterations differences existed between the two lines of chickens. Therefore, it is suggested that epigenetic mechanisms may be involved in modulating the resistance and/or susceptibility to MD in chickens. Frontiers Research Foundation 2012-02-17 /pmc/articles/PMC3281210/ /pubmed/22363343 http://dx.doi.org/10.3389/fgene.2012.00020 Text en Copyright © 2012 Luo, Yu, Chang, Tian, Zhang and Song. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Genetics
Luo, Juan
Yu, Ying
Chang, Shuang
Tian, Fei
Zhang, Huanmin
Song, Jiuzhou
DNA Methylation Fluctuation Induced by Virus Infection Differs between MD-resistant and -susceptible Chickens
title DNA Methylation Fluctuation Induced by Virus Infection Differs between MD-resistant and -susceptible Chickens
title_full DNA Methylation Fluctuation Induced by Virus Infection Differs between MD-resistant and -susceptible Chickens
title_fullStr DNA Methylation Fluctuation Induced by Virus Infection Differs between MD-resistant and -susceptible Chickens
title_full_unstemmed DNA Methylation Fluctuation Induced by Virus Infection Differs between MD-resistant and -susceptible Chickens
title_short DNA Methylation Fluctuation Induced by Virus Infection Differs between MD-resistant and -susceptible Chickens
title_sort dna methylation fluctuation induced by virus infection differs between md-resistant and -susceptible chickens
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281210/
https://www.ncbi.nlm.nih.gov/pubmed/22363343
http://dx.doi.org/10.3389/fgene.2012.00020
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