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Epigenetic Control of Cytomegalovirus Latency and Reactivation

Cytomegalovirus (CMV) gene expression is repressed in latency due to heterochromatinization of viral genomes. In murine CMV (MCMV) latently infected mice, viral genomes are bound to histones with heterochromatic modifications, to enzymes that mediate these modifications, and to adaptor proteins that...

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Autores principales: Liu, Xue-feng, Wang, Xueqiong, Yan, Shixian, Zhang, Zheng, Abecassis, Michael, Hummel, Mary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3712310/
https://www.ncbi.nlm.nih.gov/pubmed/23698401
http://dx.doi.org/10.3390/v5051325
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author Liu, Xue-feng
Wang, Xueqiong
Yan, Shixian
Zhang, Zheng
Abecassis, Michael
Hummel, Mary
author_facet Liu, Xue-feng
Wang, Xueqiong
Yan, Shixian
Zhang, Zheng
Abecassis, Michael
Hummel, Mary
author_sort Liu, Xue-feng
collection PubMed
description Cytomegalovirus (CMV) gene expression is repressed in latency due to heterochromatinization of viral genomes. In murine CMV (MCMV) latently infected mice, viral genomes are bound to histones with heterochromatic modifications, to enzymes that mediate these modifications, and to adaptor proteins that may recruit co-repressor complexes. Kinetic analyses of repressor binding show that these repressors are recruited at the earliest time of infection, suggesting that latency may be the default state. Kidney transplantation leads to epigenetic reprogramming of latent viral chromatin and reactivation of immediate early gene expression. Inflammatory signaling pathways, which activate transcription factors that regulate the major immediate early promoter (MIEP), likely mediate the switch in viral chromatin.
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spelling pubmed-37123102013-07-16 Epigenetic Control of Cytomegalovirus Latency and Reactivation Liu, Xue-feng Wang, Xueqiong Yan, Shixian Zhang, Zheng Abecassis, Michael Hummel, Mary Viruses Communication Cytomegalovirus (CMV) gene expression is repressed in latency due to heterochromatinization of viral genomes. In murine CMV (MCMV) latently infected mice, viral genomes are bound to histones with heterochromatic modifications, to enzymes that mediate these modifications, and to adaptor proteins that may recruit co-repressor complexes. Kinetic analyses of repressor binding show that these repressors are recruited at the earliest time of infection, suggesting that latency may be the default state. Kidney transplantation leads to epigenetic reprogramming of latent viral chromatin and reactivation of immediate early gene expression. Inflammatory signaling pathways, which activate transcription factors that regulate the major immediate early promoter (MIEP), likely mediate the switch in viral chromatin. MDPI 2013-05-23 /pmc/articles/PMC3712310/ /pubmed/23698401 http://dx.doi.org/10.3390/v5051325 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Communication
Liu, Xue-feng
Wang, Xueqiong
Yan, Shixian
Zhang, Zheng
Abecassis, Michael
Hummel, Mary
Epigenetic Control of Cytomegalovirus Latency and Reactivation
title Epigenetic Control of Cytomegalovirus Latency and Reactivation
title_full Epigenetic Control of Cytomegalovirus Latency and Reactivation
title_fullStr Epigenetic Control of Cytomegalovirus Latency and Reactivation
title_full_unstemmed Epigenetic Control of Cytomegalovirus Latency and Reactivation
title_short Epigenetic Control of Cytomegalovirus Latency and Reactivation
title_sort epigenetic control of cytomegalovirus latency and reactivation
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3712310/
https://www.ncbi.nlm.nih.gov/pubmed/23698401
http://dx.doi.org/10.3390/v5051325
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