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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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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. |
format | Online Article Text |
id | pubmed-3712310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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