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H2A.B facilitates transcription elongation at methylated CpG loci
H2A.B is a unique histone H2A variant that only exists in mammals. Here we found that H2A.B is ubiquitously expressed in major organs. Genome-wide analysis of H2A.B in mouse ES cells shows that H2A.B is associated with methylated DNA in gene body regions. Moreover, H2A.B-enriched gene loci are activ...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975057/ https://www.ncbi.nlm.nih.gov/pubmed/24402521 http://dx.doi.org/10.1101/gr.156877.113 |
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author | Chen, Yibin Chen, Qiang McEachin, Richard C. Cavalcoli, James D. Yu, Xiaochun |
author_facet | Chen, Yibin Chen, Qiang McEachin, Richard C. Cavalcoli, James D. Yu, Xiaochun |
author_sort | Chen, Yibin |
collection | PubMed |
description | H2A.B is a unique histone H2A variant that only exists in mammals. Here we found that H2A.B is ubiquitously expressed in major organs. Genome-wide analysis of H2A.B in mouse ES cells shows that H2A.B is associated with methylated DNA in gene body regions. Moreover, H2A.B-enriched gene loci are actively transcribed. One typical example is that H2A.B is enriched in a set of differentially methylated regions at imprinted loci and facilitates transcription elongation. These results suggest that H2A.B positively regulates transcription elongation by overcoming DNA methylation in the transcribed region. It provides a novel mechanism by which transcription is regulated at DNA hypermethylated regions. |
format | Online Article Text |
id | pubmed-3975057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39750572014-10-01 H2A.B facilitates transcription elongation at methylated CpG loci Chen, Yibin Chen, Qiang McEachin, Richard C. Cavalcoli, James D. Yu, Xiaochun Genome Res Research H2A.B is a unique histone H2A variant that only exists in mammals. Here we found that H2A.B is ubiquitously expressed in major organs. Genome-wide analysis of H2A.B in mouse ES cells shows that H2A.B is associated with methylated DNA in gene body regions. Moreover, H2A.B-enriched gene loci are actively transcribed. One typical example is that H2A.B is enriched in a set of differentially methylated regions at imprinted loci and facilitates transcription elongation. These results suggest that H2A.B positively regulates transcription elongation by overcoming DNA methylation in the transcribed region. It provides a novel mechanism by which transcription is regulated at DNA hypermethylated regions. Cold Spring Harbor Laboratory Press 2014-04 /pmc/articles/PMC3975057/ /pubmed/24402521 http://dx.doi.org/10.1101/gr.156877.113 Text en © 2014 Chen et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported), as described at http://creativecommons.org/licenses/by-nc/3.0/. |
spellingShingle | Research Chen, Yibin Chen, Qiang McEachin, Richard C. Cavalcoli, James D. Yu, Xiaochun H2A.B facilitates transcription elongation at methylated CpG loci |
title | H2A.B facilitates transcription elongation at methylated CpG loci |
title_full | H2A.B facilitates transcription elongation at methylated CpG loci |
title_fullStr | H2A.B facilitates transcription elongation at methylated CpG loci |
title_full_unstemmed | H2A.B facilitates transcription elongation at methylated CpG loci |
title_short | H2A.B facilitates transcription elongation at methylated CpG loci |
title_sort | h2a.b facilitates transcription elongation at methylated cpg loci |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975057/ https://www.ncbi.nlm.nih.gov/pubmed/24402521 http://dx.doi.org/10.1101/gr.156877.113 |
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