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DNA methylation immediately adjacent to active histone marking does not silence transcription

Active promoters generally contain histone H3/H4 hyperacetylation and tri-methylation at H3 lysine 4, whereas repressed promoters are associated with DNA methylation. Here we show that the repressed erythroid-specific carbonic anhydrase II (CAII) promoter has active histone modifications localized a...

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Autores principales: Brinkman, Arie B., Pennings, Sebastiaan W. C., Braliou, Georgia G., Rietveld, Luc E. G., Stunnenberg, Hendrik G.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1807972/
https://www.ncbi.nlm.nih.gov/pubmed/17202157
http://dx.doi.org/10.1093/nar/gkl1014
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author Brinkman, Arie B.
Pennings, Sebastiaan W. C.
Braliou, Georgia G.
Rietveld, Luc E. G.
Stunnenberg, Hendrik G.
author_facet Brinkman, Arie B.
Pennings, Sebastiaan W. C.
Braliou, Georgia G.
Rietveld, Luc E. G.
Stunnenberg, Hendrik G.
author_sort Brinkman, Arie B.
collection PubMed
description Active promoters generally contain histone H3/H4 hyperacetylation and tri-methylation at H3 lysine 4, whereas repressed promoters are associated with DNA methylation. Here we show that the repressed erythroid-specific carbonic anhydrase II (CAII) promoter has active histone modifications localized around the transcription start, while high levels of CpG methylation are present directly upstream from these active marks. Despite the presence of active histone modifications, the repressed promoter requires hormone-induced activation for efficient preinitiation complex assembly. Transient and positional changes in histone H3/H4 acetylation and local changes in nucleosome density are evident during activation, but the bipartite epigenetic code is stably maintained. Our results suggest that active histone modifications may prevent spreading of CpG methylation towards the promoter and show that repressive DNA methylation immediately adjacent to a promoter does not necessarily repress transcription.
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spelling pubmed-18079722007-03-02 DNA methylation immediately adjacent to active histone marking does not silence transcription Brinkman, Arie B. Pennings, Sebastiaan W. C. Braliou, Georgia G. Rietveld, Luc E. G. Stunnenberg, Hendrik G. Nucleic Acids Res Molecular Biology Active promoters generally contain histone H3/H4 hyperacetylation and tri-methylation at H3 lysine 4, whereas repressed promoters are associated with DNA methylation. Here we show that the repressed erythroid-specific carbonic anhydrase II (CAII) promoter has active histone modifications localized around the transcription start, while high levels of CpG methylation are present directly upstream from these active marks. Despite the presence of active histone modifications, the repressed promoter requires hormone-induced activation for efficient preinitiation complex assembly. Transient and positional changes in histone H3/H4 acetylation and local changes in nucleosome density are evident during activation, but the bipartite epigenetic code is stably maintained. Our results suggest that active histone modifications may prevent spreading of CpG methylation towards the promoter and show that repressive DNA methylation immediately adjacent to a promoter does not necessarily repress transcription. Oxford University Press 2007-02 2007-01-03 /pmc/articles/PMC1807972/ /pubmed/17202157 http://dx.doi.org/10.1093/nar/gkl1014 Text en © 2006 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Brinkman, Arie B.
Pennings, Sebastiaan W. C.
Braliou, Georgia G.
Rietveld, Luc E. G.
Stunnenberg, Hendrik G.
DNA methylation immediately adjacent to active histone marking does not silence transcription
title DNA methylation immediately adjacent to active histone marking does not silence transcription
title_full DNA methylation immediately adjacent to active histone marking does not silence transcription
title_fullStr DNA methylation immediately adjacent to active histone marking does not silence transcription
title_full_unstemmed DNA methylation immediately adjacent to active histone marking does not silence transcription
title_short DNA methylation immediately adjacent to active histone marking does not silence transcription
title_sort dna methylation immediately adjacent to active histone marking does not silence transcription
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1807972/
https://www.ncbi.nlm.nih.gov/pubmed/17202157
http://dx.doi.org/10.1093/nar/gkl1014
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