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Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates

Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive effects of DNA methylation on chromatin. In cold-blooded vertebrates, computational CGI predictions often reside away from gene promoters, suggesting...

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Autores principales: Long, Hannah K, Sims, David, Heger, Andreas, Blackledge, Neil P, Kutter, Claudia, Wright, Megan L, Grützner, Frank, Odom, Duncan T, Patient, Roger, Ponting, Chris P, Klose, Robert J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583005/
https://www.ncbi.nlm.nih.gov/pubmed/23467541
http://dx.doi.org/10.7554/eLife.00348
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author Long, Hannah K
Sims, David
Heger, Andreas
Blackledge, Neil P
Kutter, Claudia
Wright, Megan L
Grützner, Frank
Odom, Duncan T
Patient, Roger
Ponting, Chris P
Klose, Robert J
author_facet Long, Hannah K
Sims, David
Heger, Andreas
Blackledge, Neil P
Kutter, Claudia
Wright, Megan L
Grützner, Frank
Odom, Duncan T
Patient, Roger
Ponting, Chris P
Klose, Robert J
author_sort Long, Hannah K
collection PubMed
description Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive effects of DNA methylation on chromatin. In cold-blooded vertebrates, computational CGI predictions often reside away from gene promoters, suggesting a major divergence in gene promoter architecture across vertebrates. By experimentally identifying non-methylated DNA in the genomes of seven diverse vertebrates, we instead reveal that non-methylated islands (NMIs) of DNA are a central feature of vertebrate gene promoters. Furthermore, NMIs are present at orthologous genes across vast evolutionary distances, revealing a surprising level of conservation in this epigenetic feature. By profiling NMIs in different tissues and developmental stages we uncover a unifying set of features that are central to the function of NMIs in vertebrates. Together these findings demonstrate an ancient logic for NMI usage at gene promoters and reveal an unprecedented level of epigenetic conservation across vertebrate evolution. DOI: http://dx.doi.org/10.7554/eLife.00348.001
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spelling pubmed-35830052013-03-05 Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates Long, Hannah K Sims, David Heger, Andreas Blackledge, Neil P Kutter, Claudia Wright, Megan L Grützner, Frank Odom, Duncan T Patient, Roger Ponting, Chris P Klose, Robert J eLife Genes and Chromosomes Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive effects of DNA methylation on chromatin. In cold-blooded vertebrates, computational CGI predictions often reside away from gene promoters, suggesting a major divergence in gene promoter architecture across vertebrates. By experimentally identifying non-methylated DNA in the genomes of seven diverse vertebrates, we instead reveal that non-methylated islands (NMIs) of DNA are a central feature of vertebrate gene promoters. Furthermore, NMIs are present at orthologous genes across vast evolutionary distances, revealing a surprising level of conservation in this epigenetic feature. By profiling NMIs in different tissues and developmental stages we uncover a unifying set of features that are central to the function of NMIs in vertebrates. Together these findings demonstrate an ancient logic for NMI usage at gene promoters and reveal an unprecedented level of epigenetic conservation across vertebrate evolution. DOI: http://dx.doi.org/10.7554/eLife.00348.001 eLife Sciences Publications, Ltd 2013-02-26 /pmc/articles/PMC3583005/ /pubmed/23467541 http://dx.doi.org/10.7554/eLife.00348 Text en Copyright © 2013, Long et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Genes and Chromosomes
Long, Hannah K
Sims, David
Heger, Andreas
Blackledge, Neil P
Kutter, Claudia
Wright, Megan L
Grützner, Frank
Odom, Duncan T
Patient, Roger
Ponting, Chris P
Klose, Robert J
Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates
title Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates
title_full Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates
title_fullStr Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates
title_full_unstemmed Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates
title_short Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates
title_sort epigenetic conservation at gene regulatory elements revealed by non-methylated dna profiling in seven vertebrates
topic Genes and Chromosomes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583005/
https://www.ncbi.nlm.nih.gov/pubmed/23467541
http://dx.doi.org/10.7554/eLife.00348
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