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5-hydroxymethylcytosine is highly dynamic across human fetal brain development

BACKGROUND: Epigenetic processes play a key role in orchestrating transcriptional regulation during the development of the human central nervous system. We previously described dynamic changes in DNA methylation (5mC) occurring during human fetal brain development, but other epigenetic processes ope...

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Autores principales: Spiers, Helen, Hannon, Eilis, Schalkwyk, Leonard C., Bray, Nicholas J., Mill, Jonathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604137/
https://www.ncbi.nlm.nih.gov/pubmed/28923016
http://dx.doi.org/10.1186/s12864-017-4091-x
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author Spiers, Helen
Hannon, Eilis
Schalkwyk, Leonard C.
Bray, Nicholas J.
Mill, Jonathan
author_facet Spiers, Helen
Hannon, Eilis
Schalkwyk, Leonard C.
Bray, Nicholas J.
Mill, Jonathan
author_sort Spiers, Helen
collection PubMed
description BACKGROUND: Epigenetic processes play a key role in orchestrating transcriptional regulation during the development of the human central nervous system. We previously described dynamic changes in DNA methylation (5mC) occurring during human fetal brain development, but other epigenetic processes operating during this period have not been extensively explored. Of particular interest is DNA hydroxymethylation (5hmC), a modification that is enriched in the human brain and hypothesized to play an important role in neuronal function, learning and memory. In this study, we quantify 5hmC across the genome of 71 human fetal brain samples spanning 23 to 184 days post-conception. RESULTS: We identify widespread changes in 5hmC occurring during human brain development, notable sex-differences in 5hmC in the fetal brain, and interactions between 5mC and 5hmC at specific sites. Finally, we identify loci where 5hmC in the fetal brain is associated with genetic variation. CONCLUSIONS: This study represents the first systematic analysis of dynamic changes in 5hmC across human neurodevelopment and highlights the potential importance of this modification in the human brain. A searchable database of our fetal brain 5hmC data is available as a resource to the research community at http://www.epigenomicslab.com/online-data-resources. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article doi:(10.1186/s12864-017-4091-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-56041372017-09-21 5-hydroxymethylcytosine is highly dynamic across human fetal brain development Spiers, Helen Hannon, Eilis Schalkwyk, Leonard C. Bray, Nicholas J. Mill, Jonathan BMC Genomics Research Article BACKGROUND: Epigenetic processes play a key role in orchestrating transcriptional regulation during the development of the human central nervous system. We previously described dynamic changes in DNA methylation (5mC) occurring during human fetal brain development, but other epigenetic processes operating during this period have not been extensively explored. Of particular interest is DNA hydroxymethylation (5hmC), a modification that is enriched in the human brain and hypothesized to play an important role in neuronal function, learning and memory. In this study, we quantify 5hmC across the genome of 71 human fetal brain samples spanning 23 to 184 days post-conception. RESULTS: We identify widespread changes in 5hmC occurring during human brain development, notable sex-differences in 5hmC in the fetal brain, and interactions between 5mC and 5hmC at specific sites. Finally, we identify loci where 5hmC in the fetal brain is associated with genetic variation. CONCLUSIONS: This study represents the first systematic analysis of dynamic changes in 5hmC across human neurodevelopment and highlights the potential importance of this modification in the human brain. A searchable database of our fetal brain 5hmC data is available as a resource to the research community at http://www.epigenomicslab.com/online-data-resources. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article doi:(10.1186/s12864-017-4091-x) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-18 /pmc/articles/PMC5604137/ /pubmed/28923016 http://dx.doi.org/10.1186/s12864-017-4091-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Spiers, Helen
Hannon, Eilis
Schalkwyk, Leonard C.
Bray, Nicholas J.
Mill, Jonathan
5-hydroxymethylcytosine is highly dynamic across human fetal brain development
title 5-hydroxymethylcytosine is highly dynamic across human fetal brain development
title_full 5-hydroxymethylcytosine is highly dynamic across human fetal brain development
title_fullStr 5-hydroxymethylcytosine is highly dynamic across human fetal brain development
title_full_unstemmed 5-hydroxymethylcytosine is highly dynamic across human fetal brain development
title_short 5-hydroxymethylcytosine is highly dynamic across human fetal brain development
title_sort 5-hydroxymethylcytosine is highly dynamic across human fetal brain development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604137/
https://www.ncbi.nlm.nih.gov/pubmed/28923016
http://dx.doi.org/10.1186/s12864-017-4091-x
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