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DNA hypomethylation during MSC chondrogenesis occurs predominantly at enhancer regions

Regulation of transcription occurs in a cell type specific manner orchestrated by epigenetic mechanisms including DNA methylation. Methylation changes may also play a key role in lineage specification during stem cell differentiation. To further our understanding of epigenetic regulation in chondroc...

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Autores principales: Barter, Matt J., Bui, Catherine, Cheung, Kathleen, Falk, Julia, Gómez, Rodolfo, Skelton, Andrew J., Elliott, Hannah R., Reynard, Louise N., Young, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981252/
https://www.ncbi.nlm.nih.gov/pubmed/31980739
http://dx.doi.org/10.1038/s41598-020-58093-5
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author Barter, Matt J.
Bui, Catherine
Cheung, Kathleen
Falk, Julia
Gómez, Rodolfo
Skelton, Andrew J.
Elliott, Hannah R.
Reynard, Louise N.
Young, David A.
author_facet Barter, Matt J.
Bui, Catherine
Cheung, Kathleen
Falk, Julia
Gómez, Rodolfo
Skelton, Andrew J.
Elliott, Hannah R.
Reynard, Louise N.
Young, David A.
author_sort Barter, Matt J.
collection PubMed
description Regulation of transcription occurs in a cell type specific manner orchestrated by epigenetic mechanisms including DNA methylation. Methylation changes may also play a key role in lineage specification during stem cell differentiation. To further our understanding of epigenetic regulation in chondrocytes we characterised the DNA methylation changes during chondrogenesis of mesenchymal stem cells (MSCs) by Infinium 450 K methylation array. Significant DNA hypomethylation was identified during chondrogenic differentiation including changes at many key cartilage gene loci. Integration with chondrogenesis gene expression data revealed an enrichment of significant CpGs in upregulated genes, while characterisation of significant CpG loci indicated their predominant localisation to enhancer regions. Comparison with methylation profiles of other tissues, including healthy and diseased adult cartilage, identified chondrocyte-specific regions of hypomethylation and the overlap with differentially methylated CpGs in osteoarthritis. Taken together we have associated DNA methylation levels with the chondrocyte phenotype. The consequences of which has potential to improve cartilage generation for tissue engineering purposes and also to provide context for observed methylation changes in cartilage diseases such as osteoarthritis.
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spelling pubmed-69812522020-01-30 DNA hypomethylation during MSC chondrogenesis occurs predominantly at enhancer regions Barter, Matt J. Bui, Catherine Cheung, Kathleen Falk, Julia Gómez, Rodolfo Skelton, Andrew J. Elliott, Hannah R. Reynard, Louise N. Young, David A. Sci Rep Article Regulation of transcription occurs in a cell type specific manner orchestrated by epigenetic mechanisms including DNA methylation. Methylation changes may also play a key role in lineage specification during stem cell differentiation. To further our understanding of epigenetic regulation in chondrocytes we characterised the DNA methylation changes during chondrogenesis of mesenchymal stem cells (MSCs) by Infinium 450 K methylation array. Significant DNA hypomethylation was identified during chondrogenic differentiation including changes at many key cartilage gene loci. Integration with chondrogenesis gene expression data revealed an enrichment of significant CpGs in upregulated genes, while characterisation of significant CpG loci indicated their predominant localisation to enhancer regions. Comparison with methylation profiles of other tissues, including healthy and diseased adult cartilage, identified chondrocyte-specific regions of hypomethylation and the overlap with differentially methylated CpGs in osteoarthritis. Taken together we have associated DNA methylation levels with the chondrocyte phenotype. The consequences of which has potential to improve cartilage generation for tissue engineering purposes and also to provide context for observed methylation changes in cartilage diseases such as osteoarthritis. Nature Publishing Group UK 2020-01-24 /pmc/articles/PMC6981252/ /pubmed/31980739 http://dx.doi.org/10.1038/s41598-020-58093-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Barter, Matt J.
Bui, Catherine
Cheung, Kathleen
Falk, Julia
Gómez, Rodolfo
Skelton, Andrew J.
Elliott, Hannah R.
Reynard, Louise N.
Young, David A.
DNA hypomethylation during MSC chondrogenesis occurs predominantly at enhancer regions
title DNA hypomethylation during MSC chondrogenesis occurs predominantly at enhancer regions
title_full DNA hypomethylation during MSC chondrogenesis occurs predominantly at enhancer regions
title_fullStr DNA hypomethylation during MSC chondrogenesis occurs predominantly at enhancer regions
title_full_unstemmed DNA hypomethylation during MSC chondrogenesis occurs predominantly at enhancer regions
title_short DNA hypomethylation during MSC chondrogenesis occurs predominantly at enhancer regions
title_sort dna hypomethylation during msc chondrogenesis occurs predominantly at enhancer regions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981252/
https://www.ncbi.nlm.nih.gov/pubmed/31980739
http://dx.doi.org/10.1038/s41598-020-58093-5
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