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Discovering high-resolution patterns of differential DNA methylation that correlate with gene expression changes
Methylation of the CpG-rich region (CpG island) overlapping a gene’s promoter is a generally accepted mechanism for silencing expression. While recent technological advances have enabled measurement of DNA methylation and expression changes genome-wide, only modest correlations between differential...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3737560/ https://www.ncbi.nlm.nih.gov/pubmed/23748561 http://dx.doi.org/10.1093/nar/gkt482 |
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author | VanderKraats, Nathan D. Hiken, Jeffrey F. Decker, Keith F. Edwards, John R. |
author_facet | VanderKraats, Nathan D. Hiken, Jeffrey F. Decker, Keith F. Edwards, John R. |
author_sort | VanderKraats, Nathan D. |
collection | PubMed |
description | Methylation of the CpG-rich region (CpG island) overlapping a gene’s promoter is a generally accepted mechanism for silencing expression. While recent technological advances have enabled measurement of DNA methylation and expression changes genome-wide, only modest correlations between differential methylation at gene promoters and expression have been found. We hypothesize that stronger associations are not observed because existing analysis methods oversimplify their representation of the data and do not capture the diversity of existing methylation patterns. Recently, other patterns such as CpG island shore methylation and long partially hypomethylated domains have also been linked with gene silencing. Here, we detail a new approach for discovering differential methylation patterns associated with expression change using genome-wide high-resolution methylation data: we represent differential methylation as an interpolated curve, or signature, and then identify groups of genes with similarly shaped signatures and corresponding expression changes. Our technique uncovers a diverse set of patterns that are conserved across embryonic stem cell and cancer data sets. Overall, we find strong associations between these methylation patterns and expression. We further show that an extension of our method also outperforms other approaches by generating a longer list of genes with higher quality associations between differential methylation and expression. |
format | Online Article Text |
id | pubmed-3737560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37375602013-08-08 Discovering high-resolution patterns of differential DNA methylation that correlate with gene expression changes VanderKraats, Nathan D. Hiken, Jeffrey F. Decker, Keith F. Edwards, John R. Nucleic Acids Res Computational Biology Methylation of the CpG-rich region (CpG island) overlapping a gene’s promoter is a generally accepted mechanism for silencing expression. While recent technological advances have enabled measurement of DNA methylation and expression changes genome-wide, only modest correlations between differential methylation at gene promoters and expression have been found. We hypothesize that stronger associations are not observed because existing analysis methods oversimplify their representation of the data and do not capture the diversity of existing methylation patterns. Recently, other patterns such as CpG island shore methylation and long partially hypomethylated domains have also been linked with gene silencing. Here, we detail a new approach for discovering differential methylation patterns associated with expression change using genome-wide high-resolution methylation data: we represent differential methylation as an interpolated curve, or signature, and then identify groups of genes with similarly shaped signatures and corresponding expression changes. Our technique uncovers a diverse set of patterns that are conserved across embryonic stem cell and cancer data sets. Overall, we find strong associations between these methylation patterns and expression. We further show that an extension of our method also outperforms other approaches by generating a longer list of genes with higher quality associations between differential methylation and expression. Oxford University Press 2013-08 2013-06-07 /pmc/articles/PMC3737560/ /pubmed/23748561 http://dx.doi.org/10.1093/nar/gkt482 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Computational Biology VanderKraats, Nathan D. Hiken, Jeffrey F. Decker, Keith F. Edwards, John R. Discovering high-resolution patterns of differential DNA methylation that correlate with gene expression changes |
title | Discovering high-resolution patterns of differential DNA methylation that correlate with gene expression changes |
title_full | Discovering high-resolution patterns of differential DNA methylation that correlate with gene expression changes |
title_fullStr | Discovering high-resolution patterns of differential DNA methylation that correlate with gene expression changes |
title_full_unstemmed | Discovering high-resolution patterns of differential DNA methylation that correlate with gene expression changes |
title_short | Discovering high-resolution patterns of differential DNA methylation that correlate with gene expression changes |
title_sort | discovering high-resolution patterns of differential dna methylation that correlate with gene expression changes |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3737560/ https://www.ncbi.nlm.nih.gov/pubmed/23748561 http://dx.doi.org/10.1093/nar/gkt482 |
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