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Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation
Global loss of DNA methylation and CpG island (CGI) hypermethylation are key epigenomic aberrations in cancer. Global loss manifests itself in partially methylated domains (PMDs) which extend up to megabases. However, the distribution of PMDs within and between tumor types, and their effects on key...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465362/ https://www.ncbi.nlm.nih.gov/pubmed/30988298 http://dx.doi.org/10.1038/s41467-019-09828-0 |
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author | Brinkman, Arie B. Nik-Zainal, Serena Simmer, Femke Rodríguez-González, F. Germán Smid, Marcel Alexandrov, Ludmil B. Butler, Adam Martin, Sancha Davies, Helen Glodzik, Dominik Zou, Xueqing Ramakrishna, Manasa Staaf, Johan Ringnér, Markus Sieuwerts, Anieta Ferrari, Anthony Morganella, Sandro Fleischer, Thomas Kristensen, Vessela Gut, Marta van de Vijver, Marc J. Børresen-Dale, Anne-Lise Richardson, Andrea L. Thomas, Gilles Gut, Ivo G. Martens, John W. M. Foekens, John A. Stratton, Michael R. Stunnenberg, Hendrik G. |
author_facet | Brinkman, Arie B. Nik-Zainal, Serena Simmer, Femke Rodríguez-González, F. Germán Smid, Marcel Alexandrov, Ludmil B. Butler, Adam Martin, Sancha Davies, Helen Glodzik, Dominik Zou, Xueqing Ramakrishna, Manasa Staaf, Johan Ringnér, Markus Sieuwerts, Anieta Ferrari, Anthony Morganella, Sandro Fleischer, Thomas Kristensen, Vessela Gut, Marta van de Vijver, Marc J. Børresen-Dale, Anne-Lise Richardson, Andrea L. Thomas, Gilles Gut, Ivo G. Martens, John W. M. Foekens, John A. Stratton, Michael R. Stunnenberg, Hendrik G. |
author_sort | Brinkman, Arie B. |
collection | PubMed |
description | Global loss of DNA methylation and CpG island (CGI) hypermethylation are key epigenomic aberrations in cancer. Global loss manifests itself in partially methylated domains (PMDs) which extend up to megabases. However, the distribution of PMDs within and between tumor types, and their effects on key functional genomic elements including CGIs are poorly defined. We comprehensively show that loss of methylation in PMDs occurs in a large fraction of the genome and represents the prime source of DNA methylation variation. PMDs are hypervariable in methylation level, size and distribution, and display elevated mutation rates. They impose intermediate DNA methylation levels incognizant of functional genomic elements including CGIs, underpinning a CGI methylator phenotype (CIMP). Repression effects on tumor suppressor genes are negligible as they are generally excluded from PMDs. The genomic distribution of PMDs reports tissue-of-origin and may represent tissue-specific silent regions which tolerate instability at the epigenetic, transcriptomic and genetic level. |
format | Online Article Text |
id | pubmed-6465362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64653622019-04-17 Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation Brinkman, Arie B. Nik-Zainal, Serena Simmer, Femke Rodríguez-González, F. Germán Smid, Marcel Alexandrov, Ludmil B. Butler, Adam Martin, Sancha Davies, Helen Glodzik, Dominik Zou, Xueqing Ramakrishna, Manasa Staaf, Johan Ringnér, Markus Sieuwerts, Anieta Ferrari, Anthony Morganella, Sandro Fleischer, Thomas Kristensen, Vessela Gut, Marta van de Vijver, Marc J. Børresen-Dale, Anne-Lise Richardson, Andrea L. Thomas, Gilles Gut, Ivo G. Martens, John W. M. Foekens, John A. Stratton, Michael R. Stunnenberg, Hendrik G. Nat Commun Article Global loss of DNA methylation and CpG island (CGI) hypermethylation are key epigenomic aberrations in cancer. Global loss manifests itself in partially methylated domains (PMDs) which extend up to megabases. However, the distribution of PMDs within and between tumor types, and their effects on key functional genomic elements including CGIs are poorly defined. We comprehensively show that loss of methylation in PMDs occurs in a large fraction of the genome and represents the prime source of DNA methylation variation. PMDs are hypervariable in methylation level, size and distribution, and display elevated mutation rates. They impose intermediate DNA methylation levels incognizant of functional genomic elements including CGIs, underpinning a CGI methylator phenotype (CIMP). Repression effects on tumor suppressor genes are negligible as they are generally excluded from PMDs. The genomic distribution of PMDs reports tissue-of-origin and may represent tissue-specific silent regions which tolerate instability at the epigenetic, transcriptomic and genetic level. Nature Publishing Group UK 2019-04-15 /pmc/articles/PMC6465362/ /pubmed/30988298 http://dx.doi.org/10.1038/s41467-019-09828-0 Text en © The Author(s) 2019 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 Brinkman, Arie B. Nik-Zainal, Serena Simmer, Femke Rodríguez-González, F. Germán Smid, Marcel Alexandrov, Ludmil B. Butler, Adam Martin, Sancha Davies, Helen Glodzik, Dominik Zou, Xueqing Ramakrishna, Manasa Staaf, Johan Ringnér, Markus Sieuwerts, Anieta Ferrari, Anthony Morganella, Sandro Fleischer, Thomas Kristensen, Vessela Gut, Marta van de Vijver, Marc J. Børresen-Dale, Anne-Lise Richardson, Andrea L. Thomas, Gilles Gut, Ivo G. Martens, John W. M. Foekens, John A. Stratton, Michael R. Stunnenberg, Hendrik G. Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation |
title | Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation |
title_full | Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation |
title_fullStr | Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation |
title_full_unstemmed | Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation |
title_short | Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation |
title_sort | partially methylated domains are hypervariable in breast cancer and fuel widespread cpg island hypermethylation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465362/ https://www.ncbi.nlm.nih.gov/pubmed/30988298 http://dx.doi.org/10.1038/s41467-019-09828-0 |
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