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Population-specificity of human DNA methylation
BACKGROUND: Ethnic differences in human DNA methylation have been shown for a number of CpG sites, but the genome-wide patterns and extent of these differences are largely unknown. In addition, whether the genetic control of polymorphic DNA methylation is population-specific has not been investigate...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334571/ https://www.ncbi.nlm.nih.gov/pubmed/22322129 http://dx.doi.org/10.1186/gb-2012-13-2-r8 |
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author | Fraser, Hunter B Lam, Lucia L Neumann, Sarah M Kobor, Michael S |
author_facet | Fraser, Hunter B Lam, Lucia L Neumann, Sarah M Kobor, Michael S |
author_sort | Fraser, Hunter B |
collection | PubMed |
description | BACKGROUND: Ethnic differences in human DNA methylation have been shown for a number of CpG sites, but the genome-wide patterns and extent of these differences are largely unknown. In addition, whether the genetic control of polymorphic DNA methylation is population-specific has not been investigated. RESULTS: Here we measure DNA methylation near the transcription start sites of over 14, 000 genes in 180 cell lines derived from one African and one European population. We find population-specific patterns of DNA methylation at over a third of all genes. Furthermore, although the methylation at over a thousand CpG sites is heritable, these heritabilities also differ between populations, suggesting extensive divergence in the genetic control of DNA methylation. In support of this, genetic mapping of DNA methylation reveals that most of the population specificity can be explained by divergence in allele frequencies between populations, and that there is little overlap in genetic associations between populations. These population-specific genetic associations are supported by the patterns of DNA methylation in several hundred brain samples, suggesting that they hold in vivo and across tissues. CONCLUSIONS: These results suggest that DNA methylation is highly divergent between populations, and that this divergence may be due in large part to a combination of differences in allele frequencies and complex epistasis or gene × environment interactions. |
format | Online Article Text |
id | pubmed-3334571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33345712012-04-25 Population-specificity of human DNA methylation Fraser, Hunter B Lam, Lucia L Neumann, Sarah M Kobor, Michael S Genome Biol Research BACKGROUND: Ethnic differences in human DNA methylation have been shown for a number of CpG sites, but the genome-wide patterns and extent of these differences are largely unknown. In addition, whether the genetic control of polymorphic DNA methylation is population-specific has not been investigated. RESULTS: Here we measure DNA methylation near the transcription start sites of over 14, 000 genes in 180 cell lines derived from one African and one European population. We find population-specific patterns of DNA methylation at over a third of all genes. Furthermore, although the methylation at over a thousand CpG sites is heritable, these heritabilities also differ between populations, suggesting extensive divergence in the genetic control of DNA methylation. In support of this, genetic mapping of DNA methylation reveals that most of the population specificity can be explained by divergence in allele frequencies between populations, and that there is little overlap in genetic associations between populations. These population-specific genetic associations are supported by the patterns of DNA methylation in several hundred brain samples, suggesting that they hold in vivo and across tissues. CONCLUSIONS: These results suggest that DNA methylation is highly divergent between populations, and that this divergence may be due in large part to a combination of differences in allele frequencies and complex epistasis or gene × environment interactions. BioMed Central 2012 2012-02-09 /pmc/articles/PMC3334571/ /pubmed/22322129 http://dx.doi.org/10.1186/gb-2012-13-2-r8 Text en Copyright ©2012 Fraser et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Fraser, Hunter B Lam, Lucia L Neumann, Sarah M Kobor, Michael S Population-specificity of human DNA methylation |
title | Population-specificity of human DNA methylation |
title_full | Population-specificity of human DNA methylation |
title_fullStr | Population-specificity of human DNA methylation |
title_full_unstemmed | Population-specificity of human DNA methylation |
title_short | Population-specificity of human DNA methylation |
title_sort | population-specificity of human dna methylation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334571/ https://www.ncbi.nlm.nih.gov/pubmed/22322129 http://dx.doi.org/10.1186/gb-2012-13-2-r8 |
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