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Allele-Specific Methylation Occurs at Genetic Variants Associated with Complex Disease

We hypothesize that the phenomenon of allele-specific methylation (ASM) may underlie the phenotypic effects of multiple variants identified by Genome-Wide Association studies (GWAS). We evaluate ASM in a human population and document its genome-wide patterns in an initial screen at up to 380,678 sit...

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Autores principales: Hutchinson, John N., Raj, Towfique, Fagerness, Jes, Stahl, Eli, Viloria, Fernando T., Gimelbrant, Alexander, Seddon, Johanna, Daly, Mark, Chess, Andrew, Plenge, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049588/
https://www.ncbi.nlm.nih.gov/pubmed/24911414
http://dx.doi.org/10.1371/journal.pone.0098464
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author Hutchinson, John N.
Raj, Towfique
Fagerness, Jes
Stahl, Eli
Viloria, Fernando T.
Gimelbrant, Alexander
Seddon, Johanna
Daly, Mark
Chess, Andrew
Plenge, Robert
author_facet Hutchinson, John N.
Raj, Towfique
Fagerness, Jes
Stahl, Eli
Viloria, Fernando T.
Gimelbrant, Alexander
Seddon, Johanna
Daly, Mark
Chess, Andrew
Plenge, Robert
author_sort Hutchinson, John N.
collection PubMed
description We hypothesize that the phenomenon of allele-specific methylation (ASM) may underlie the phenotypic effects of multiple variants identified by Genome-Wide Association studies (GWAS). We evaluate ASM in a human population and document its genome-wide patterns in an initial screen at up to 380,678 sites within the genome, or up to 5% of the total genomic CpGs. We show that while substantial inter-individual variation exists, 5% of assessed sites show evidence of ASM in at least six samples; the majority of these events (81%) are under genetic influence. Many of these cis-regulated ASM variants are also eQTLs in peripheral blood mononuclear cells and monocytes and/or in high linkage-disequilibrium with variants linked to complex disease. Finally, focusing on autoimmune phenotypes, we extend this initial screen to confirm the association of cis-regulated ASM with multiple complex disease-associated variants in an independent population using next-generation bisulfite sequencing. These four variants are implicated in complex phenotypes such as ulcerative colitis and AIDS progression disease (rs10491434), Celiac disease (rs2762051), Crohn's disease, IgA nephropathy and early-onset inflammatory bowel disease (rs713875) and height (rs6569648). Our results suggest cis-regulated ASM may provide a mechanistic link between the non-coding genetic changes and phenotypic variation observed in these diseases and further suggests a route to integrating DNA methylation status with GWAS results.
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spelling pubmed-40495882014-06-18 Allele-Specific Methylation Occurs at Genetic Variants Associated with Complex Disease Hutchinson, John N. Raj, Towfique Fagerness, Jes Stahl, Eli Viloria, Fernando T. Gimelbrant, Alexander Seddon, Johanna Daly, Mark Chess, Andrew Plenge, Robert PLoS One Research Article We hypothesize that the phenomenon of allele-specific methylation (ASM) may underlie the phenotypic effects of multiple variants identified by Genome-Wide Association studies (GWAS). We evaluate ASM in a human population and document its genome-wide patterns in an initial screen at up to 380,678 sites within the genome, or up to 5% of the total genomic CpGs. We show that while substantial inter-individual variation exists, 5% of assessed sites show evidence of ASM in at least six samples; the majority of these events (81%) are under genetic influence. Many of these cis-regulated ASM variants are also eQTLs in peripheral blood mononuclear cells and monocytes and/or in high linkage-disequilibrium with variants linked to complex disease. Finally, focusing on autoimmune phenotypes, we extend this initial screen to confirm the association of cis-regulated ASM with multiple complex disease-associated variants in an independent population using next-generation bisulfite sequencing. These four variants are implicated in complex phenotypes such as ulcerative colitis and AIDS progression disease (rs10491434), Celiac disease (rs2762051), Crohn's disease, IgA nephropathy and early-onset inflammatory bowel disease (rs713875) and height (rs6569648). Our results suggest cis-regulated ASM may provide a mechanistic link between the non-coding genetic changes and phenotypic variation observed in these diseases and further suggests a route to integrating DNA methylation status with GWAS results. Public Library of Science 2014-06-09 /pmc/articles/PMC4049588/ /pubmed/24911414 http://dx.doi.org/10.1371/journal.pone.0098464 Text en © 2014 Hutchinson et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hutchinson, John N.
Raj, Towfique
Fagerness, Jes
Stahl, Eli
Viloria, Fernando T.
Gimelbrant, Alexander
Seddon, Johanna
Daly, Mark
Chess, Andrew
Plenge, Robert
Allele-Specific Methylation Occurs at Genetic Variants Associated with Complex Disease
title Allele-Specific Methylation Occurs at Genetic Variants Associated with Complex Disease
title_full Allele-Specific Methylation Occurs at Genetic Variants Associated with Complex Disease
title_fullStr Allele-Specific Methylation Occurs at Genetic Variants Associated with Complex Disease
title_full_unstemmed Allele-Specific Methylation Occurs at Genetic Variants Associated with Complex Disease
title_short Allele-Specific Methylation Occurs at Genetic Variants Associated with Complex Disease
title_sort allele-specific methylation occurs at genetic variants associated with complex disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049588/
https://www.ncbi.nlm.nih.gov/pubmed/24911414
http://dx.doi.org/10.1371/journal.pone.0098464
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