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Mendelian inheritance of trimodal CpG methylation sites suggests distal cis-acting genetic effects

BACKGROUND: Environmentally influenced phenotypes, such as obesity and insulin resistance, can be transmitted over multiple generations. Epigenetic modifications, such as methylation of DNA cytosine-guanine (CpG) pairs, may be carriers of inherited information. At the population level, the methylati...

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Autores principales: Zaghlool, Shaza B., Al-Shafai, Mashael, Al Muftah, Wadha A., Kumar, Pankaj, Gieger, Christian, Waldenberger, Melanie, Falchi, Mario, Suhre, Karsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120560/
https://www.ncbi.nlm.nih.gov/pubmed/27895808
http://dx.doi.org/10.1186/s13148-016-0295-1
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author Zaghlool, Shaza B.
Al-Shafai, Mashael
Al Muftah, Wadha A.
Kumar, Pankaj
Gieger, Christian
Waldenberger, Melanie
Falchi, Mario
Suhre, Karsten
author_facet Zaghlool, Shaza B.
Al-Shafai, Mashael
Al Muftah, Wadha A.
Kumar, Pankaj
Gieger, Christian
Waldenberger, Melanie
Falchi, Mario
Suhre, Karsten
author_sort Zaghlool, Shaza B.
collection PubMed
description BACKGROUND: Environmentally influenced phenotypes, such as obesity and insulin resistance, can be transmitted over multiple generations. Epigenetic modifications, such as methylation of DNA cytosine-guanine (CpG) pairs, may be carriers of inherited information. At the population level, the methylation state of such “heritable” CpG sites is expected to follow a trimodal distribution, and their mode of inheritance should be Mendelian. METHODS: Using the Illumina Infinium 450 K DNA methylation array, we determined DNA CpG-methylation in blood cells from a family cohort 123 individuals of Arab ethnicity, including 18 elementary father-mother-child trios, we asked whether Mendelian inheritance of CpG methylation is observed, and most importantly, whether it is independent of any genetic signals. Using 40× whole genome sequencing, we therefore excluded all CpG sites with possibly confounding genetic variants (SNP) within the binding regions of the Illumina probes. RESULTS: We identified a total of 955 CpG sites that displayed a trimodal distribution and confirmed trimodality in a study of 1805 unrelated Caucasians. Of 955 CpG sites, 99.9% observed a strict Mendelian pattern of inheritance and had no SNP within +/−110 nucleotides of the CpG site by design. However, in 97% of these cases a distal cis-acting SNP within a +/−1 Mbp window was found that explained the observed CpG distribution, excluding the hypothesis of epigenetic inheritance for these clear-cut trimodal sites. Using power analysis, we showed that in 46% of all cases, the closest CpG-associated SNP was located more than 1000 bp from the CpG site. CONCLUSIONS: Our findings suggest that CpG methylation is maintained over larger genomic distances. Furthermore, nearly half of the SNPs associated with these trimodal sites were also associated with the expression of nearby genes (P = 4.08 × 10(−6)), implying a regulatory effect of these trimodal CpG sites. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13148-016-0295-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-51205602016-11-28 Mendelian inheritance of trimodal CpG methylation sites suggests distal cis-acting genetic effects Zaghlool, Shaza B. Al-Shafai, Mashael Al Muftah, Wadha A. Kumar, Pankaj Gieger, Christian Waldenberger, Melanie Falchi, Mario Suhre, Karsten Clin Epigenetics Research BACKGROUND: Environmentally influenced phenotypes, such as obesity and insulin resistance, can be transmitted over multiple generations. Epigenetic modifications, such as methylation of DNA cytosine-guanine (CpG) pairs, may be carriers of inherited information. At the population level, the methylation state of such “heritable” CpG sites is expected to follow a trimodal distribution, and their mode of inheritance should be Mendelian. METHODS: Using the Illumina Infinium 450 K DNA methylation array, we determined DNA CpG-methylation in blood cells from a family cohort 123 individuals of Arab ethnicity, including 18 elementary father-mother-child trios, we asked whether Mendelian inheritance of CpG methylation is observed, and most importantly, whether it is independent of any genetic signals. Using 40× whole genome sequencing, we therefore excluded all CpG sites with possibly confounding genetic variants (SNP) within the binding regions of the Illumina probes. RESULTS: We identified a total of 955 CpG sites that displayed a trimodal distribution and confirmed trimodality in a study of 1805 unrelated Caucasians. Of 955 CpG sites, 99.9% observed a strict Mendelian pattern of inheritance and had no SNP within +/−110 nucleotides of the CpG site by design. However, in 97% of these cases a distal cis-acting SNP within a +/−1 Mbp window was found that explained the observed CpG distribution, excluding the hypothesis of epigenetic inheritance for these clear-cut trimodal sites. Using power analysis, we showed that in 46% of all cases, the closest CpG-associated SNP was located more than 1000 bp from the CpG site. CONCLUSIONS: Our findings suggest that CpG methylation is maintained over larger genomic distances. Furthermore, nearly half of the SNPs associated with these trimodal sites were also associated with the expression of nearby genes (P = 4.08 × 10(−6)), implying a regulatory effect of these trimodal CpG sites. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13148-016-0295-1) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-22 /pmc/articles/PMC5120560/ /pubmed/27895808 http://dx.doi.org/10.1186/s13148-016-0295-1 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zaghlool, Shaza B.
Al-Shafai, Mashael
Al Muftah, Wadha A.
Kumar, Pankaj
Gieger, Christian
Waldenberger, Melanie
Falchi, Mario
Suhre, Karsten
Mendelian inheritance of trimodal CpG methylation sites suggests distal cis-acting genetic effects
title Mendelian inheritance of trimodal CpG methylation sites suggests distal cis-acting genetic effects
title_full Mendelian inheritance of trimodal CpG methylation sites suggests distal cis-acting genetic effects
title_fullStr Mendelian inheritance of trimodal CpG methylation sites suggests distal cis-acting genetic effects
title_full_unstemmed Mendelian inheritance of trimodal CpG methylation sites suggests distal cis-acting genetic effects
title_short Mendelian inheritance of trimodal CpG methylation sites suggests distal cis-acting genetic effects
title_sort mendelian inheritance of trimodal cpg methylation sites suggests distal cis-acting genetic effects
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120560/
https://www.ncbi.nlm.nih.gov/pubmed/27895808
http://dx.doi.org/10.1186/s13148-016-0295-1
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