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GWAS loci associated with Chagas cardiomyopathy influences DNA methylation levels

A recent genome-wide association study (GWAS) identified a locus in chromosome 11 associated with the chronic cardiac form of Chagas disease. Here we aimed to elucidate the potential functional mechanism underlying this genetic association by analyzing the correlation among single nucleotide polymor...

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Autores principales: Casares-Marfil, Desiré, Kerick, Martin, Andrés-León, Eduardo, Bosch-Nicolau, Pau, Molina, Israel, Martin, Javier, Acosta-Herrera, Marialbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580254/
https://www.ncbi.nlm.nih.gov/pubmed/34714828
http://dx.doi.org/10.1371/journal.pntd.0009874
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author Casares-Marfil, Desiré
Kerick, Martin
Andrés-León, Eduardo
Bosch-Nicolau, Pau
Molina, Israel
Martin, Javier
Acosta-Herrera, Marialbert
author_facet Casares-Marfil, Desiré
Kerick, Martin
Andrés-León, Eduardo
Bosch-Nicolau, Pau
Molina, Israel
Martin, Javier
Acosta-Herrera, Marialbert
author_sort Casares-Marfil, Desiré
collection PubMed
description A recent genome-wide association study (GWAS) identified a locus in chromosome 11 associated with the chronic cardiac form of Chagas disease. Here we aimed to elucidate the potential functional mechanism underlying this genetic association by analyzing the correlation among single nucleotide polymorphisms (SNPs) and DNA methylation (DNAm) levels as cis methylation quantitative trait loci (cis-mQTL) within this region. A total of 2,611 SNPs were tested against 2,647 DNAm sites, in a subset of 37 chronic Chagas cardiomyopathy patients and 20 asymptomatic individuals from the GWAS. We identified 6,958 significant cis-mQTLs (False Discovery Rate [FDR]<0.05) at 1 Mb each side of the GWAS leading variant, where six of them potentially modulate the expression of the SAC3D1 gene, the reported gene in the previous GWAS. In addition, a total of 268 cis-mQTLs showed differential methylation between chronic Chagas cardiomyopathy patients and asymptomatic individuals. The most significant cis-mQTLs mapped in the gene bodies of POLA2 (FDR = 1.04x10(-11)), PLAAT3 (FDR = 7.22x10(-03)), and CCDC88B (FDR = 1.89x10(-02)) that have been associated with cardiovascular and hematological traits in previous studies. One of the most relevant interactions correlated with hypermethylation of CCDC88B. This gene is involved in the inflammatory response, and its methylation and expression levels have been previously reported in Chagas cardiomyopathy. Our findings support the functional relevance of the previously associated genomic region, highlighting the regulation of novel genes that could play a role in the chronic cardiac form of the disease.
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spelling pubmed-85802542021-11-11 GWAS loci associated with Chagas cardiomyopathy influences DNA methylation levels Casares-Marfil, Desiré Kerick, Martin Andrés-León, Eduardo Bosch-Nicolau, Pau Molina, Israel Martin, Javier Acosta-Herrera, Marialbert PLoS Negl Trop Dis Research Article A recent genome-wide association study (GWAS) identified a locus in chromosome 11 associated with the chronic cardiac form of Chagas disease. Here we aimed to elucidate the potential functional mechanism underlying this genetic association by analyzing the correlation among single nucleotide polymorphisms (SNPs) and DNA methylation (DNAm) levels as cis methylation quantitative trait loci (cis-mQTL) within this region. A total of 2,611 SNPs were tested against 2,647 DNAm sites, in a subset of 37 chronic Chagas cardiomyopathy patients and 20 asymptomatic individuals from the GWAS. We identified 6,958 significant cis-mQTLs (False Discovery Rate [FDR]<0.05) at 1 Mb each side of the GWAS leading variant, where six of them potentially modulate the expression of the SAC3D1 gene, the reported gene in the previous GWAS. In addition, a total of 268 cis-mQTLs showed differential methylation between chronic Chagas cardiomyopathy patients and asymptomatic individuals. The most significant cis-mQTLs mapped in the gene bodies of POLA2 (FDR = 1.04x10(-11)), PLAAT3 (FDR = 7.22x10(-03)), and CCDC88B (FDR = 1.89x10(-02)) that have been associated with cardiovascular and hematological traits in previous studies. One of the most relevant interactions correlated with hypermethylation of CCDC88B. This gene is involved in the inflammatory response, and its methylation and expression levels have been previously reported in Chagas cardiomyopathy. Our findings support the functional relevance of the previously associated genomic region, highlighting the regulation of novel genes that could play a role in the chronic cardiac form of the disease. Public Library of Science 2021-10-29 /pmc/articles/PMC8580254/ /pubmed/34714828 http://dx.doi.org/10.1371/journal.pntd.0009874 Text en © 2021 Casares-Marfil et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Casares-Marfil, Desiré
Kerick, Martin
Andrés-León, Eduardo
Bosch-Nicolau, Pau
Molina, Israel
Martin, Javier
Acosta-Herrera, Marialbert
GWAS loci associated with Chagas cardiomyopathy influences DNA methylation levels
title GWAS loci associated with Chagas cardiomyopathy influences DNA methylation levels
title_full GWAS loci associated with Chagas cardiomyopathy influences DNA methylation levels
title_fullStr GWAS loci associated with Chagas cardiomyopathy influences DNA methylation levels
title_full_unstemmed GWAS loci associated with Chagas cardiomyopathy influences DNA methylation levels
title_short GWAS loci associated with Chagas cardiomyopathy influences DNA methylation levels
title_sort gwas loci associated with chagas cardiomyopathy influences dna methylation levels
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580254/
https://www.ncbi.nlm.nih.gov/pubmed/34714828
http://dx.doi.org/10.1371/journal.pntd.0009874
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