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Uncovering the DNA methylation landscape in key regulatory regions within the FADS cluster

Genetic variants near and within the fatty acid desaturase (FADS) cluster are associated with polyunsaturated fatty acid (PUFA) biosynthesis, levels of several disease biomarkers and risk of human disease. However, determining the functional mechanisms by which these genetic variants impact PUFA lev...

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Autores principales: Rahbar, Elaheh, Ainsworth, Hannah C., Howard, Timothy D., Hawkins, Gregory A., Ruczinski, Ingo, Mathias, Rasika, Seeds, Michael C., Sergeant, Susan, Hixson, James E., Herrington, David M., Langefeld, Carl D., Chilton, Floyd H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5619705/
https://www.ncbi.nlm.nih.gov/pubmed/28957329
http://dx.doi.org/10.1371/journal.pone.0180903
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author Rahbar, Elaheh
Ainsworth, Hannah C.
Howard, Timothy D.
Hawkins, Gregory A.
Ruczinski, Ingo
Mathias, Rasika
Seeds, Michael C.
Sergeant, Susan
Hixson, James E.
Herrington, David M.
Langefeld, Carl D.
Chilton, Floyd H.
author_facet Rahbar, Elaheh
Ainsworth, Hannah C.
Howard, Timothy D.
Hawkins, Gregory A.
Ruczinski, Ingo
Mathias, Rasika
Seeds, Michael C.
Sergeant, Susan
Hixson, James E.
Herrington, David M.
Langefeld, Carl D.
Chilton, Floyd H.
author_sort Rahbar, Elaheh
collection PubMed
description Genetic variants near and within the fatty acid desaturase (FADS) cluster are associated with polyunsaturated fatty acid (PUFA) biosynthesis, levels of several disease biomarkers and risk of human disease. However, determining the functional mechanisms by which these genetic variants impact PUFA levels remains a challenge. Utilizing an Illumina 450K array, we previously reported strong allele-specific methylation (ASM) associations (p = 2.69×10(−29)) between a single nucleotide polymorphism (SNP) rs174537 and DNA methylation of CpG sites located in the putative enhancer region between FADS1 and FADS2, in human liver tissue. However, this array only featured 20 CpG sites within this 12kb region. To better understand the methylation landscape within this region, we conducted bisulfite sequencing of the region between FADS1 and FADS2. Liver tissues from 50 male subjects (27 European Americans, 23 African Americans) were obtained from the Pathobiological Determinants of Atherosclerosis in Youth (PDAY) study, and used to ascertain the genotype at rs174537 and methylation status across the region of interest. Associations between rs174537 genotype and methylation status of 136 CpG sites were determined. Age-adjusted linear regressions were used to assess ASM associations with rs174537 genotype. The majority of CpG sites (117 out of 136, 86%) exhibited high levels of methylation with the greatest variability observed at three key regulatory regions–the promoter regions for FADS1 and FADS2 and a putative enhancer site between the two genes. Eight CpG sites within the putative enhancer region displayed significant (FDR p <0.05) ASM associations with rs174537. These data support the concept that both genetic and epigenetic factors regulate PUFA biosynthesis, and raise fundamental questions as to how genetic variants such as rs174537 impact DNA methylation in distant regulatory regions, and ultimately the capacity of tissues to synthesize PUFAs.
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spelling pubmed-56197052017-10-17 Uncovering the DNA methylation landscape in key regulatory regions within the FADS cluster Rahbar, Elaheh Ainsworth, Hannah C. Howard, Timothy D. Hawkins, Gregory A. Ruczinski, Ingo Mathias, Rasika Seeds, Michael C. Sergeant, Susan Hixson, James E. Herrington, David M. Langefeld, Carl D. Chilton, Floyd H. PLoS One Research Article Genetic variants near and within the fatty acid desaturase (FADS) cluster are associated with polyunsaturated fatty acid (PUFA) biosynthesis, levels of several disease biomarkers and risk of human disease. However, determining the functional mechanisms by which these genetic variants impact PUFA levels remains a challenge. Utilizing an Illumina 450K array, we previously reported strong allele-specific methylation (ASM) associations (p = 2.69×10(−29)) between a single nucleotide polymorphism (SNP) rs174537 and DNA methylation of CpG sites located in the putative enhancer region between FADS1 and FADS2, in human liver tissue. However, this array only featured 20 CpG sites within this 12kb region. To better understand the methylation landscape within this region, we conducted bisulfite sequencing of the region between FADS1 and FADS2. Liver tissues from 50 male subjects (27 European Americans, 23 African Americans) were obtained from the Pathobiological Determinants of Atherosclerosis in Youth (PDAY) study, and used to ascertain the genotype at rs174537 and methylation status across the region of interest. Associations between rs174537 genotype and methylation status of 136 CpG sites were determined. Age-adjusted linear regressions were used to assess ASM associations with rs174537 genotype. The majority of CpG sites (117 out of 136, 86%) exhibited high levels of methylation with the greatest variability observed at three key regulatory regions–the promoter regions for FADS1 and FADS2 and a putative enhancer site between the two genes. Eight CpG sites within the putative enhancer region displayed significant (FDR p <0.05) ASM associations with rs174537. These data support the concept that both genetic and epigenetic factors regulate PUFA biosynthesis, and raise fundamental questions as to how genetic variants such as rs174537 impact DNA methylation in distant regulatory regions, and ultimately the capacity of tissues to synthesize PUFAs. Public Library of Science 2017-09-28 /pmc/articles/PMC5619705/ /pubmed/28957329 http://dx.doi.org/10.1371/journal.pone.0180903 Text en © 2017 Rahbar 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 (http://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
Rahbar, Elaheh
Ainsworth, Hannah C.
Howard, Timothy D.
Hawkins, Gregory A.
Ruczinski, Ingo
Mathias, Rasika
Seeds, Michael C.
Sergeant, Susan
Hixson, James E.
Herrington, David M.
Langefeld, Carl D.
Chilton, Floyd H.
Uncovering the DNA methylation landscape in key regulatory regions within the FADS cluster
title Uncovering the DNA methylation landscape in key regulatory regions within the FADS cluster
title_full Uncovering the DNA methylation landscape in key regulatory regions within the FADS cluster
title_fullStr Uncovering the DNA methylation landscape in key regulatory regions within the FADS cluster
title_full_unstemmed Uncovering the DNA methylation landscape in key regulatory regions within the FADS cluster
title_short Uncovering the DNA methylation landscape in key regulatory regions within the FADS cluster
title_sort uncovering the dna methylation landscape in key regulatory regions within the fads cluster
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5619705/
https://www.ncbi.nlm.nih.gov/pubmed/28957329
http://dx.doi.org/10.1371/journal.pone.0180903
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