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Whole-Genome Differentially Hydroxymethylated DNA Regions among Twins Discordant for Cardiovascular Death

Epigenetics is a mechanism underlying cardiovascular disease. It is unknown whether DNA hydroxymethylation is prospectively associated with the risk for cardiovascular death independent of germline and common environment. Male twin pairs middle-aged in 1969–1973 and discordant for cardiovascular dea...

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Autores principales: Dai, Jun, Leung, Ming, Guan, Weihua, Guo, Han-Tian, Krasnow, Ruth E., Wang, Thomas J., El-Rifai, Wael, Zhao, Zhongming, Reed, Terry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8392630/
https://www.ncbi.nlm.nih.gov/pubmed/34440357
http://dx.doi.org/10.3390/genes12081183
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author Dai, Jun
Leung, Ming
Guan, Weihua
Guo, Han-Tian
Krasnow, Ruth E.
Wang, Thomas J.
El-Rifai, Wael
Zhao, Zhongming
Reed, Terry
author_facet Dai, Jun
Leung, Ming
Guan, Weihua
Guo, Han-Tian
Krasnow, Ruth E.
Wang, Thomas J.
El-Rifai, Wael
Zhao, Zhongming
Reed, Terry
author_sort Dai, Jun
collection PubMed
description Epigenetics is a mechanism underlying cardiovascular disease. It is unknown whether DNA hydroxymethylation is prospectively associated with the risk for cardiovascular death independent of germline and common environment. Male twin pairs middle-aged in 1969–1973 and discordant for cardiovascular death through December 31, 2014, were included. Hydroxymethylation was quantified in buffy coat DNA collected in 1986–1987. The 1893 differentially hydroxymethylated regions (DhMRs) were identified after controlling for blood leukocyte subtypes and age among 12 monozygotic (MZ) pairs (Benjamini–Hochberg False Discovery Rate < 0.01), of which the 102 DhMRs were confirmed with directionally consistent log(2)-fold changes and p < 0.01 among additional 7 MZ pairs. These signature 102 DhMRs, independent of the germline, were located on all chromosomes except for chromosome 21 and the Y chromosome, mainly within/overlapped with intergenic regions and introns, and predominantly hyper-hydroxymethylated. A binary linear classifier predicting cardiovascular death among 19 dizygotic pairs was identified and equivalent to that generated from MZ via the 2D transformation. Computational bioinformatics discovered pathways, phenotypes, and DNA motifs for these DhMRs or their subtypes, suggesting that hydroxymethylation was a pathophysiological mechanism underlying cardiovascular death that might be influenced by genetic factors and warranted further investigations of mechanisms of these signature regions in vivo and in vitro.
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spelling pubmed-83926302021-08-28 Whole-Genome Differentially Hydroxymethylated DNA Regions among Twins Discordant for Cardiovascular Death Dai, Jun Leung, Ming Guan, Weihua Guo, Han-Tian Krasnow, Ruth E. Wang, Thomas J. El-Rifai, Wael Zhao, Zhongming Reed, Terry Genes (Basel) Article Epigenetics is a mechanism underlying cardiovascular disease. It is unknown whether DNA hydroxymethylation is prospectively associated with the risk for cardiovascular death independent of germline and common environment. Male twin pairs middle-aged in 1969–1973 and discordant for cardiovascular death through December 31, 2014, were included. Hydroxymethylation was quantified in buffy coat DNA collected in 1986–1987. The 1893 differentially hydroxymethylated regions (DhMRs) were identified after controlling for blood leukocyte subtypes and age among 12 monozygotic (MZ) pairs (Benjamini–Hochberg False Discovery Rate < 0.01), of which the 102 DhMRs were confirmed with directionally consistent log(2)-fold changes and p < 0.01 among additional 7 MZ pairs. These signature 102 DhMRs, independent of the germline, were located on all chromosomes except for chromosome 21 and the Y chromosome, mainly within/overlapped with intergenic regions and introns, and predominantly hyper-hydroxymethylated. A binary linear classifier predicting cardiovascular death among 19 dizygotic pairs was identified and equivalent to that generated from MZ via the 2D transformation. Computational bioinformatics discovered pathways, phenotypes, and DNA motifs for these DhMRs or their subtypes, suggesting that hydroxymethylation was a pathophysiological mechanism underlying cardiovascular death that might be influenced by genetic factors and warranted further investigations of mechanisms of these signature regions in vivo and in vitro. MDPI 2021-07-29 /pmc/articles/PMC8392630/ /pubmed/34440357 http://dx.doi.org/10.3390/genes12081183 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dai, Jun
Leung, Ming
Guan, Weihua
Guo, Han-Tian
Krasnow, Ruth E.
Wang, Thomas J.
El-Rifai, Wael
Zhao, Zhongming
Reed, Terry
Whole-Genome Differentially Hydroxymethylated DNA Regions among Twins Discordant for Cardiovascular Death
title Whole-Genome Differentially Hydroxymethylated DNA Regions among Twins Discordant for Cardiovascular Death
title_full Whole-Genome Differentially Hydroxymethylated DNA Regions among Twins Discordant for Cardiovascular Death
title_fullStr Whole-Genome Differentially Hydroxymethylated DNA Regions among Twins Discordant for Cardiovascular Death
title_full_unstemmed Whole-Genome Differentially Hydroxymethylated DNA Regions among Twins Discordant for Cardiovascular Death
title_short Whole-Genome Differentially Hydroxymethylated DNA Regions among Twins Discordant for Cardiovascular Death
title_sort whole-genome differentially hydroxymethylated dna regions among twins discordant for cardiovascular death
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8392630/
https://www.ncbi.nlm.nih.gov/pubmed/34440357
http://dx.doi.org/10.3390/genes12081183
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