Academic Journal

Epigenome-Wide DNA Methylation in Hearing Ability:New Mechanisms for an Old Problem

التفاصيل البيبلوغرافية
العنوان: Epigenome-Wide DNA Methylation in Hearing Ability:New Mechanisms for an Old Problem
المؤلفون: Wolber, Lisa E., Steves, Claire J., Tsai, Pei-Chien, Deloukas, Panos, Spector, Tim D., Bell, Jordana T., Williams, Frances M. K.
المصدر: Wolber , L E , Steves , C J , Tsai , P-C , Deloukas , P , Spector , T D , Bell , J T & Williams , F M K 2014 , ' Epigenome-Wide DNA Methylation in Hearing Ability : New Mechanisms for an Old Problem ' , PL o S One , vol. 9 , no. 9 , e105729 . https://doi.org/10.1371/journal.pone.0105729
سنة النشر: 2014
المجموعة: King's College, London: Research Portal
مصطلحات موضوعية: MONOZYGOTIC TWINS, STICKLER-SYNDROME, HUMAN BRAIN, GENE, PATTERNS, PROTEIN, METHYLTRANSFERASES, ASSOCIATION, IMPAIRMENT, TISSUES
الوصف: Epigenetic regulation of gene expression has been shown to change over time and may be associated with environmental exposures in common complex traits. Age-related hearing impairment is a complex disorder, known to be heritable, with heritability estimates of 57-70%. Epigenetic regulation might explain the observed difference in age of onset and magnitude of hearing impairment with age. Epigenetic epidemiology studies using unrelated samples can be limited in their ability to detect small effects, and recent epigenetic findings in twins underscore the power of this well matched study design. We investigated the association between venous blood DNA methylation epigenome-wide and hearing ability. Pure-tone audiometry (PTA) and Illumina HumanMethylation array data were obtained from female twin volunteers enrolled in the TwinsUK register. Two study groups were explored: first, an epigenome-wide association scan (EWAS) was performed in a discovery sample (n = 115 subjects, age range: 47-83 years, Illumina 27 k array), then replication of the top ten associated probes from the discovery EWAS was attempted in a second unrelated sample (n = 203, age range: 41-86 years, Illumina 450 k array). Finally, a set of monozygotic (MZ) twin pairs (n = 21 pairs) within the discovery sample (Illumina 27 k array) was investigated in more detail in an MZ discordance analysis. Hearing ability was strongly associated with DNA methylation levels in the promoter regions of several genes, including TCF25 (cg01161216, p = 6.6x10(-6)), FGFR1 (cg15791248, p = 5.7x10(-5)) and POLE (cg18877514, p = 6.3x10(-5)). Replication of these results in a second sample confirmed the presence of differential methylation at TCF25 (p(replication) = 6x10(-5)) and POLE (p(replication) = 0.016). In the MZ discordance analysis, twins' intrapair difference in hearing ability correlated with DNA methylation differences at ACP6 (cg01377755, r = -0.75, p = 1.2x10(-4)) and MEF2D (cg08156349, r = -0.75, p = 1.4x10(-4)). Examination of gene expression in skin, ...
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1371/journal.pone.0105729
الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/6c0cfe8d-c551-473b-a20d-0b9a0ea19d3d
https://doi.org/10.1371/journal.pone.0105729
Rights: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.2F49F44E
قاعدة البيانات: BASE
الوصف
DOI:10.1371/journal.pone.0105729