Genome-wide DNA methylation patterns in discordant sib pairs with alcohol dependence
Introduction Alcohol dependence is a complex disease caused by a confluence of environmental and genetic factors. Epigenetic mechanisms have been shown to play an important role in the pathogenesis of alcohol dependence. Methods To determine if alterations in gene‐specific methylation were associate...
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Published in | Asia-Pacific psychiatry Vol. 5; no. 1; pp. 39 - 50 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Australia
Blackwell Publishing Ltd
01.03.2013
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Introduction
Alcohol dependence is a complex disease caused by a confluence of environmental and genetic factors. Epigenetic mechanisms have been shown to play an important role in the pathogenesis of alcohol dependence.
Methods
To determine if alterations in gene‐specific methylation were associated with alcohol dependence, a genome‐wide DNA methylation analysis was performed on peripheral blood mononuclear cells from alcohol‐dependent patients and siblings without alcohol dependence as controls. The Illumina Infinium Human Methylation450 BeadChip was used and gene‐specific methylation of DNA isolated from peripheral blood mononuclear cells was assessed. Genes ALDH1L2, GAD1, DBH and GABRP were selected to validate beadchip results by pyrosequencing.
Results
Compared to normal controls, 865 hypomethylated and 716 hypermethylated CG sites in peripheral blood mononuclear cell DNA in alcohol‐dependent patients were identified. The most hypomethylated CG site is located in the promoter of SSTR4 (somatostatin receptor 4) and the most hypermethylated CG site is GABRP (gamma‐aminobutyric acid A receptor). The results from beadchip analysis were consistent with that of pyrosequencing.
Discussion
DNA methylation might be associated with alcohol dependence. Genes SSTR4, ALDH1L2, GAD1, DBH and GABRP may participate in the biological process of alcohol dependence. |
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Bibliography: | National Key Basic Research and Development Program (973) - No. 2009CB522007 Henan Science Technology Committee - No. 094200510005 ark:/67375/WNG-Q73Q22MZ-4 istex:7EFBABDF188F3AB3D8EA4E3642387D28BE322EFD Table S1. (a) Thirty top-ranked hypomethylated genes. (b) Thirty top-ranked hypermethylated genes. ArticleID:APPY12010 Fund for Talents with Innovation in Medical Science and Technology of Henan Province - No. 3052 National Natural Science Foundation of China - No. 81171261 Major Program of National Natural Science Foundation of China - No. 20111483 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1758-5864 1758-5872 |
DOI: | 10.1111/appy.12010 |