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酗酒者和对照组前额皮质的全球 DNA 启动子甲基化。

Global DNA promoter methylation in frontal cortex of alcoholics and controls.

机构信息

Department of Psychiatry and Behavioral Sciences, University of Kansas School of Medicine, Kansas City, KS 66160, USA.

出版信息

Gene. 2012 Apr 25;498(1):5-12. doi: 10.1016/j.gene.2012.01.096. Epub 2012 Feb 13.

DOI:10.1016/j.gene.2012.01.096
PMID:22353363
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3653411/
Abstract

To determine if ethanol consumption and alcoholism cause global DNA methylation disturbances, we examined alcoholics and controls using methylation specific microarrays to detect all annotated gene and non-coding microRNA promoters and their CpG islands. DNA was isolated and immunoprecipitated from the frontal cortex of 10 alcoholics and 10 age and gender-matched controls then labeled prior to co-hybridization. A modified Kolmogorov-Smirnov test was used to predict differentially enriched regions (peaks) from log-ratio estimates of amplified vs input DNA. More than 180,000 targets were identified for each subject which correlated with >30,000 distinct, integrated peaks or high probability methylation loci. Peaks were mapped to regions near 17,810 separate annotated genes per subject representing hypothetical methylation targets. No global methylation differences were observed between the two subject groups with 80% genetic overlap, but extreme methylation was observed in both groups at specific loci corresponding with known methylated genes (e.g., H19) and potentially other genes of unknown methylation status. Methylation density patterns targeting CpG islands visually correlated with recognized chromosome banding. Our study provides insight into global epigenetic regulation in the human brain in relationship to controls and potentially novel targets for hypothesis generation and follow-up studies of alcoholism.

摘要

为了确定乙醇摄入和酗酒是否会导致全球 DNA 甲基化紊乱,我们使用甲基化特异性微阵列检查了酗酒者和对照组,以检测所有注释的基因和非编码 microRNA 启动子及其 CpG 岛。从 10 名酗酒者和 10 名年龄和性别匹配的对照者的额叶中分离并免疫沉淀 DNA,然后在共杂交之前进行标记。使用修正的 Kolmogorov-Smirnov 检验来预测对数比估计的扩增与输入 DNA 的差异富集区域(峰)。每个受试者的目标超过 180,000 个,与 30,000 多个不同的、整合的峰或高概率甲基化位点相关。峰映射到每个受试者附近的 17,810 个单独注释基因的区域,代表假设的甲基化靶标。两个受试者组之间没有观察到全局甲基化差异,遗传重叠率为 80%,但在两个组中都观察到了特定位点的极端甲基化,这些位点与已知的甲基化基因(例如 H19)和潜在的其他未知甲基化状态的基因相对应。针对 CpG 岛的甲基化密度模式与公认的染色体带型视觉上相关。我们的研究提供了人类大脑中与对照相关的全局表观遗传调控的见解,并为酗酒的假说生成和后续研究提供了潜在的新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fbe/3653411/c4b4a6b89332/nihms360482f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fbe/3653411/bee26bb55385/nihms360482f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fbe/3653411/16015723f063/nihms360482f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fbe/3653411/2ac636221b96/nihms360482f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fbe/3653411/c4b4a6b89332/nihms360482f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fbe/3653411/bee26bb55385/nihms360482f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fbe/3653411/16015723f063/nihms360482f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fbe/3653411/2ac636221b96/nihms360482f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fbe/3653411/c4b4a6b89332/nihms360482f4.jpg

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