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帕金森病皮质DNA甲基化的全表观基因组分析

Epigenome-Wide Analysis of DNA Methylation in Parkinson's Disease Cortex.

作者信息

Kaut Oliver, Schmitt Ina, Stahl Fabian, Fröhlich Holger, Hoffmann Per, Gonzalez Frank J, Wüllner Ullrich

机构信息

Department of Neurology, University of Bonn, 53105 Bonn, Germany.

DZNE (Deutsches Zentrum für Neurodegenerative Erkrankungen), 53105 Bonn, Germany.

出版信息

Life (Basel). 2022 Mar 29;12(4):502. doi: 10.3390/life12040502.

Abstract

Background: Epigenetic factors including DNA methylation contribute to specific patterns of gene expression. Gene−environment interactions can change the methylation status in the brain, and accumulation of these epigenetic changes over a lifespan may be co-responsible for a neurodegenerative disease like Parkinson’s disease, which that is characterised by a late onset in life. Aims: To determine epigenetic modifications in the brains of Parkinson’s disease patients. Patients and Methods: DNA methylation patterns were compared in the cortex tissue of 14 male PD patients and 10 male healthy individuals using the Illumina Methylation 450 K chip. Subsequently, DNA methylation of candidate genes was evaluated using bisulphite pyrosequencing, and DNA methylation of cytochrome P450 2E1 (CYP2E1) was characterized in DNA from blood mononuclear cells (259 PD patients and 182 healthy controls) and skin fibroblasts (10 PD patients and 5 healthy controls). Protein levels of CYP2E1 were analysed using Western blot in human cortex and knock-out mice brain samples. Results: We found 35 hypomethylated and 22 hypermethylated genes with a methylation M-value difference >0.5. Decreased methylation of cytochrome P450 2E1 (CYP2E1) was associated with increased protein levels in PD brains, but in peripheral tissues, i.e., in blood cells and skin fibroblasts, DNA methylation of CYP2E1 was unchanged. In CYP2E1 knock-out mice brain alpha-synuclein (SNCA) protein levels were down-regulated compared to wild-type mice, whereas treatment with trichloroethylene (TCE) up-regulated CYP2E1 protein in a dose-dependent manner in cultured cells. We further identified an interconnected group of genes associated with oxidative stress, such as Methionine sulfoxide reductase A (MSRA) and tumour protein 73 (TP73) in the brain, which again were not paralleled in other tissues and appeared to indicate brain-specific changes. Conclusions: Our study revealed surprisingly few dysmethylated genes in a brain region less affected in PD. We confirmed hypomethylation of CYP2E1.

摘要

背景

包括DNA甲基化在内的表观遗传因素有助于特定的基因表达模式。基因与环境的相互作用可改变大脑中的甲基化状态,而这些表观遗传变化在整个生命周期中的积累可能共同导致诸如帕金森病等神经退行性疾病,其特征为发病较晚。目的:确定帕金森病患者大脑中的表观遗传修饰。患者和方法:使用Illumina甲基化450K芯片比较14名男性帕金森病患者和10名男性健康个体皮质组织中的DNA甲基化模式。随后,使用亚硫酸氢盐焦磷酸测序评估候选基因的DNA甲基化,并对来自血液单核细胞(259名帕金森病患者和182名健康对照)和皮肤成纤维细胞(10名帕金森病患者和5名健康对照)的DNA中的细胞色素P450 2E1(CYP2E1)的DNA甲基化进行表征。使用蛋白质印迹法分析人皮质和基因敲除小鼠脑样本中CYP2E1的蛋白质水平。结果:我们发现35个低甲基化基因和22个高甲基化基因,甲基化M值差异>0.5。细胞色素P450 2E1(CYP2E1)甲基化降低与帕金森病大脑中蛋白质水平升高相关,但在外周组织,即血细胞和皮肤成纤维细胞中,CYP2E1的DNA甲基化未发生变化。在CYP2E1基因敲除小鼠大脑中,α-突触核蛋白(SNCA)蛋白质水平与野生型小鼠相比下调,而在培养细胞中,用三氯乙烯(TCE)处理以剂量依赖性方式上调CYP2E1蛋白质。我们进一步鉴定了一组与氧化应激相关的相互关联的基因,如大脑中的甲硫氨酸亚砜还原酶A(MSRA)和肿瘤蛋白73(TP73),这些基因在其他组织中并未出现类似情况,似乎表明是大脑特异性变化。结论:我们的研究显示,在帕金森病中受影响较小的脑区中,甲基化异常的基因出奇地少。我们证实了CYP2E1的低甲基化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0883/9025601/344e783f2b53/life-12-00502-g001.jpg

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