Epilepsy is a frequent neurological disorder, although onset and progression of seizures remain difficult to predict in affected patients, irrespective of their epileptogenic condition. Previous studies in animal models as well as human epileptic brain tissue revealed a remarkably diverse pattern of gene expression implicating epigenetic changes to contribute to disease progression. Here we mapped for the first time global DNA methylation patterns in chronic epileptic rats and controls. Using methyl-CpG capture associated with massive parallel sequencing (Methyl-Seq) we report the genomic methylation signature of the chronic epileptic state. We observed a predominant increase, rather than loss of DNA methylation in chronic rat epilepsy. Aberrant methylation patterns were inversely correlated with gene expression changes using mRNA sequencing from same animals and tissue specimens. Administration of a ketogenic, high-fat, low-carbohydrate diet attenuated seizure progression and ameliorated DNA methylation mediated changes in gene expression. This is the first report of unsupervised clustering of an epigenetic mark being used in epilepsy research to separate epileptic from non-epileptic animals as well as from animals receiving anti-convulsive dietary treatment. We further discuss the potential impact of epigenetic changes as a pathogenic mechanism of epileptogenesis.

译文

癫痫是一种常见的神经系统疾病,尽管无论发病情况如何,癫痫发作的发作和进展仍难以预测。先前在动物模型以及人类癫痫脑组织中的研究揭示了一种非常不同的基因表达模式,这些基因表达涉及表观遗传变化,从而导致疾病进展。在这里,我们首次绘制了慢性癫痫大鼠和对照组的全球DNA甲基化模式。使用与大规模平行测序 (methyl-Seq) 相关的甲基-CpG捕获,我们报告了慢性癫痫状态的基因组甲基化特征。我们观察到慢性大鼠癫痫的主要增加,而不是DNA甲基化的丧失。使用来自相同动物和组织标本的mRNA测序,异常甲基化模式与基因表达变化呈负相关。给予生酮,高脂,低碳水化合物饮食可减轻癫痫发作的进展,并改善DNA甲基化介导的基因表达变化。这是在癫痫研究中使用无监督的表观遗传标记聚类的第一份报告,该遗传标记用于将癫痫与非癫痫动物以及接受抗惊厥饮食治疗的动物分开。我们进一步讨论了表观遗传变化作为癫痫发生的致病机制的潜在影响。

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