精神分裂症患者超协调DNA甲基化改变与脑功能相关

Junfang Chen, Kristina Schwarz, Z. Zang, U. Braun, A. Harneit, T. Kremer, Ren Ma, J. Schweiger, C. Moessnang, Lena S. Geiger, Han Cao, F. Degenhardt, M. Nöthen, H. Tost, A. Meyer-Lindenberg, E. Schwarz
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摘要

DNA甲基化是一种表观遗传生物学过程,是环境风险对严重疾病(如精神分裂症)易感性影响的重要中介。DNA甲基化显示了生物相关基因之间的协调,但目前尚不清楚由此产生的网络结构是否对疾病风险有中介作用。在这里,我们发现了一个大型基因网络,在精神分裂症患者的大脑中改变了几个生物过程,这些过程与精神分裂症相关的大脑功能以及遗传疾病易感性相关。我们发现DNA甲基化在一个包含6399个基因的可重复网络中具有生理协调,并且在血液和大脑中显示出相似的结构。该网络在精神分裂症的核心重要生物学过程中高度协调,包括与精神分裂症最常见的遗传风险变异相关的突触过程。在精神分裂症供体的脑样本中,这些过程中的协同甲基化减少,并显示出与精神分裂症相关的脑功能存在年龄依赖性关联。这些结果支持DNA甲基化作为一种与精神分裂症相关的调节原则的协调,这种精神分裂症可能对特定发育时期的环境风险暴露和复合遗传疾病易感性敏感。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hyper-Coordinated DNA Methylation is Altered in Schizophrenia and Associated with Brain Function
DNA methylation is an epigenetic biological process that is emerging as an important mediator of environmental risk effects on the susceptibility of severe illness, such as schizophrenia. DNA methylation shows coordination across biologically-related genes, but it is not known whether the resulting network structure has a mediating effect on illness risk. Here we identified a large gene network with hyper-coordinated DNA methylation in several biological processes that are changed in the brain of patients with schizophrenia, and that are associated with schizophrenia-relevant brain function as well as genetic illness susceptibility. We found that DNA methylation was physiologically coordinated in a reproducible network that comprised 6399 genes and showed a similar architecture in blood and brain. The network was hyper-coordinated in biological processes of core importance for schizophrenia, including synaptic processes that are associated with the strongest common genetic risk variants for schizophrenia. Coordinated methylation in these processes was decreased in brain samples from donors with schizophrenia, and showed an age-dependent association with schizophrenia-relevant brain function. These results support the coordination of DNA methylation as a regulatory principle relevant to schizophrenia that may be sensitive to environmental risk exposure during specific developmental periods and compound genetic illness predisposition.
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