Liu Xi, Ou Shu, Xu Tao, Liu Shiyong, Yuan Jinxian, Huang Hao, Qin Lu, Yang Hui, Chen Lifen, Tan Xinjie, Chen Yangmei
Department of Neurology, The Second Affiliated Hospital of Chongqing Medical University, Yuzhong District, Chongqing, 400010, China.
Epilepsy Center of PLA, Department of Neurosurgery, Xinqiao Hospital, The Third Military Medical University, Shapingba District, Chongqing, 400037, China.
Oncotarget. 2016 Dec 27;7(52):87402-87416. doi: 10.18632/oncotarget.13642.
Epigenetics underlying refractory epilepsy is poorly understood, especially in patients without distinctive genetic alterations. DNA methylation may affect gene expression in epilepsy without affecting DNA sequences. Herein, we analyzed genome-wide DNA methylation and gene expression in brain tissues of 10 patients with refractory epilepsy using methylated DNA immunoprecipitation linked with sequencing and mRNA Sequencing. Diverse distribution of differentially methylated genes was found in X chromosome, while differentially methylated genes appeared rarely in Y chromosome. 62 differentially expressed genes, such as MMP19, AZGP1, DES, and LGR6 were correlated with refractory epilepsy for the first time. Although general trends of differentially enriched gene ontology terms and Kyoto Encyclopedia of Genes and Genome pathways in this study are consistent with previous researches, differences also exist in many specific gene ontology terms and Kyoto Encyclopedia of Genes and Genome pathways. These findings provide a new genome-wide profiling of DNA methylation and gene expression in brain tissues of patients with refractory epilepsy, which may provide a basis for further study on the etiology and mechanisms of refractory epilepsy.
难治性癫痫背后的表观遗传学机制尚不清楚,尤其是在没有明显基因改变的患者中。DNA甲基化可能在不影响DNA序列的情况下影响癫痫中的基因表达。在此,我们使用甲基化DNA免疫沉淀测序和mRNA测序分析了10例难治性癫痫患者脑组织中的全基因组DNA甲基化和基因表达。在X染色体上发现了差异甲基化基因的不同分布,而在Y染色体上差异甲基化基因很少出现。62个差异表达基因,如MMP19、AZGP1、DES和LGR6,首次与难治性癫痫相关。虽然本研究中差异富集的基因本体术语和京都基因与基因组百科全书途径的总体趋势与先前研究一致,但在许多特定的基因本体术语和京都基因与基因组百科全书途径中也存在差异。这些发现提供了难治性癫痫患者脑组织中DNA甲基化和基因表达的新的全基因组图谱,这可能为难治性癫痫的病因和机制的进一步研究提供基础。