Charcot-Marie-Tooth Disease 1A 型患者神经和应激相关基因甲基化水平的比较分析

Da Eun Nam, Seon Hyeok Hwang, Jun Yeop Yim, Byung-Ok Choi, Ki Wha Chung
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引用次数: 0

摘要

背景:Charcot-Marie-Tooth 病 1A 型(CMT1A)是由包括 PMP22 基因在内的 17p12 区域重复引起的。有报道称,在 CMT1A 患者中,预示着严重程度会逐代增加。也有报道称,非新生病例的严重程度比新生病例的严重程度要高。本研究旨在检测 CMT1A 病例与对照组之间以及新生病例与非新生病例之间的表观遗传学差异:本研究调查了 40 名韩国 CMT1A 患者和 11 名对照组。使用 SureSelect XT Methyl-Seq 试剂盒和亚硫酸氢盐序列映射程序测定甲基化水平:结果:在病例与对照组之间、新发病例与非新发病例之间的比较中,发现了许多不同的甲基化 CpG 位点(DMCs)。大多数 DMC 位于与神经系统、精神压力和运动能力相关的基因内或附近:本研究是首个揭示 CMT1A 患者临床异质性机制的表观遗传学研究。我们认为,新发病例的严重程度弱于非新发病例,可能与神经和应激相关基因的表观基因组差异有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Analysis on Methylation Levels of Nerve and Stress Related Genes in Charcot-Marie-Tooth Disease Type 1A Patients
Background: Charcot-Marie-Tooth disease type 1A (CMT1A) is caused by duplication of the 17p12 region including PMP22 gene. In CMT1A patients, anticipation showing increased severity by generations has been reported in the CMT1A patients. It has also been reported that severity increases in the non-de novo cases than in the de novo cases. This study was performed to examine epigenetic differences between CMT1A cases and controls as well as between de novo cases and non-de novo cases.Methods: This study examined 40 Korean CMT1A patients and 11 controls. Methylation level was determined using the SureSelect XT Methyl-Seq reagent kit and bisulfite sequence mapping program.Results: Many differentially methylated CpG sites (DMCs) were identified in the comparisonbetween cases and controls and between de novo cases and non-de novo cases. Most DMCs were located within or nearby genes related to the nervous system, mental stress, and motor ability.Conclusions: This study is the first epigenetic study to uncover the mechanism of clinical heterogeneity among CMT1A patients. We suggest that weak severity in the de novo cases than the non-de novo cases may be related to the epigenomic differences in the nerve and stress-related genes.
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