伊斯法罕人群中的RORA和自闭症:是否存在表观遗传关系

Mansoor Salehi, E. Kamali, M. Karahmadi, S. M. Mousavi
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引用次数: 11

摘要

目的自闭症是一种以语言和非语言交流困难、社交障碍、行为受限和重复为特征的神经发育障碍。它最近被介绍为一种多基因疾病,其病理上具有显著的表观遗传效应。最近,维甲酸受体相关孤儿受体α (RORα)基因(在神经组织发育中起重要作用)的表观遗传沉默被证明发生在自闭症儿童中,原因是其启动子区域甲基化。这也许可以解释自闭症的分子发病机制的一个重要部分。因此,我们旨在通过在伊斯法罕人群中实施病例对照(实验)研究来证实这一发现。材料和方法采用熔融曲线分析-甲基化(MCA-Meth)方法,对30例亚硫酸氢钠治疗后自闭症儿童淋巴细胞中RORA启动子区(-200 ~ -64位)GpG岛(包含13个CpG位点)136bp序列的甲基化状态进行了实验研究,并与正常儿童进行了比较。此外,定量逆转录-聚合酶链反应(qRT-PCR)分析用于估计mRNA转录物水平并评估MCA-Meth分析结果。结果本研究显示,自闭症和正常儿童的启动子区域没有甲基化,所有研究样本的融化曲线与未甲基化的对照组相当。MCA-Meth分析结果也与qRT-PCR结果一致。因此,我们观察到自闭症儿童和健康儿童血液淋巴细胞中RORα转录物水平无显著差异。结论RORA启动子区的甲基化可能不是所有人群自闭症的共同表观遗传危险因素。因此,自闭症的分子发病机制在被调查人群中仍不清楚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RORA and Autism in The Isfahan Population: Is There An Epigenetic Relationship
Objective Autism is a neurodevelopmental disorder characterized by difficulty in verbal and non-verbal communication, impaired social interaction, and restricted and repetitive behavior. It has been recently introduced as a multigenic disorder with significant epigenetic effects on its pathology. Recently, epigenetic silencing of retinoic acid receptor- related orphan receptor alpha (RORα) gene (which has an essential role in neural tissue development) was shown to have occurred in autistic children due to methylation of its promoter region. This may thus explain a significant part of the molecular pathogenesis of autism. Therefore, we aimed to confirm this finding by implementing a case-control (experimental) study in the population of Isfahan. Materials and Methods The methylation status of a 136 bp sequence of a GpG island (encompassing 13 CpG sites) in the RORA promoter region (positions -200 to -64) as an experimental study was examined in the lymphocyte cells of 30 autistic children after sodium bisulfite treatment using the melting curve analysis-methylation (MCA-Meth) assay compared with normal children. Also, quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) analysis was used to estimate the level of mRNA transcripts and to evaluate MCA-Meth analysis results. Results This study revealed no methylation in the examined promoter regions in both autistic and normal children, with the melting curve of all studied samples being comparable to that of the non-methylated control. The results of MCA-Meth analysis were also consistent with qRT-PCR results. We therefore observed no significant difference in the levels of RORα transcripts in the blood lymphocytes between autistic and healthy children. Conclusion The methylation of the RORA promoter region may not be considered as a common epigenetic risk factor for autism in all populations. Hence, the molecular pathogenesis of autism remains unclear in the population investigated.
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