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DNA Methylation and Susceptibility to Autism Spectrum Disorder

机译:DNA甲基化和自闭症谱系疾病的易感性

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The prevalence of autism spectrum disorder (ASD) has been increasing steadily over the last 20 years; however, the molecular basis for the majority of ASD cases remains unknown. Recent advances in next-generation sequencing and detection of DNA modifications have made methylation-dependent regulation of transcription an attractive hypothesis for being a causative factor in ASD etiology. Evidence for abnormal DNA methylation in ASD can be seen on multiple levels, from genetic mutations in epigenetic machinery to loci-specific and genome-wide changes in DNA methylation. Epimutations in DNA methylation can be acquired throughout life, as global DNA methylation reprogramming is dynamic during embryonic development and the early postnatal period that corresponds to the peak time of synaptogenesis. However, technical advances and causative evidence still need to be established before abnormal DNA methylation and ASD can be confidently associated.
机译:自闭症谱系障碍(ASD)的患病率在过去20年中一直在稳步增长; 然而,大多数ASD病例的分子基础仍然未知。 下一代测序和DNA修饰检测的最新进展使得甲基化依赖性调节转录的含有吸引性的假设,用于ASD病因中的致病因子。 在多个水平上可以看出ASD中异常DNA甲基化的证据,从表观遗传机制中的遗传突变到DNA甲基化的基因特异性和基因组的变化。 在整个寿命中可以获得DNA甲基化中的缩影,因为全局DNA甲基化重编程在胚胎发育期间和对应于突触峰值时间的早期后期。 然而,在异常DNA甲基化并且ASD可以自信相关之前需要建立技术进步和致病证据。

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