University of Exeter Medical School, College of Medicine and Health, Exeter University, Exeter, UK.
Neuropathol Appl Neurobiol. 2020 Dec;46(7):641-653. doi: 10.1111/nan.12650. Epub 2020 Aug 30.
In late 2014, the first epigenome-wide association studies of DNA modifications in Alzheimer's disease brain samples were published. Over the last 5 years, further studies have been reported in the field and have highlighted consistent and robust alterations in DNA modifications in AD cortex. However, there are some caveats associated with the majority of studies undertaken to date; for example, they are predominantly restricted to profiling a limited number of loci, are principally focused on DNA methylation, are performed on bulk tissue at the end stage of disease and are restricted to nominating associations rather than demonstrating causal relationships. Consequently, the downstream interpretation of these studies is limited. Owing to recent advances in state-of-the-art cell profiling techniques, long-read genomic technologies and genetic engineering methodologies, identifying cell-type-specific causal epigenetic changes is becoming feasible. This review seeks to provide an overview of the last 5 years of epigenomic studies of DNA modifications in Alzheimer's disease brain samples and propose new avenues for future research.
2014 年末,首次发表了针对阿尔茨海默病大脑样本中 DNA 修饰的全基因组关联研究。在过去的 5 年中,该领域又有进一步的研究报告,并强调了 AD 皮质中 DNA 修饰的一致和稳健改变。然而,与迄今为止进行的大多数研究相关的一些警告;例如,它们主要局限于对有限数量的基因座进行分析,主要集中在 DNA 甲基化上,在疾病的晚期对大块组织进行分析,并且仅限于提名关联而不是证明因果关系。因此,这些研究的下游解释受到限制。由于最先进的细胞分析技术、长读基因组技术和基因工程方法的最新进展,确定细胞类型特异性的因果性表观遗传变化变得可行。本综述旨在概述过去 5 年中阿尔茨海默病大脑样本中 DNA 修饰的表观基因组研究,并为未来的研究提出新的途径。