阿尔茨海默病中 DNA 和 RNA 的表观遗传修饰

Paula Martínez-Feduchi, Peng Jin, Bing Yao
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引用次数: 0

摘要

阿尔茨海默病(AD)是一种复杂的神经退行性疾病,也是最常见的痴呆症。阿尔茨海默病主要有两种类型:家族性和散发性。家族性 AD 与淀粉样前体蛋白(APP)、早老素-1(PSEN1)和早老素-2(PSEN2)的突变有关。另一方面,散发性注意力缺失症是更常见的疾病形式,其遗传、表观遗传和环境因素都会影响疾病的发生和发展。研究与注意力缺失症相关的表观遗传学机制对于加深对病理的理解以及确定诊断和治疗的生物标志物至关重要。DNA 和 RNA 上的化学共价修饰可在转录和转录后水平对基因表达进行表观遗传调控,并在注意力缺失症和其他神经退行性疾病中发挥保护或病理作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epigenetic modifications of DNA and RNA in Alzheimer’s disease
Alzheimer’s disease (AD) is a complex neurodegenerative disorder and the most common form of dementia. There are two main types of AD: familial and sporadic. Familial AD is linked to mutations in amyloid precursor protein (APP), presenilin-1 (PSEN1), and presenilin-2 (PSEN2). On the other hand, sporadic AD is the more common form of the disease and has genetic, epigenetic, and environmental components that influence disease onset and progression. Investigating the epigenetic mechanisms associated with AD is essential for increasing understanding of pathology and identifying biomarkers for diagnosis and treatment. Chemical covalent modifications on DNA and RNA can epigenetically regulate gene expression at transcriptional and post-transcriptional levels and play protective or pathological roles in AD and other neurodegenerative diseases.
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