《生命科学》 2018, 30(4): 374-382
摘 要:摘 要:DNA 甲基化是真核生物的重要表观遗传修饰,如胞嘧啶C5位甲基化5-甲基胞嘧啶(5mC)和腺嘌呤N6 位甲基化6-甲基腺嘌呤(6mA)。DNA 5mC可经Tet双加氧酶催化氧化形成5-羟甲基胞嘧啶(5hmC)、5-醛甲基胞嘧啶(5fC) 和5-羧基胞嘧啶(5caC)。这些氧化产物不仅是去甲基化过程的中间体,而且也可能存在各自特有的表观调控功能。其中,5hmC 异常可能和癌症相关,有可能成为疾病诊断的生物标志物。发展可靠、高灵敏和抗干扰能力强的DNA 甲基化和去甲基化检测技术和方法至关重要,有助于理解甲基化和去甲基化的分子机制以及提高肿瘤的诊断水平。现针对DNA 甲基化和去甲基化检测技术进行简要介绍。
Abstract: Abstract: Eukaryotic DNA methylations, including methylation of C5 position of cytosine 5-methylcytosine (5mC) and N6 position of adenine (6-methyladenine, 6mA), are critical and important epigenetic markers. DNA 5mC can be oxidized to form three intermediates, 5-hydroxymethylcytosine (5hmC), 5-formylcytosine (5fC), 5-carboxylcytosine (5caC), as catalized by Tet family dioxygenases. In addition to being as demethylation intermediates, 5hmC content is negatively correlated with tumor occurrence, and thus is a potential biomarker indicating occurrence and development of tumors. To understand these events and underlying mechanisms, it is essential to develop reliable, sensitive and interference-free methods for detection of DNA methylation and demethylation. Here we briefly review and discuss analytical and sequencing technologies for detection of epigenetic modifications involved in DNA methylation and demethylation.