Beijing National Laboratory for Molecular Sciences (BNLMS), MOE Key Laboratory of Bioorganic Chemistry and Molecular Engineering, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.
Anal Chem. 2022 Jun 7;94(22):8066-8074. doi: 10.1021/acs.analchem.2c01679. Epub 2022 May 25.
Oxidative DNA damage is tightly linked to the development of multiple age-related diseases. The prominent oxidation product is 8-oxo-7,8-dihydroguanine (OG), which has been proved to be an important epigenetic-like biomarker. Quantification of the locus-specific OG frequency includes quantitative and locating information, which is of great significance for exploring the functional roles of OG in disease induction and gene regulation. Herein, an ultrasensitive quantification of OG at single-base resolution was established using real-time fluorescence quantitative polymerase chain reaction as an amplification tool. Based on the coding property of DNA polymerase that incorporates adenine on the opposite site of OG and the selectivity of the ligase for perfectly matched sequences, the difference between OG and G on the sequence could be enlarged. Well-performed DNA ligase was selected out, and as low as 46.2 zmol of target DNA with an OG site and an OG frequency of 5% could be detected. G contents on a specific site were also detectable based on the similar principle, thus the OG frequency of this locus could be accurately determined by a standard addition method. This strategy was successfully applied to the evaluation of locus-specific OG in both model DNA and genomic DNA from human cervical carcinoma cell lines under multiple oxidative stress, showing the potential for functional research and dynamic monitoring of critical OG sites.
氧化 DNA 损伤与多种与年龄相关的疾病的发展密切相关。突出的氧化产物是 8-氧代-7,8-二氢鸟嘌呤(OG),它已被证明是一种重要的表观遗传样生物标志物。OG 频率的定位特异性定量包括定量和定位信息,这对于探索 OG 在疾病诱导和基因调控中的功能作用具有重要意义。在此,我们使用实时荧光定量聚合酶链反应作为扩增工具,建立了单碱基分辨率下 OG 的超灵敏定量方法。基于 DNA 聚合酶在 OG 对面掺入腺嘌呤的编码特性和连接酶对完全匹配序列的选择性,可以放大 OG 与 G 在序列上的差异。选择性能良好的 DNA 连接酶,即使是带有 OG 位点和 OG 频率为 5%的目标 DNA 低至 46.2 zmol 也可以被检测到。基于类似的原理,还可以检测特定位置上的 G 含量,因此可以通过标准添加法准确确定该基因座的 OG 频率。该策略成功应用于多种氧化应激下模型 DNA 和人宫颈癌细胞系基因组 DNA 中特定基因座 OG 的评估,显示了其在关键 OG 位点的功能研究和动态监测中的潜力。