Li Xiaogang, Shi Xinxin, Gong Yin, Guo Wenting, Liu Yuanrui, Peng Chunwei, Xu Yingchun
Department of Clinical Laboratory, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.
Medical Research Center, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.
Front Genet. 2021 Nov 17;12:749211. doi: 10.3389/fgene.2021.749211. eCollection 2021.
5-Hydroxymethylcytosine (5hmC), the oxidative product of 5-methylcytosine (5mC) catalyzed by ten-eleven translocation enzymes, plays an important role in many biological processes as an epigenetic mediator. Prior studies have shown that 5hmC can be selectively labeled with chemically modified glucose moieties and enriched using click chemistry with biotin affinity approaches. Besides, DNA deaminases of the AID/APOBEC family can discriminate modified 5hmC bases from cytosine (C) or 5mC. Herein, we developed a method based on embryonic stem cell (ESC) whole-genome analysis, which could enrich 5hmC-containing DNA by selective chemical labeling and locate 5hmC sites at single-base resolution with enzyme-based deamination. The combination experimental design is an extension of previous methods, and we hope that this cost-effective single-base resolution 5hmC sequencing method could be used to promote the mechanism and diagnosis research of 5hmC.
5-羟甲基胞嘧啶(5hmC)是由TET酶催化的5-甲基胞嘧啶(5mC)的氧化产物,作为一种表观遗传介质在许多生物学过程中发挥重要作用。先前的研究表明,5hmC可以用化学修饰的葡萄糖部分进行选择性标记,并使用生物素亲和方法通过点击化学进行富集。此外,AID/APOBEC家族的DNA脱氨酶可以区分修饰的5hmC碱基与胞嘧啶(C)或5mC。在此,我们开发了一种基于胚胎干细胞(ESC)全基因组分析的方法,该方法可以通过选择性化学标记富集含5hmC的DNA,并通过基于酶的脱氨作用在单碱基分辨率下定位5hmC位点。这种组合实验设计是先前方法的扩展,我们希望这种具有成本效益的单碱基分辨率5hmC测序方法能够用于推动5hmC的机制和诊断研究。