These authors contributed equally to this paper.
Methods Appl Fluoresc. 2016 Oct 7;4(4):044003. doi: 10.1088/2050-6120/4/4/044003.
The nucleobase 5-hydroxymethylcytosine (5-hmC), a modified form of cytosine, is an important epigenetic mark related to regulation of gene expression. 5-hmC levels are highly dynamic during early development and are modulated during the progression of neurodegenerative disease and cancer. We describe a spectroscopic method for the global quantification of 5-hmC in genomic DNA. This method relies on the enzymatic glucosylation of 5-hmC, followed by a glucose oxidation step that results in the formation of aldehyde moieties that are covalently linked to a fluorescent reporter by oxime ligation. The fluorescence intensity of the labeled sample is directly proportional to its 5-hmC content. We show that this simple and cost-effective technique is suitable for quantification of 5-hmC content in different mouse tissues.
碱基 5-羟甲基胞嘧啶(5-hmC)是胞嘧啶的一种修饰形式,是与基因表达调控相关的重要表观遗传标记。5-hmC 水平在早期发育过程中高度动态,并在神经退行性疾病和癌症的进展过程中受到调节。我们描述了一种用于基因组 DNA 中 5-hmC 全局定量的光谱方法。该方法依赖于 5-hmC 的酶葡萄糖基化,随后是葡萄糖氧化步骤,导致醛部分形成,醛部分通过肟连接共价连接到荧光报告分子上。标记样品的荧光强度与其 5-hmC 含量成正比。我们表明,这种简单且具有成本效益的技术适用于不同小鼠组织中 5-hmC 含量的定量。