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基因组DNA中5-羟甲基胞嘧啶的光谱定量分析。

Spectroscopic quantification of 5-hydroxymethylcytosine in genomic DNA.

作者信息

Shahal Tamar, Gilat Noa, Michaeli Yael, Redy-Keisar Orit, Shabat Doron, Ebenstein Yuval

机构信息

Raymond and Beverly Sackler Faculty of Exact Sciences, School of Chemistry, Tel Aviv University , Tel Aviv, 6997801, Israel.

出版信息

Anal Chem. 2014 Aug 19;86(16):8231-7. doi: 10.1021/ac501609d. Epub 2014 Jul 29.

Abstract

5-Hydroxymethylcytosine (5hmC), a modified form of the DNA base cytosine, is an important epigenetic mark linked to regulation of gene expression in development, and tumorigenesis. We have developed a spectroscopic method for a global quantification of 5hmC in genomic DNA. The assay is performed within a multiwell plate, which allows simultaneous recording of up to 350 samples. Our quantification procedure of 5hmC is direct, simple, and rapid. It relies on a two-step protocol that consists of enzymatic glucosylation of 5hmC with an azide-modified glucose, followed by a "click reaction" with an alkyne-fluorescent tag. The fluorescence intensity recorded from the DNA sample is proportional to its 5hmC content and can be quantified by a simple plate reader measurement. This labeling technique is specific and highly sensitive, allowing detection of 5hmC down to 0.002% of the total nucleotides. Our results reveal significant variations in the 5hmC content obtained from different mouse tissues, in agreement with previously reported data.

摘要

5-羟甲基胞嘧啶(5hmC)是DNA碱基胞嘧啶的一种修饰形式,是一种重要的表观遗传标记,与发育和肿瘤发生过程中的基因表达调控有关。我们开发了一种用于基因组DNA中5hmC全局定量的光谱方法。该测定在多孔板中进行,可同时记录多达350个样品。我们对5hmC的定量程序直接、简单且快速。它依赖于一个两步方案,该方案包括用叠氮化物修饰的葡萄糖对5hmC进行酶促糖基化,然后与炔烃荧光标签进行“点击反应”。从DNA样品记录的荧光强度与其5hmC含量成正比,可通过简单的酶标仪测量进行定量。这种标记技术具有特异性且高度灵敏,能够检测低至总核苷酸0.002%的5hmC。我们的结果显示,从不同小鼠组织获得的5hmC含量存在显著差异,这与先前报道的数据一致。

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