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首页> 外文期刊>Bioorganic and medicinal chemistry >Simple and accurate single base resolution analysis of 5-hydroxymethylcytosine by catalytic oxidative bisulfite sequencing using micelle incarcerated oxidants
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Simple and accurate single base resolution analysis of 5-hydroxymethylcytosine by catalytic oxidative bisulfite sequencing using micelle incarcerated oxidants

机译:用胶束甲状腺素测序催化氧化亚硫酸氢盐测定简单且精确的单碱谱分辨率分析分辨率分析分辨率分析分辨率。

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摘要

Oxidation of 5-methylcytosine (5mC) is catalyzed by ten-eleven translocation (TET) enzymes to produce 5-hydroxymethylcytosine (5hmC) and following oxidative products. The oxidized nucleotides were shown to be the intermediates for DNA demethylation, as the nucleotides are removed by base excision repair system initiated by thymine DNA glycosylase. A simple and accurate method to determine initial oxidation product 5hmC at single base resolution in genomic DNA is necessary to understand demethylation mechanism. Recently, we have developed a new catalytic oxidation reaction using micelle-incarcerated oxidants to oxidize 5hmC to form 5-formylcytosine (5fC), and subsequent bisulfite sequencing can determine the positions of 5hmC in DNA. In the present study, we described the optimization of the catalytic oxidative bisulfite sequencing (coBS-seq), and its application to the analysis of 5hmC in genomic DNA at single base resolution in a quantitative manner. As the oxidation step showed quite low damage on genomic DNA, the method allows us to down scale the sample to be analyzed. (C) 2016 Elsevier Ltd. All rights reserved.
机译:将5-甲基胞嘧啶(5MC)的氧化由十一十一易位(TET)酶催化,以产生5-羟甲基胞嘧啶(5HMC)和后氧化产品。显示氧化核苷酸是DNA去甲基化的中间体,因为通过由胸腺嘧啶DNA糖基糖基糖酶引发的基本切除修复系统除去核苷酸。在基因组DNA中以单一基质分辨率确定初始氧化产物5HMC的简单且准确的方法是理解去甲基化机制必需的。最近,我们已经开发了使用胶束 - 被诱导的氧化剂进行新的催化氧化反应,以氧化5HMC以形成5-甲酰胞嘧啶(5FC),随后的亚硫酸氢盐测序可以确定DNA中5HMC的位置。在本研究中,我们描述了催化氧化亚硫酸氢盐测序(COBs-SEQ)的优化,及其在单个基质分辨率下的5HMC中的应用,以定量方式。随着氧化步骤对基因组DNA的损伤表示相当低,该方法允许我们向下缩小待分析的样品。 (c)2016 Elsevier Ltd.保留所有权利。

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