Research Group Genetic Alterations in Carcinogenesis, German Cancer Research Center (DKFZ, Deutsches Krebsforschungszentrum), Heidelberg, Germany.
Electrophoresis. 2010 Oct;31(21):3548-51. doi: 10.1002/elps.201000357.
2'-Deoxy-N(6)-methyladenosine (N(6)mdA) is frequently found in prokaryotic and unicellular eukaryotic genomes. Although methylated bases represent only a minor fraction of the genome, they, however, exhibit strong biological effects. Here, we report a fast and sensitive method for the quantification of global adenine methylation in DNA. The method is based on a recently developed procedure consisting of fluorescence labeling of deoxyribonucleotides with BODIPY FL EDA and analysis by CE with LIF. An oligodeoxyribonucleotide site specifically modified with N(6)mdA was used for peak assignment, to establish separation conditions and to determine the LOD. The method yielded a LOD for N(6)mdA of 280 pM (1.4 amol), which is equivalent to ∼1 N(6)mdA per 10(4) normal nucleotides (0.01%) using 1 μg of DNA as the matrix. After calibration with completely dam methylated λ DNA, the assay was applied to the analysis of various DNAs.
2'-脱氧-N(6)-甲基腺苷(N(6)mdA)经常存在于原核生物和单细胞真核生物的基因组中。尽管甲基化碱基仅占基因组的一小部分,但它们却表现出强烈的生物学效应。在这里,我们报告了一种快速灵敏的定量检测 DNA 中腺嘌呤甲基化的方法。该方法基于一种新开发的方法,该方法使用 BODIPY FL EDA 荧光标记脱氧核苷酸,并通过 CE 与 LIF 进行分析。使用经 N(6)mdA 特异性修饰的寡脱氧核苷酸进行峰分配,以建立分离条件并确定检测限。该方法对 N(6)mdA 的检测限为 280 pM(1.4 amol),这相当于使用 1 μg DNA 作为基质时每个 104 个正常核苷酸中约有 1 个 N(6)mdA(0.01%)。用完全 dam 甲基化的 λ DNA 进行校准后,该测定法被应用于各种 DNA 的分析。