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通过聚合酶链反应直接检测5-甲基胞嘧啶

Direct sensing of 5-methylcytosine by polymerase chain reaction.

作者信息

Aschenbrenner Joos, Drum Matthias, Topal Hüsnü, Wieland Markus, Marx Andreas

机构信息

Department of Chemistry, Konstanz Research School Chemical Biology, University of Konstanz, Universitätsstrasse 10, 78457 Konstanz (Germany).

出版信息

Angew Chem Int Ed Engl. 2014 Jul 28;53(31):8154-8. doi: 10.1002/anie.201403745. Epub 2014 Jun 12.

Abstract

The epigenetic control of genes by the methylation of cytosine resulting in 5-methylcytosine (5mC) has fundamental implications for human development and disease. Analysis of alterations in DNA methylation patterns is an emerging tool for cancer diagnostics and prognostics. Here we report that two thermostable DNA polymerases, namely the DNA polymerase KlenTaq derived from Thermus aquaticus and the KOD DNA polymerase from Thermococcus kodakaraensis, are able to extend 3'-mismatched primer strands more efficiently from 5 mC than from unmethylated C. This feature was advanced by generating a DNA polymerase mutant with further improved 5mC/C discrimination properties and its successful application in a novel methylation-specific PCR approach directly from untreated human genomic DNA.

摘要

胞嘧啶甲基化形成5-甲基胞嘧啶(5mC)从而对基因进行表观遗传控制,这对人类发育和疾病具有重要意义。分析DNA甲基化模式的改变是一种新兴的癌症诊断和预后工具。在此我们报告,两种热稳定DNA聚合酶,即源自嗜热栖热菌的DNA聚合酶KlenTaq和源自柯达嗜热栖热球菌的KOD DNA聚合酶,能够从5mC比从未甲基化的C更有效地延伸3' 错配引物链。通过生成具有进一步改善的5mC/C区分特性的DNA聚合酶突变体及其在直接从未经处理的人类基因组DNA进行的新型甲基化特异性PCR方法中的成功应用,这一特性得到了进一步提升。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ce0/4499253/5028765d4183/anie0053-8154-f1.jpg

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