McKernan Kevin J, Spangler Jessica, Zhang Lei, Tadigotla Vasisht, McLaughlin Stephen, Warner Jason, Zare Amir, Boles Richard G
Courtagen Life Sciences, Woburn, Massachusetts, United States of America.
PLoS One. 2014 May 2;9(5):e96492. doi: 10.1371/journal.pone.0096492. eCollection 2014.
We have developed a PCR method, coined Déjà vu PCR, that utilizes six nucleotides in PCR with two methyl specific restriction enzymes that respectively digest these additional nucleotides. Use of this enzyme-and-nucleotide combination enables what we term a "DNA diode", where DNA can advance in a laboratory in only one direction and cannot feedback into upstream assays. Here we describe aspects of this method that enable consecutive amplification with the introduction of a 5th and 6th base while simultaneously providing methylation dependent mitochondrial DNA enrichment. These additional nucleotides enable a novel DNA decontamination technique that generates ephemeral and easy to decontaminate DNA.
我们开发了一种名为“似曾相识PCR”的PCR方法,该方法在PCR中使用六个核苷酸,并结合两种甲基特异性限制酶,这两种酶分别消化这些额外的核苷酸。使用这种酶和核苷酸组合可实现我们所称的“DNA二极管”,即DNA在实验室中只能单向前进,无法反馈到上游检测中。在此,我们描述了该方法的一些方面,这些方面能够在引入第五和第六个碱基的同时实现连续扩增,同时提供甲基化依赖性线粒体DNA富集。这些额外的核苷酸实现了一种新型的DNA净化技术,该技术可生成短暂且易于净化的DNA。