首页> 外文期刊>Nucleic Acids Research >A novel procedure for simple and efficient genotyping of single nucleotide polymorphisms by using the Zn2+-cyclen complex - art. no. e126
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A novel procedure for simple and efficient genotyping of single nucleotide polymorphisms by using the Zn2+-cyclen complex - art. no. e126

机译:利用Zn2 +-细胞周期复合物简单有效地对单核苷酸多态性进行基因分型的新方法-art。没有。 e126

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摘要

The analysis of single nucleotide polymorphisms (SNPs) is increasingly utilized in the study of various genetic determinants. Here, we introduce a simple, rapid, low-cost and accurate procedure for the detection of SNPs by polyacrylamide gel electrophoresis (PAGE) with a novel additive, the Zn2+- cyclen complex (cyclen = 1,4,7,10-tetraazacyclododecane). The method is based on the difference in mobility of mutant DNA (in the same length) in PAGE, which is due to Zn2+-cyclen binding to thymine bases accompanying a total charge decrease and a local conformation change of target DNA. Various nucleotide substitutions (e.g. AT to GC) in DNA fragments (up to 150 bp) can be visualized with ethidium bromide staining. Furthermore, heteroduplex and homoduplex DNAs are clearly separated as different bands in the gel. We demonstrate the analysis of single- and multiple-nucleotide substitutions in a voltage-dependent sodium channel gene by using this novel procedure (Zn2+-cyclen-PAGE).
机译:单核苷酸多态性(SNPs)的分析越来越多地用于各种遗传决定因素的研究。在这里,我们介绍了一种简单,快速,低成本和准确的方法,用于通过聚丙烯酰胺凝胶电泳(PAGE)和新型添加剂Zn2 + -cycln络合物(cycln = 1,4,7,10-四氮杂十二烷)来检测SNP。 。该方法基于PAGE中突变DNA(相同长度)的迁移率差异,这是由于Zn2 +-环素与胸腺嘧啶碱基的结合,伴随着总电荷的减少和目标DNA的局部构象变化。 DNA片段(最高达150 bp)中的各种核苷酸取代(例如AT到GC)可以通过溴化乙锭染色进行观察。此外,异源双链和同源双链DNA在凝胶中清楚地分隔为不同的条带。我们证明了通过使用这种新颖的程序(Zn2 + -cycln-PAGE)分析电压依赖性钠通道基因中的单核苷酸和多核苷酸取代。

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