首页> 外文期刊>Nucleic Acids Research >Rolling-circle amplification under topological constraints
【24h】

Rolling-circle amplification under topological constraints

机译:拓扑约束下的滚圆放大

获取原文
获取原文并翻译 | 示例
           

摘要

We have performed rolling-circle amplification (RCA) reactions on three DNA templates that differ distinctly in their topology: an unlinked DNA circle, a linked DNA circle within a pseudorotaxane-type structure and a linked DNA circle within a catenane. In the linked templates, the single-stranded circle (dubbed earring probe) is threaded, with the aid of two peptide nucleic acid openers, between the two strands of double-stranded DNA (dsDNA). We have found that the RCA efficiency of amplification was essentially unaffected when the linked templates were employed. By showing that the DNA catenance remains intact after RCA reactions, we prove that certain DNA polymerases can carry out the replicative synthesis under topological constraints allowing detection of several hundred copies of a dsDNA marker without DNA denaturation. Our finding may have practical implications in the area of DNA diagnostics.
机译:我们已经对三种拓扑结构明显不同的DNA模板进行了滚环扩增(RCA)反应:未连接的DNA环,假轮烷型结构内的连接的DNA环和链烷中的连接的DNA环。在链接的模板中,借助两个肽核酸开放剂,在双链DNA(dsDNA)的两条链之间穿入单链环(配音耳环探针)。我们发现当使用链接的模板时,RCA的扩增效率基本上不受影响。通过显示RCA反应后DNA悬链保持完好无损,我们证明了某些DNA聚合酶可以在拓扑约束下进行复制合成,从而允许检测数百个dsDNA标记而无需DNA变性。我们的发现可能在DNA诊断领域具有实际意义。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号