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基于T4 DNA连接酶和反向分子信标的RNA模板单碱基突变检测

RNA-templated single-base mutation detection based on T4 DNA ligase and reverse molecular beacon.

作者信息

Tang Hongxing, Yang Xiaohai, Wang Kemin, Tan Weihong, Li Huimin, He Lifang, Liu Bin

机构信息

Engineering Center for Biomedicine, State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, PR China.

出版信息

Talanta. 2008 Jun 15;75(5):1388-93. doi: 10.1016/j.talanta.2008.01.051. Epub 2008 Feb 3.

Abstract

A novel RNA-templated single-base mutation detection method based on T4 DNA ligase and reverse molecular beacon (rMB) has been developed and successfully applied to identification of single-base mutation in codon 273 of the p53 gene. The discrimination was carried out using allele-specific primers, which flanked the variable position in the target RNA and was ligated using T4 DNA ligase only when the primers perfectly matched the RNA template. The allele-specific primers also carried complementary stem structures with end-labels (fluorophore TAMRA, quencher DABCYL), which formed a molecular beacon after RNase H digestion. One-base mismatch can be discriminated by analyzing the change of fluorescence intensity before and after RNase H digestion. This method has several advantages for practical applications, such as direct discrimination of single-base mismatch of the RNA extracted from cell; no requirement of PCR amplification; performance of homogeneous detection; and easily design of detection probes.

摘要

一种基于T4 DNA连接酶和反向分子信标(rMB)的新型RNA模板单碱基突变检测方法已被开发出来,并成功应用于p53基因第273密码子单碱基突变的鉴定。使用等位基因特异性引物进行区分,这些引物位于目标RNA的可变位置两侧,只有当引物与RNA模板完美匹配时,才会使用T4 DNA连接酶进行连接。等位基因特异性引物还带有带有末端标签(荧光团TAMRA,猝灭剂DABCYL)的互补茎结构,在RNase H消化后形成分子信标。通过分析RNase H消化前后荧光强度的变化,可以区分单碱基错配。该方法在实际应用中有几个优点,例如直接区分从细胞中提取的RNA的单碱基错配;无需PCR扩增;进行均相检测;以及检测探针易于设计。

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