Tang Hongxing, Yang Xiaohai, Wang Kemin, Tan Weihong, Li Huimin, He Lifang, Liu Bin
Engineering Center for Biomedicine, State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, PR China.
Talanta. 2008 Jun 15;75(5):1388-93. doi: 10.1016/j.talanta.2008.01.051. Epub 2008 Feb 3.
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.
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。