Rapid identification of eels Anguilla japonica and Anguilla anguilla by polymerase chain reaction with single nucleotide polymorphism-based specific probes

被引:35
作者
Itoi, S [1 ]
Nakaya, M [1 ]
Kaneko, G [1 ]
Kondo, H [1 ]
Sezaki, K [1 ]
Watabe, S [1 ]
机构
[1] Univ Tokyo, Grad Sch Agr & Life Sci, Lab Aquat Mol Biol & Biotechnol, Tokyo 1138657, Japan
关键词
16S rRNA; Anguilla anguilla; Anguilla japonica; mitochondrial DNA; real-time PCR; TaqMan minor groove binder probe;
D O I
10.1111/j.1444-2906.2005.01102.x
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Standard molecular techniques, such as sequencing and restriction fragment length polymorphism analysis after polymerase chain reaction (PCR) amplification are relatively complicated, and species identification can take a long time when using such techniques. We established a quick method, using PCR with species-specific TaqMan Minor Groove Binder (MGB) probes based on single nucleotide polymorphism (SNP) to distinguish the two eel species Anguilla japonica and Anguilla anguilla. This method can be used in processed products. Partial sequences of the mitochondrial 16S rRNA gene were compared between A. japonica and A. anguilla to design a primer pair common to both A. japonica and A. anguilla and probes specific to A. japonica and A. anguilla. Different fluorescence intensities were produced in two PCR microtubes each containing A. japonica-and A. anguilla-specific probes for one target sample. We observed the fluorescence intensity of PCR products in microtubes under ultraviolet transillumination, with similar results to those obtained by real-time PCR. Therefore, SNP-based PCR is a powerful tool for identifying materials of processed foods from either A. japonica or A. anguilla.
引用
收藏
页码:1356 / 1364
页数:9
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