Karaiskou Nikoletta, Triantafyllidis Alexander, Triantaphyllidis Costas
Department of Genetics, Development and Molecular Biology, School of Biology, Aristotle University of Thessaloniki, 54 124 Thessaloniki, Macedonia, Greece.
J Agric Food Chem. 2003 Aug 13;51(17):4935-40. doi: 10.1021/jf034063n.
A double-DNA approach was developed to discriminate the three Trachurus species that abide in European waters: T. trachurus, T. mediterraneus, and T. picturatus. The analysis aimed at both mitochondrial and nuclear loci. Polymerase Chain Reaction (PCR) amplification of the cytochrome b gene of mtDNA was followed by restriction analysis with three species-specific enzymes: NlaIII, NciI, and BsmAI. Digestion with these endonucleases yielded species-specific electrophoretic profiles. The universality of the results was verified by screening a large number of individuals from 12 geographical regions covering most of the distribution of the species. Additionally, the nuclear multicopy 5S rRNA gene was selected as an alternative candidate for the discrimination of the three Trachurusspecies. A simple agarose gel electrophoretic analysis of the amplicons proved to be capable of leading to unambiguous identification of the three Trachurus species. Thus, the double-DNA methodology presented here allows the accurate discrimination of Trachurus fish species and the detection of commercial fraud.
开发了一种双DNA方法来区分栖息在欧洲水域的三种竹荚鱼:竹荚鱼(Trachurus trachurus)、地中海竹荚鱼(T. mediterraneus)和斑纹竹荚鱼(T. picturatus)。该分析针对线粒体和核基因座。对线粒体DNA的细胞色素b基因进行聚合酶链反应(PCR)扩增,然后用三种物种特异性酶:NlaIII、NciI和BsmAI进行限制性分析。用这些内切酶消化产生物种特异性的电泳图谱。通过对来自覆盖这些物种大部分分布区域的12个地理区域的大量个体进行筛选,验证了结果的普遍性。此外,选择核多拷贝5S rRNA基因作为区分这三种竹荚鱼的替代候选基因。对扩增产物进行简单的琼脂糖凝胶电泳分析,结果证明能够明确鉴定这三种竹荚鱼。因此,本文提出的双DNA方法能够准确区分竹荚鱼种类并检测商业欺诈行为。