Testing four proposed barcoding markers for the identification of species within Ligustrum L. （Oleaceae）

• Published in: 植物分类学报：英文版 2011, Vol.49 (3), p.213-224
• Main Author: Jing GU jun-Xia SU Ruo-Zhu LIN Rui-Qi LI Pei-Gen XIAO
• Format: Article
• Language: English
• Subjects: matK基因; psbA基因; 分子识别能力; 女贞属; 木犀科; 条形码; 物种鉴定; 选择标记
• ISSN: 1674-4918; 1759-6831

DNA barcoding is a biological technique that uses short and standardized genes or DNA regions to facilitate species identification. DNA barcoding has been used successfully in several animal and plant groups. Ligustrum （Oleaceae） species occur widely throughout the world and are used as medicinal plants in China. Therefore, the accurate identification of species in this genus is necessary. Four potential DNA barcodes, namely the nuclear ribosomal internal transcribed spacer （ITS） and three chloroplast （cp） DNA regions （rbcL, matK, and trnH-psbA）, were used to differentiate species within Ligustrum. BLAST, character-based method, tree-based methods and TAXONDNA analysis were used to investigate the molecular identification capabilities of the chosen markers for discriminating 92 samples representing 20 species of this genus. The results showed that the ITS sequences have the most variable information, followed by trnH-psbA, matK, and rbcL. All sequences of the four regions correctly identified the species at the genus level using BLAST alignment. At the species level, the discriminating power of rbcL, marK, trnH-psbA, and ITS based on neighbor-joining （NJ） trees was 36.8%, 38.9%, 77.8%, and 80%, respectively. Using character-based and maximum parsimony （MP） tree methods together, the discriminating ability of trnH-psbA increased to 88.9%. All species could be differentiated using ITS when combining the NJ tree method with character-based or MP tree methods. Overall, the results indicate that DNA barcoding is an effective molecular identification method for Ligustrum species. We propose the nuclear ribosomal ITS as a plant barcode for plant identification and trnH-psbA as a candidate barcode sequence.