Development of mitochondrial DNA cytochrome c oxidase subunit I primer sets to construct DNA barcoding library using next-generation sequencing

被引:1
|
作者
Kurata, Seikan [1 ]
Mano, Shota [2 ]
Nakahama, Naoyuki [3 ]
Hirota, Shun K. [4 ]
Suyama, Yoshihisa [5 ]
Ito, Motomi [6 ]
机构
[1] Hokkaido Univ, Tomakomai Expt Forest, Tomakomai, Japan
[2] Akita Prefectural Univ, Fac Bioresource Sci, Akita, Japan
[3] Univ Hyogo, Inst Nat & Environm Sci, Kobe, Hyogo, Japan
[4] Osaka Metropolitan Univ, Bot Gardens, Osaka, Japan
[5] Tohoku Univ, Grad Sch Agr Sci, Sendai, Miyagi, Japan
[6] Univ Tokyo, Komaba Museum, Tokyo, Japan
关键词
biodiversity; DNA barcoding; mtDNA COI; insect; next -generation sequencing; BIODIVERSITY; BUTTERFLIES; MAFFT; AREA;
D O I
10.3897/BDJ.12.e117014
中图分类号
X176 [生物多样性保护];
学科分类号
090705 ;
摘要
Insects are one of the most diverse eukaryotic groups on the planet, with one million or more species present, including those yet undescribed. The DNA barcoding system has been developed, which has aided in the identification of cryptic species and undescribed species. The mitochondrial cytochrome c oxidase I region (mtDNA COI) has been utilised for the barcoding analysis of insect taxa. Thereafter, next -generation sequencing (NGS) technology has been developed, allowing for rapid acquisition of massive amounts of sequence data for genetic analyses. Although NGS-based PCR primers designed to amplify the mtDNA COI region have been developed, their target regions were only a part of COI region and/or there were taxonomic bias for PCR amplification. As the mtDNA COI region is a traditional DNA marker for the DNA barcoding system, modified primers for this region would greatly contribute to taxonomic studies. In this study, we redesigned previously developed PCR primer sets that targetted the mtDNA COI barcoding region to improve amplification efficiency and to enable us to conduct sequencing analysis on NGS. As a result, the redesigned primer sets achieved a high success rate (> 85%) for species examined in this study, covering four insect orders (Coleoptera, Lepidoptera, Orthoptera and Odonata). Thus, by combining the primers with developed primer sets for 12S or 16S rRNA regions, we can conduct more detailed taxonomic, phylogeographic and conservation genetic studies using NGS.
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页数:20
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