BMC Genomics (May 2008)

A universal DNA mini-barcode for biodiversity analysis

  • Hebert Paul DN,
  • Hickey Donal A,
  • Landry Jean-François,
  • Singer Gregory AC,
  • Meusnier Isabelle,
  • Hajibabaei Mehrdad

DOI
https://doi.org/10.1186/1471-2164-9-214
Journal volume & issue
Vol. 9, no. 1
p. 214

Abstract

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Abstract Background The goal of DNA barcoding is to develop a species-specific sequence library for all eukaryotes. A 650 bp fragment of the cytochrome c oxidase 1 (CO1) gene has been used successfully for species-level identification in several animal groups. It may be difficult in practice, however, to retrieve a 650 bp fragment from archival specimens, (because of DNA degradation) or from environmental samples (where universal primers are needed). Results We used a bioinformatics analysis using all CO1 barcode sequences from GenBank and calculated the probability of having species-specific barcodes for varied size fragments. This analysis established the potential of much smaller fragments, mini-barcodes, for identifying unknown specimens. We then developed a universal primer set for the amplification of mini-barcodes. We further successfully tested the utility of this primer set on a comprehensive set of taxa from all major eukaryotic groups as well as archival specimens. Conclusion In this study we address the important issue of minimum amount of sequence information required for identifying species in DNA barcoding. We establish a novel approach based on a much shorter barcode sequence and demonstrate its effectiveness in archival specimens. This approach will significantly broaden the application of DNA barcoding in biodiversity studies.