DNA barcodes from four loci provide poor resolution of taxonomic groups in the genus Crataegus.

AoB Plants

Green Plant Herbarium, Department of Natural History, Royal Ontario Museum, 100 Queen's Park, Toronto, ON, Canada M5S 2C6 Department of Ecology and Evolutionary Biology, University of Toronto, 25 Willcocks Street, Toronto, ON, Canada M5S 3B2

Published: April 2015

AI Article Synopsis

  • DNA barcodes can help identify organisms when physical traits are hard to observe, but their effectiveness in plant species identification is still unclear.
  • Research showed that four common DNA barcodes struggled to accurately differentiate hawthorn species, partly due to low resolution from individual plastid markers and complications from hybridization.
  • Concatenating multiple plastid sequences improved identification, but inconsistencies between the plastid and nuclear DNA trees highlight the challenges posed by hybridization and incomplete evolutionary processes.

Article Abstract

DNA barcodes can facilitate identification of organisms especially when morphological characters are limited or unobservable. To what extent this potential is realized in specific groups of plants remains to be determined. Libraries of barcode sequences from well-studied authoritatively identified plants represented by herbarium voucher specimens are needed in order for DNA barcodes to serve their intended purpose, where this is possible, and to understand the reasons behind their failure to do so, when this occurs. We evaluated four loci, widely regarded as universal DNA barcodes for plants, for their utility in hawthorn species identification. Three plastid regions, matK, rbcLa and psbA-trnH, and the internal transcribed spacer 2 (ITS2) of nuclear ribosomal DNA discriminate only some of the species of Crataegus that can be recognized on the basis of their morphology etc. This is, in part, because in Rosaceae tribe Maleae most individual plastid loci yield relatively little taxonomic resolution and, in part, because the effects of allopolyploidization have not been eliminated by concerted evolution of the ITS regions. Although individual plastid markers provided generally poor resolution of taxonomic groups in Crataegus, a few species were notable exceptions. In contrast, analyses of concatenated sequences of the 3 plastid barcode loci plus 11 additional plastid loci gave a well-resolved maternal phylogeny. In the ITS2 tree, different individuals of some species formed groups with taxonomically unrelated species. This is a sign of lineage sorting due to incomplete concerted evolution in ITS2. Incongruence between the ITS2 and plastid trees is best explained by hybridization between different lineages within the genus. In aggregate, limited between-species variation in plastid loci, hybridization and a lack of concerted evolution in ITS2 all combine to limit the utility of standard barcoding markers in Crataegus. These results have implications for authentication of hawthorn materials in natural health products.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4480070PMC
http://dx.doi.org/10.1093/aobpla/plv045DOI Listing

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