A DNA barcode for land plants

作者:Hollingsworth P M*; Forrest L L; Spouge J L; Hajibabaei M; Ratnasingham S; Van Der Bank M; Chase M W; Cowan R S; Erickson D L; Fazekas A J; Graham S W; James K E; Kim K J; Kress W J; Schneider H; Van AlphenStahl J; Barrett S C H; Van Den Berg C; Bogarin D; Burgess K S; Cameron K M; Carine M; Chacon J; Clark A; Clarkson J J; Conrad F; Devey D S; Ford C S; Hedderson T A J; Hollingsworth M L; Husband B C; Kelly L J; Kesanakurti P R; Jung S K; Kim Y D; Lahaye R
来源:Proceedings of the National Academy of Sciences of USA, 2009, 106(31): 12794-12797.
DOI:10.1073/pnas.0905845106

摘要

DNA barcoding involves sequencing a standard region of DNA as a tool for species identification. However, there has been no agreement on which region(s) should be used for barcoding land plants. To provide a community recommendation on a standard plant barcode, we have compared the performance of 7 leading candidate plastid DNA regions (atpF-atpH spacer, matK gene, rbcL gene, rpoB gene, rpoC1 gene, psbK-psbI spacer, and trnH-psbA spacer). Based on assessments of recoverability, sequence quality, and levels of species discrimination, we recommend the 2-locus combination of rbcL+matK as the plant barcode. This core 2-locus barcode will provide a universal framework for the routine use of DNA sequence data to identify specimens and contribute toward the discovery of overlooked species of land plants.

  • 单位
    University of Wisconsin; new; United States; Universidad de los Andes; bpotest; university of Toronto; National Institutes of Health; Smithsonian Institution; 1; 6; university of guelph; 5; 2

全文