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The utility of DNA barcodes to confirm the identification of palm collections in botanical gardens

The palm family (Arecaceae) is of high ecological and economic value, yet identification in the family remains a challenge for both taxonomists and horticulturalists. The family consists of approximately 2600 species across 181 genera and DNA barcoding may be a useful tool for species identification...

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Autores principales: Le, Duc-Thanh, Zhang, Yu-Qu, Xu, Yong, Guo, Li-Xiu, Ruan, Zhi-Ping, Burgess, Kevin S., Ge, Xue-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394517/
https://www.ncbi.nlm.nih.gov/pubmed/32735584
http://dx.doi.org/10.1371/journal.pone.0235569
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author Le, Duc-Thanh
Zhang, Yu-Qu
Xu, Yong
Guo, Li-Xiu
Ruan, Zhi-Ping
Burgess, Kevin S.
Ge, Xue-Jun
author_facet Le, Duc-Thanh
Zhang, Yu-Qu
Xu, Yong
Guo, Li-Xiu
Ruan, Zhi-Ping
Burgess, Kevin S.
Ge, Xue-Jun
author_sort Le, Duc-Thanh
collection PubMed
description The palm family (Arecaceae) is of high ecological and economic value, yet identification in the family remains a challenge for both taxonomists and horticulturalists. The family consists of approximately 2600 species across 181 genera and DNA barcoding may be a useful tool for species identification within the group. However, there have been few systematic evaluations of DNA barcodes for the palm family. In the present study, five DNA barcodes (rbcL, matK, trnH-psbA, ITS, ITS2) were evaluated for species identification ability across 669 samples representing 314 species and 100 genera in the Arecaceae, employing four analytical methods. The ITS gene region was found to not be a suitable barcode for the palm family, due in part, to low recovery rates and paralogous gene copies. Among the four analyses used, species resolution for ITS2 was much higher than that achieved with the plastid barcodes alone (rbcL, matK, trnH-psbA), and the barcode combination ITS2 + matK + rbcL gave the highest resolution among all single barcodes and their combinations, followed by ITS2 + matK. Among 669 palm samples analyzed, 110 samples (16.3%) were found to be misidentified. The 2992 DNA barcode sequences generated in this study greatly enriches the existing identification toolbox available to plant taxonomists that are interested in researching genetic relationships among palm taxa as well as for horticulturalists that need to confirm palm collections for botanical garden curation and horticultural applications. Our results indicate that the use of the ITS2 DNA barcode gene region provides a useful and cost-effective tool to confirm the identity of taxa in the Palm family.
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spelling pubmed-73945172020-08-07 The utility of DNA barcodes to confirm the identification of palm collections in botanical gardens Le, Duc-Thanh Zhang, Yu-Qu Xu, Yong Guo, Li-Xiu Ruan, Zhi-Ping Burgess, Kevin S. Ge, Xue-Jun PLoS One Research Article The palm family (Arecaceae) is of high ecological and economic value, yet identification in the family remains a challenge for both taxonomists and horticulturalists. The family consists of approximately 2600 species across 181 genera and DNA barcoding may be a useful tool for species identification within the group. However, there have been few systematic evaluations of DNA barcodes for the palm family. In the present study, five DNA barcodes (rbcL, matK, trnH-psbA, ITS, ITS2) were evaluated for species identification ability across 669 samples representing 314 species and 100 genera in the Arecaceae, employing four analytical methods. The ITS gene region was found to not be a suitable barcode for the palm family, due in part, to low recovery rates and paralogous gene copies. Among the four analyses used, species resolution for ITS2 was much higher than that achieved with the plastid barcodes alone (rbcL, matK, trnH-psbA), and the barcode combination ITS2 + matK + rbcL gave the highest resolution among all single barcodes and their combinations, followed by ITS2 + matK. Among 669 palm samples analyzed, 110 samples (16.3%) were found to be misidentified. The 2992 DNA barcode sequences generated in this study greatly enriches the existing identification toolbox available to plant taxonomists that are interested in researching genetic relationships among palm taxa as well as for horticulturalists that need to confirm palm collections for botanical garden curation and horticultural applications. Our results indicate that the use of the ITS2 DNA barcode gene region provides a useful and cost-effective tool to confirm the identity of taxa in the Palm family. Public Library of Science 2020-07-31 /pmc/articles/PMC7394517/ /pubmed/32735584 http://dx.doi.org/10.1371/journal.pone.0235569 Text en © 2020 Le et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Le, Duc-Thanh
Zhang, Yu-Qu
Xu, Yong
Guo, Li-Xiu
Ruan, Zhi-Ping
Burgess, Kevin S.
Ge, Xue-Jun
The utility of DNA barcodes to confirm the identification of palm collections in botanical gardens
title The utility of DNA barcodes to confirm the identification of palm collections in botanical gardens
title_full The utility of DNA barcodes to confirm the identification of palm collections in botanical gardens
title_fullStr The utility of DNA barcodes to confirm the identification of palm collections in botanical gardens
title_full_unstemmed The utility of DNA barcodes to confirm the identification of palm collections in botanical gardens
title_short The utility of DNA barcodes to confirm the identification of palm collections in botanical gardens
title_sort utility of dna barcodes to confirm the identification of palm collections in botanical gardens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394517/
https://www.ncbi.nlm.nih.gov/pubmed/32735584
http://dx.doi.org/10.1371/journal.pone.0235569
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