rbcL and matK earn two thumbs up as the core DNA barcode for ferns.

<h4>Background</h4>DNA barcoding will revolutionize our understanding of fern ecology, most especially because the accurate identification of the independent but cryptic gametophyte phase of the fern's life history--an endeavor previously impossible--will finally be feasible. In thi...

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Autores principales: Fay-Wei Li, Li-Yaung Kuo, Carl J Rothfels, Atsushi Ebihara, Wen-Liang Chiou, Michael D Windham, Kathleen M Pryer
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Publicado: Public Library of Science (PLoS) 2011
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spelling oai:doaj.org-article:b0ac8c98d7c6435aa480306ee2e76e2f2021-11-18T07:36:00ZrbcL and matK earn two thumbs up as the core DNA barcode for ferns.1932-620310.1371/journal.pone.0026597https://doaj.org/article/b0ac8c98d7c6435aa480306ee2e76e2f2011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22028918/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>DNA barcoding will revolutionize our understanding of fern ecology, most especially because the accurate identification of the independent but cryptic gametophyte phase of the fern's life history--an endeavor previously impossible--will finally be feasible. In this study, we assess the discriminatory power of the core plant DNA barcode (rbcL and matK), as well as alternatively proposed fern barcodes (trnH-psbA and trnL-F), across all major fern lineages. We also present plastid barcode data for two genera in the hyperdiverse polypod clade--Deparia (Woodsiaceae) and the Cheilanthes marginata group (currently being segregated as a new genus of Pteridaceae)--to further evaluate the resolving power of these loci.<h4>Principal findings</h4>Our results clearly demonstrate the value of matK data, previously unavailable in ferns because of difficulties in amplification due to a major rearrangement of the plastid genome. With its high sequence variation, matK complements rbcL to provide a two-locus barcode with strong resolving power. With sequence variation comparable to matK, trnL-F appears to be a suitable alternative barcode region in ferns, and perhaps should be added to the core barcode region if universal primer development for matK fails. In contrast, trnH-psbA shows dramatically reduced sequence variation for the majority of ferns. This is likely due to the translocation of this segment of the plastid genome into the inverted repeat regions, which are known to have a highly constrained substitution rate.<h4>Conclusions</h4>Our study provides the first endorsement of the two-locus barcode (rbcL+matK) in ferns, and favors trnL-F over trnH-psbA as a potential back-up locus. Future work should focus on gathering more fern matK sequence data to facilitate universal primer development.Fay-Wei LiLi-Yaung KuoCarl J RothfelsAtsushi EbiharaWen-Liang ChiouMichael D WindhamKathleen M PryerPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 10, p e26597 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Fay-Wei Li
Li-Yaung Kuo
Carl J Rothfels
Atsushi Ebihara
Wen-Liang Chiou
Michael D Windham
Kathleen M Pryer
rbcL and matK earn two thumbs up as the core DNA barcode for ferns.
description <h4>Background</h4>DNA barcoding will revolutionize our understanding of fern ecology, most especially because the accurate identification of the independent but cryptic gametophyte phase of the fern's life history--an endeavor previously impossible--will finally be feasible. In this study, we assess the discriminatory power of the core plant DNA barcode (rbcL and matK), as well as alternatively proposed fern barcodes (trnH-psbA and trnL-F), across all major fern lineages. We also present plastid barcode data for two genera in the hyperdiverse polypod clade--Deparia (Woodsiaceae) and the Cheilanthes marginata group (currently being segregated as a new genus of Pteridaceae)--to further evaluate the resolving power of these loci.<h4>Principal findings</h4>Our results clearly demonstrate the value of matK data, previously unavailable in ferns because of difficulties in amplification due to a major rearrangement of the plastid genome. With its high sequence variation, matK complements rbcL to provide a two-locus barcode with strong resolving power. With sequence variation comparable to matK, trnL-F appears to be a suitable alternative barcode region in ferns, and perhaps should be added to the core barcode region if universal primer development for matK fails. In contrast, trnH-psbA shows dramatically reduced sequence variation for the majority of ferns. This is likely due to the translocation of this segment of the plastid genome into the inverted repeat regions, which are known to have a highly constrained substitution rate.<h4>Conclusions</h4>Our study provides the first endorsement of the two-locus barcode (rbcL+matK) in ferns, and favors trnL-F over trnH-psbA as a potential back-up locus. Future work should focus on gathering more fern matK sequence data to facilitate universal primer development.
format article
author Fay-Wei Li
Li-Yaung Kuo
Carl J Rothfels
Atsushi Ebihara
Wen-Liang Chiou
Michael D Windham
Kathleen M Pryer
author_facet Fay-Wei Li
Li-Yaung Kuo
Carl J Rothfels
Atsushi Ebihara
Wen-Liang Chiou
Michael D Windham
Kathleen M Pryer
author_sort Fay-Wei Li
title rbcL and matK earn two thumbs up as the core DNA barcode for ferns.
title_short rbcL and matK earn two thumbs up as the core DNA barcode for ferns.
title_full rbcL and matK earn two thumbs up as the core DNA barcode for ferns.
title_fullStr rbcL and matK earn two thumbs up as the core DNA barcode for ferns.
title_full_unstemmed rbcL and matK earn two thumbs up as the core DNA barcode for ferns.
title_sort rbcl and matk earn two thumbs up as the core dna barcode for ferns.
publisher Public Library of Science (PLoS)
publishDate 2011
url https://doaj.org/article/b0ac8c98d7c6435aa480306ee2e76e2f
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