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Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding

DNA barcoding should provide rapid, accurate and automatable species identifications by using a standardized DNA region as a tag. Based on sequences available in GenBank and sequences produced for this study, we evaluated the resolution power of the whole chloroplast trnL (UAA) intron (254–767 bp) a...

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Autores principales: Taberlet, Pierre, Coissac, Eric, Pompanon, François, Gielly, Ludovic, Miquel, Christian, Valentini, Alice, Vermat, Thierry, Corthier, Gérard, Brochmann, Christian, Willerslev, Eske
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1807943/
https://www.ncbi.nlm.nih.gov/pubmed/17169982
http://dx.doi.org/10.1093/nar/gkl938
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author Taberlet, Pierre
Coissac, Eric
Pompanon, François
Gielly, Ludovic
Miquel, Christian
Valentini, Alice
Vermat, Thierry
Corthier, Gérard
Brochmann, Christian
Willerslev, Eske
author_facet Taberlet, Pierre
Coissac, Eric
Pompanon, François
Gielly, Ludovic
Miquel, Christian
Valentini, Alice
Vermat, Thierry
Corthier, Gérard
Brochmann, Christian
Willerslev, Eske
author_sort Taberlet, Pierre
collection PubMed
description DNA barcoding should provide rapid, accurate and automatable species identifications by using a standardized DNA region as a tag. Based on sequences available in GenBank and sequences produced for this study, we evaluated the resolution power of the whole chloroplast trnL (UAA) intron (254–767 bp) and of a shorter fragment of this intron (the P6 loop, 10–143 bp) amplified with highly conserved primers. The main limitation of the whole trnL intron for DNA barcoding remains its relatively low resolution (67.3% of the species from GenBank unambiguously identified). The resolution of the P6 loop is lower (19.5% identified) but remains higher than those of existing alternative systems. The resolution is much higher in specific contexts such as species originating from a single ecosystem, or commonly eaten plants. Despite the relatively low resolution, the whole trnL intron and its P6 loop have many advantages: the primers are highly conserved, and the amplification system is very robust. The P6 loop can even be amplified when using highly degraded DNA from processed food or from permafrost samples, and has the potential to be extensively used in food industry, in forensic science, in diet analyses based on feces and in ancient DNA studies.
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spelling pubmed-18079432007-03-02 Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding Taberlet, Pierre Coissac, Eric Pompanon, François Gielly, Ludovic Miquel, Christian Valentini, Alice Vermat, Thierry Corthier, Gérard Brochmann, Christian Willerslev, Eske Nucleic Acids Res Methods Online DNA barcoding should provide rapid, accurate and automatable species identifications by using a standardized DNA region as a tag. Based on sequences available in GenBank and sequences produced for this study, we evaluated the resolution power of the whole chloroplast trnL (UAA) intron (254–767 bp) and of a shorter fragment of this intron (the P6 loop, 10–143 bp) amplified with highly conserved primers. The main limitation of the whole trnL intron for DNA barcoding remains its relatively low resolution (67.3% of the species from GenBank unambiguously identified). The resolution of the P6 loop is lower (19.5% identified) but remains higher than those of existing alternative systems. The resolution is much higher in specific contexts such as species originating from a single ecosystem, or commonly eaten plants. Despite the relatively low resolution, the whole trnL intron and its P6 loop have many advantages: the primers are highly conserved, and the amplification system is very robust. The P6 loop can even be amplified when using highly degraded DNA from processed food or from permafrost samples, and has the potential to be extensively used in food industry, in forensic science, in diet analyses based on feces and in ancient DNA studies. Oxford University Press 2007-02 2006-12-14 /pmc/articles/PMC1807943/ /pubmed/17169982 http://dx.doi.org/10.1093/nar/gkl938 Text en © 2006 The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Online
Taberlet, Pierre
Coissac, Eric
Pompanon, François
Gielly, Ludovic
Miquel, Christian
Valentini, Alice
Vermat, Thierry
Corthier, Gérard
Brochmann, Christian
Willerslev, Eske
Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding
title Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding
title_full Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding
title_fullStr Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding
title_full_unstemmed Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding
title_short Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding
title_sort power and limitations of the chloroplast trnl (uaa) intron for plant dna barcoding
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1807943/
https://www.ncbi.nlm.nih.gov/pubmed/17169982
http://dx.doi.org/10.1093/nar/gkl938
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