Towards a transferable and cost-effective plant AFLP protocol.

Amplified fragment length polymorphism (AFLP) is a powerful fingerprinting technique that is widely applied in ecological and population genetic studies. However, its routine use has been limited by high costs associated with the optimization of fluorescently labelled markers, especially for individ...

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Main Authors: Marguerite Blignaut, Allan G Ellis, Johannes J Le Roux
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3628351?pdf=render
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spelling doaj-d997640d3e3543a8bbd304f1d702051a2020-11-25T02:42:28ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0184e6170410.1371/journal.pone.0061704Towards a transferable and cost-effective plant AFLP protocol.Marguerite BlignautAllan G EllisJohannes J Le RouxAmplified fragment length polymorphism (AFLP) is a powerful fingerprinting technique that is widely applied in ecological and population genetic studies. However, its routine use has been limited by high costs associated with the optimization of fluorescently labelled markers, especially for individual study systems. Here we develop a low-cost AFLP protocol that can be easily transferred between distantly related plant taxa. Three fluorescently labelled EcoRI-primers with anchors that target interspecifically conserved genomic regions were used in combination with a single non-labelled primer in our AFLP protocol. The protocol was used to genotype one gymnosperm, two monocot and three eudicot plant genera representing four invasive and four native angiosperm species (Pinus pinaster (Pinaceae), Pennisetum setaceum and Poa annua (Poaceae), Lantana camara (Verbenaceae), Bassia diffusa (Chenopodiaceae), Salvia lanceolata, Salvia africana-lutea, and Salvia africana-caerulea (Lamiaceae)). Highly polymorphic and reproducible genotypic fingerprints (between 37-144 polymorphic loci per species tested) were obtained for all taxa tested. Our single protocol was easily transferred between distantly related taxa. Measures of expected heterozygosity ranged from 0.139 to 0.196 for P. annua and from 0.168 to 0.272 for L. camara which compared well with previously published reports. In addition to ease of transferability of a single AFLP protocol, our protocol reduces costs associated with commercial kits by almost half. The use of highly conserved but abundant anchor sequences reduces the need for laborious screening for usable primers that result in polymorphic fingerprints, and appears to be the main reason for ease of transferability of our protocol between distantly related taxa.http://europepmc.org/articles/PMC3628351?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Marguerite Blignaut
Allan G Ellis
Johannes J Le Roux
spellingShingle Marguerite Blignaut
Allan G Ellis
Johannes J Le Roux
Towards a transferable and cost-effective plant AFLP protocol.
PLoS ONE
author_facet Marguerite Blignaut
Allan G Ellis
Johannes J Le Roux
author_sort Marguerite Blignaut
title Towards a transferable and cost-effective plant AFLP protocol.
title_short Towards a transferable and cost-effective plant AFLP protocol.
title_full Towards a transferable and cost-effective plant AFLP protocol.
title_fullStr Towards a transferable and cost-effective plant AFLP protocol.
title_full_unstemmed Towards a transferable and cost-effective plant AFLP protocol.
title_sort towards a transferable and cost-effective plant aflp protocol.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Amplified fragment length polymorphism (AFLP) is a powerful fingerprinting technique that is widely applied in ecological and population genetic studies. However, its routine use has been limited by high costs associated with the optimization of fluorescently labelled markers, especially for individual study systems. Here we develop a low-cost AFLP protocol that can be easily transferred between distantly related plant taxa. Three fluorescently labelled EcoRI-primers with anchors that target interspecifically conserved genomic regions were used in combination with a single non-labelled primer in our AFLP protocol. The protocol was used to genotype one gymnosperm, two monocot and three eudicot plant genera representing four invasive and four native angiosperm species (Pinus pinaster (Pinaceae), Pennisetum setaceum and Poa annua (Poaceae), Lantana camara (Verbenaceae), Bassia diffusa (Chenopodiaceae), Salvia lanceolata, Salvia africana-lutea, and Salvia africana-caerulea (Lamiaceae)). Highly polymorphic and reproducible genotypic fingerprints (between 37-144 polymorphic loci per species tested) were obtained for all taxa tested. Our single protocol was easily transferred between distantly related taxa. Measures of expected heterozygosity ranged from 0.139 to 0.196 for P. annua and from 0.168 to 0.272 for L. camara which compared well with previously published reports. In addition to ease of transferability of a single AFLP protocol, our protocol reduces costs associated with commercial kits by almost half. The use of highly conserved but abundant anchor sequences reduces the need for laborious screening for usable primers that result in polymorphic fingerprints, and appears to be the main reason for ease of transferability of our protocol between distantly related taxa.
url http://europepmc.org/articles/PMC3628351?pdf=render
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AT johannesjleroux towardsatransferableandcosteffectiveplantaflpprotocol
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