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Towards a transferable and cost-effective plant AFLP protocol

dc.contributor.authorBlignaut, Margueriteen_ZA
dc.contributor.authorEllis, Allan G.en_ZA
dc.contributor.authorLe Roux, Johannes J.en_ZA
dc.date.accessioned2014-07-07T12:34:01Z
dc.date.available2014-07-07T12:34:01Z
dc.date.issued2013
dc.identifier.citationBlignaut, M., Ellis, A. G. & Le Roux, J. J. 2013. Towards a transferable and cost-effective plant AFLP protocol. PLoS ONE, 8(4):e61704., doi:10.1371/journal.pone.0061704.en_ZA
dc.identifier.issn1932-6203 (online)
dc.identifier.otherdoi:10.1371/journal.pone.0061704
dc.identifier.urihttp://hdl.handle.net/10019.1/94953
dc.descriptionCITATION: Blignaut, M., Ellis, A. G. & Le Roux, J. J. 2013. Towards a transferable and cost-effective plant AFLP protocol. PLoS ONE, 8(4):e61704., doi:10.1371/journal.pone.0061704.en_ZA
dc.descriptionThe original publication is available at http://journals.plos.org/plosoneen_ZA
dc.description.abstractAmplified 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.en_ZA
dc.description.urihttp://journals.plos.org/plosone/article?id=10.1371/journal.pone.0061704
dc.format.extent7 pages : illustrationsen_ZA
dc.language.isoen_ZAen_ZA
dc.publisherPLoSen_ZA
dc.subjectAmplified fragment length polymorphism (AFLP)en_ZA
dc.subjectPlant AFLP protocolen_ZA
dc.subjectPlant taxonomyen_ZA
dc.subjectEcological and population genetic studiesen_ZA
dc.titleTowards a transferable and cost-effective plant AFLP protocolen_ZA
dc.typeArticleen_ZA
dc.description.versionPublisher's versionen_ZA
dc.rights.holderAuthors retain copyrighten_ZA


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