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A platform for efficient genotyping in Musa using microsatellite markers

BACKGROUND AND AIMS: Bananas and plantains (Musa spp.) are one of the major fruit crops worldwide with acknowledged importance as a staple food for millions of people. The rich genetic diversity of this crop is, however, endangered by diseases, adverse environmental conditions and changed farming pr...

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Autores principales: Christelová, Pavla, Valárik, Miroslav, Hřibová, Eva, Van den houwe, Ines, Channelière, Stéphanie, Roux, Nicolas, Doležel, Jaroslav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185971/
https://www.ncbi.nlm.nih.gov/pubmed/22476494
http://dx.doi.org/10.1093/aobpla/plr024
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author Christelová, Pavla
Valárik, Miroslav
Hřibová, Eva
Van den houwe, Ines
Channelière, Stéphanie
Roux, Nicolas
Doležel, Jaroslav
author_facet Christelová, Pavla
Valárik, Miroslav
Hřibová, Eva
Van den houwe, Ines
Channelière, Stéphanie
Roux, Nicolas
Doležel, Jaroslav
author_sort Christelová, Pavla
collection PubMed
description BACKGROUND AND AIMS: Bananas and plantains (Musa spp.) are one of the major fruit crops worldwide with acknowledged importance as a staple food for millions of people. The rich genetic diversity of this crop is, however, endangered by diseases, adverse environmental conditions and changed farming practices, and the need for its characterization and preservation is urgent. With the aim of providing a simple and robust approach for molecular characterization of Musa species, we developed an optimized genotyping platform using 19 published simple sequence repeat markers. METHODOLOGY: The genotyping system is based on 19 microsatellite loci, which are scored using fluorescently labelled primers and high-throughput capillary electrophoresis separation with high resolution. This genotyping platform was tested and optimized on a set of 70 diploid and 38 triploid banana accessions. PRINCIPAL RESULTS: The marker set used in this study provided enough polymorphism to discriminate between individual species, subspecies and subgroups of all accessions of Musa. Likewise, the capability of identifying duplicate samples was confirmed. Based on the results of a blind test, the genotyping system was confirmed to be suitable for characterization of unknown accessions. CONCLUSIONS: Here we report on the first complex and standardized platform for molecular characterization of Musa germplasm that is ready to use for the wider Musa research and breeding community. We believe that this genotyping system offers a versatile tool that can accommodate all possible requirements for characterizing Musa diversity, and is economical for samples ranging from one to many accessions.
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spelling pubmed-31859712011-10-04 A platform for efficient genotyping in Musa using microsatellite markers Christelová, Pavla Valárik, Miroslav Hřibová, Eva Van den houwe, Ines Channelière, Stéphanie Roux, Nicolas Doležel, Jaroslav AoB Plants Research Articles BACKGROUND AND AIMS: Bananas and plantains (Musa spp.) are one of the major fruit crops worldwide with acknowledged importance as a staple food for millions of people. The rich genetic diversity of this crop is, however, endangered by diseases, adverse environmental conditions and changed farming practices, and the need for its characterization and preservation is urgent. With the aim of providing a simple and robust approach for molecular characterization of Musa species, we developed an optimized genotyping platform using 19 published simple sequence repeat markers. METHODOLOGY: The genotyping system is based on 19 microsatellite loci, which are scored using fluorescently labelled primers and high-throughput capillary electrophoresis separation with high resolution. This genotyping platform was tested and optimized on a set of 70 diploid and 38 triploid banana accessions. PRINCIPAL RESULTS: The marker set used in this study provided enough polymorphism to discriminate between individual species, subspecies and subgroups of all accessions of Musa. Likewise, the capability of identifying duplicate samples was confirmed. Based on the results of a blind test, the genotyping system was confirmed to be suitable for characterization of unknown accessions. CONCLUSIONS: Here we report on the first complex and standardized platform for molecular characterization of Musa germplasm that is ready to use for the wider Musa research and breeding community. We believe that this genotyping system offers a versatile tool that can accommodate all possible requirements for characterizing Musa diversity, and is economical for samples ranging from one to many accessions. Oxford University Press 2011 2011-08-22 /pmc/articles/PMC3185971/ /pubmed/22476494 http://dx.doi.org/10.1093/aobpla/plr024 Text en Published by Oxford University Press http://creativecommons.org/licenses/by-nc/2.5/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Christelová, Pavla
Valárik, Miroslav
Hřibová, Eva
Van den houwe, Ines
Channelière, Stéphanie
Roux, Nicolas
Doležel, Jaroslav
A platform for efficient genotyping in Musa using microsatellite markers
title A platform for efficient genotyping in Musa using microsatellite markers
title_full A platform for efficient genotyping in Musa using microsatellite markers
title_fullStr A platform for efficient genotyping in Musa using microsatellite markers
title_full_unstemmed A platform for efficient genotyping in Musa using microsatellite markers
title_short A platform for efficient genotyping in Musa using microsatellite markers
title_sort platform for efficient genotyping in musa using microsatellite markers
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185971/
https://www.ncbi.nlm.nih.gov/pubmed/22476494
http://dx.doi.org/10.1093/aobpla/plr024
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