DArT for high-throughput genotyping of cassava (Manihot esculenta) and its wild relatives

Understanding the distribution of genetic diversity within and among individuals, populations, species and gene pools is crucial for the efficient management of germplasm collections. Molecular markers are playing an increasing role in germplasm characterization, yet their broad application is limit...

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Autores principales: Xia, L, Peng, K, Yang, S, Wenzl, Peter, Vicente, M. Carmen de, Fregene, Martin A., Kilian, Andrzej
Formato: Journal Article
Lenguaje:Inglés
Publicado: Springer 2005
Materias:
Acceso en línea:https://hdl.handle.net/10568/42715
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author Xia, L
Peng, K
Yang, S
Wenzl, Peter
Vicente, M. Carmen de
Fregene, Martin A.
Kilian, Andrzej
author_browse Fregene, Martin A.
Kilian, Andrzej
Peng, K
Vicente, M. Carmen de
Wenzl, Peter
Xia, L
Yang, S
author_facet Xia, L
Peng, K
Yang, S
Wenzl, Peter
Vicente, M. Carmen de
Fregene, Martin A.
Kilian, Andrzej
author_sort Xia, L
collection Repository of Agricultural Research Outputs (CGSpace)
description Understanding the distribution of genetic diversity within and among individuals, populations, species and gene pools is crucial for the efficient management of germplasm collections. Molecular markers are playing an increasing role in germplasm characterization, yet their broad application is limited by the availability of markers, the costs and the low throughput of existing technologies. This is particularly true for crops of resource-poor farmers such as cassava, Manihot esculenta. Here we report on the development of Diversity Arrays Technology (DArT) for cassava. DArT uses microarrays to detect DNA polymorphism at several hundred genomic loci in a single assay without relying on DNA sequence information. We tested three complexity reduction methods and selected the two that generated genomic representations with the largest frequency of polymorphic clones (PstI/TaqI: 14.6%, PstI/BstNI: 17.2%) to produce large genotyping arrays. Nearly 1,000 candidate polymorphic clones were detected on the two arrays. The performance of the PstI/TaqI array was validated by typing a group of 38 accessions, 24 of them in duplicate. The average call rate was 98.1%, and the scoring reproducibility was 99.8%. DArT markers displayed fairly high polymorphism information content (PIC) values and revealed genetic relationships among the samples consistent with the information available on these samples. Our study suggests that DArT offers advantages over current technologies in terms of cost and speed of marker discovery and analysis. It can therefore be used to genotype large germplasm collections.
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spelling CGSpace427152024-08-27T10:35:06Z DArT for high-throughput genotyping of cassava (Manihot esculenta) and its wild relatives Xia, L Peng, K Yang, S Wenzl, Peter Vicente, M. Carmen de Fregene, Martin A. Kilian, Andrzej manihot esculenta plant breeding germplasm collections methods evaluation genotypes genetic variation genetic polymorphism fitomejoramiento colecciones de material genético métodos evaluación genotipos variación genética polimorfismo genético genetics biotechnology Understanding the distribution of genetic diversity within and among individuals, populations, species and gene pools is crucial for the efficient management of germplasm collections. Molecular markers are playing an increasing role in germplasm characterization, yet their broad application is limited by the availability of markers, the costs and the low throughput of existing technologies. This is particularly true for crops of resource-poor farmers such as cassava, Manihot esculenta. Here we report on the development of Diversity Arrays Technology (DArT) for cassava. DArT uses microarrays to detect DNA polymorphism at several hundred genomic loci in a single assay without relying on DNA sequence information. We tested three complexity reduction methods and selected the two that generated genomic representations with the largest frequency of polymorphic clones (PstI/TaqI: 14.6%, PstI/BstNI: 17.2%) to produce large genotyping arrays. Nearly 1,000 candidate polymorphic clones were detected on the two arrays. The performance of the PstI/TaqI array was validated by typing a group of 38 accessions, 24 of them in duplicate. The average call rate was 98.1%, and the scoring reproducibility was 99.8%. DArT markers displayed fairly high polymorphism information content (PIC) values and revealed genetic relationships among the samples consistent with the information available on these samples. Our study suggests that DArT offers advantages over current technologies in terms of cost and speed of marker discovery and analysis. It can therefore be used to genotype large germplasm collections. 2005-04 2014-09-24T07:58:27Z 2014-09-24T07:58:27Z Journal Article https://hdl.handle.net/10568/42715 en Limited Access Springer
spellingShingle manihot esculenta
plant breeding
germplasm collections
methods
evaluation
genotypes
genetic variation
genetic polymorphism
fitomejoramiento
colecciones de material genético
métodos
evaluación
genotipos
variación genética
polimorfismo genético
genetics
biotechnology
Xia, L
Peng, K
Yang, S
Wenzl, Peter
Vicente, M. Carmen de
Fregene, Martin A.
Kilian, Andrzej
DArT for high-throughput genotyping of cassava (Manihot esculenta) and its wild relatives
title DArT for high-throughput genotyping of cassava (Manihot esculenta) and its wild relatives
title_full DArT for high-throughput genotyping of cassava (Manihot esculenta) and its wild relatives
title_fullStr DArT for high-throughput genotyping of cassava (Manihot esculenta) and its wild relatives
title_full_unstemmed DArT for high-throughput genotyping of cassava (Manihot esculenta) and its wild relatives
title_short DArT for high-throughput genotyping of cassava (Manihot esculenta) and its wild relatives
title_sort dart for high throughput genotyping of cassava manihot esculenta and its wild relatives
topic manihot esculenta
plant breeding
germplasm collections
methods
evaluation
genotypes
genetic variation
genetic polymorphism
fitomejoramiento
colecciones de material genético
métodos
evaluación
genotipos
variación genética
polimorfismo genético
genetics
biotechnology
url https://hdl.handle.net/10568/42715
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