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DArT markers: diversity analyses and mapping in Sorghum bicolor

BACKGROUND: The sequential nature of gel-based marker systems entails low throughput and high costs per assay. Commonly used marker systems such as SSR and SNP are also dependent on sequence information. These limitations result in high cost per data point and significantly limit the capacity of bre...

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Autores principales: Mace, Emma S, Xia, Ling, Jordan, David R, Halloran, Kirsten, Parh, Dipal K, Huttner, Eric, Wenzl, Peter, Kilian, Andrzej
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2270266/
https://www.ncbi.nlm.nih.gov/pubmed/18208620
http://dx.doi.org/10.1186/1471-2164-9-26
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author Mace, Emma S
Xia, Ling
Jordan, David R
Halloran, Kirsten
Parh, Dipal K
Huttner, Eric
Wenzl, Peter
Kilian, Andrzej
author_facet Mace, Emma S
Xia, Ling
Jordan, David R
Halloran, Kirsten
Parh, Dipal K
Huttner, Eric
Wenzl, Peter
Kilian, Andrzej
author_sort Mace, Emma S
collection PubMed
description BACKGROUND: The sequential nature of gel-based marker systems entails low throughput and high costs per assay. Commonly used marker systems such as SSR and SNP are also dependent on sequence information. These limitations result in high cost per data point and significantly limit the capacity of breeding programs to obtain sufficient return on investment to justify the routine use of marker-assisted breeding for many traits and particularly quantitative traits. Diversity Arrays Technology (DArT™) is a cost effective hybridisation-based marker technology that offers a high multiplexing level while being independent of sequence information. This technology offers sorghum breeding programs an alternative approach to whole-genome profiling. We report on the development, application, mapping and utility of DArT™ markers for sorghum germplasm. RESULTS: A genotyping array was developed representing approximately 12,000 genomic clones using PstI+BanII complexity with a subset of clones obtained through the suppression subtractive hybridisation (SSH) method. The genotyping array was used to analyse a diverse set of sorghum genotypes and screening a Recombinant Inbred Lines (RIL) mapping population. Over 500 markers detected variation among 90 accessions used in a diversity analysis. Cluster analysis discriminated well between all 90 genotypes. To confirm that the sorghum DArT markers behave in a Mendelian manner, we constructed a genetic linkage map for a cross between R931945-2-2 and IS 8525 integrating DArT and other marker types. In total, 596 markers could be placed on the integrated linkage map, which spanned 1431.6 cM. The genetic linkage map had an average marker density of 1/2.39 cM, with an average DArT marker density of 1/3.9 cM. CONCLUSION: We have successfully developed DArT markers for Sorghum bicolor and have demonstrated that DArT provides high quality markers that can be used for diversity analyses and to construct medium-density genetic linkage maps. The high number of DArT markers generated in a single assay not only provides a precise estimate of genetic relationships among genotypes, but also their even distribution over the genome offers real advantages for a range of molecular breeding and genomics applications.
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spelling pubmed-22702662008-03-20 DArT markers: diversity analyses and mapping in Sorghum bicolor Mace, Emma S Xia, Ling Jordan, David R Halloran, Kirsten Parh, Dipal K Huttner, Eric Wenzl, Peter Kilian, Andrzej BMC Genomics Research Article BACKGROUND: The sequential nature of gel-based marker systems entails low throughput and high costs per assay. Commonly used marker systems such as SSR and SNP are also dependent on sequence information. These limitations result in high cost per data point and significantly limit the capacity of breeding programs to obtain sufficient return on investment to justify the routine use of marker-assisted breeding for many traits and particularly quantitative traits. Diversity Arrays Technology (DArT™) is a cost effective hybridisation-based marker technology that offers a high multiplexing level while being independent of sequence information. This technology offers sorghum breeding programs an alternative approach to whole-genome profiling. We report on the development, application, mapping and utility of DArT™ markers for sorghum germplasm. RESULTS: A genotyping array was developed representing approximately 12,000 genomic clones using PstI+BanII complexity with a subset of clones obtained through the suppression subtractive hybridisation (SSH) method. The genotyping array was used to analyse a diverse set of sorghum genotypes and screening a Recombinant Inbred Lines (RIL) mapping population. Over 500 markers detected variation among 90 accessions used in a diversity analysis. Cluster analysis discriminated well between all 90 genotypes. To confirm that the sorghum DArT markers behave in a Mendelian manner, we constructed a genetic linkage map for a cross between R931945-2-2 and IS 8525 integrating DArT and other marker types. In total, 596 markers could be placed on the integrated linkage map, which spanned 1431.6 cM. The genetic linkage map had an average marker density of 1/2.39 cM, with an average DArT marker density of 1/3.9 cM. CONCLUSION: We have successfully developed DArT markers for Sorghum bicolor and have demonstrated that DArT provides high quality markers that can be used for diversity analyses and to construct medium-density genetic linkage maps. The high number of DArT markers generated in a single assay not only provides a precise estimate of genetic relationships among genotypes, but also their even distribution over the genome offers real advantages for a range of molecular breeding and genomics applications. BioMed Central 2008-01-22 /pmc/articles/PMC2270266/ /pubmed/18208620 http://dx.doi.org/10.1186/1471-2164-9-26 Text en Copyright © 2008 Mace et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mace, Emma S
Xia, Ling
Jordan, David R
Halloran, Kirsten
Parh, Dipal K
Huttner, Eric
Wenzl, Peter
Kilian, Andrzej
DArT markers: diversity analyses and mapping in Sorghum bicolor
title DArT markers: diversity analyses and mapping in Sorghum bicolor
title_full DArT markers: diversity analyses and mapping in Sorghum bicolor
title_fullStr DArT markers: diversity analyses and mapping in Sorghum bicolor
title_full_unstemmed DArT markers: diversity analyses and mapping in Sorghum bicolor
title_short DArT markers: diversity analyses and mapping in Sorghum bicolor
title_sort dart markers: diversity analyses and mapping in sorghum bicolor
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2270266/
https://www.ncbi.nlm.nih.gov/pubmed/18208620
http://dx.doi.org/10.1186/1471-2164-9-26
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