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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...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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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. |
format | Text |
id | pubmed-2270266 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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