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Development and mapping of DArT markers within the Festuca - Lolium complex
BMC Genomics
  • David Kopecký, Institute of Experimental Botany
  • Jan Bartoš, Institute of Experimental Botany
  • Adam J. Lukaszewski, University of California, Riverside
  • James H. Baird, University of California, Riverside
  • Vladimír Černoch, Šlechtitelská stanice Hladké Životice
  • Roland Kölliker, Agroscope Reckenholz Tanikon Research Station ART
  • Odd Arne Rognli, Norwegian University of Life Sciences
  • Helene Blois, Diversity Arrays Technology
  • Vanessa Caig, Diversity Arrays Technology
  • Thomas Lubberstedt, Iowa State University
  • Bruno Studer, University of Aarhus
  • Paul Shaw, Scottish Crop Research Institute
  • Jaroslav Doležel, Institute of Experimental Botany
  • Andrzej Kilian, Diversity Arrays Technology
Document Type
Article
Publication Date
2-5-2009
DOI
10.1186/1471-2164-10-473
Abstract

Background

Grasses are among the most important and widely cultivated plants on Earth. They provide high quality fodder for livestock, are used for turf and amenity purposes, and play a fundamental role in environment protection. Among cultivated grasses, species within the Festuca-Lolium complex predominate, especially in temperate regions. To facilitate high-throughput genome profiling and genetic mapping within the complex, we have developed a Diversity Arrays Technology (DArT) array for five grass species: F. pratensis, F. arundinacea, F. glaucescens, L. perenne and L. multiflorum. Results

The DArTFest array contains 7680 probes derived from methyl-filtered genomic representations. In a first marker discovery experiment performed on 40 genotypes from each species (with the exception of F. glaucescens for which only 7 genotypes were used), we identified 3884 polymorphic markers. The number of DArT markers identified in every single genotype varied from 821 to 1852. To test the usefulness of DArTFest array for physical mapping, DArT markers were assigned to each of the seven chromosomes of F. pratensis using single chromosome substitution lines while recombinants of F. pratensis chromosome 3 were used to allocate the markers to seven chromosome bins. Conclusion

The resources developed in this project will facilitate the development of genetic maps in Festuca and Lolium, the analysis on genetic diversity, and the monitoring of the genomic constitution of the Festuca × Lolium hybrids. They will also enable marker-assisted selection for multiple traits or for specific genome regions.

Comments

This article is published as Kopecký, David, Jan Bartoš, Adam J. Lukaszewski, James H. Baird, Vladimír Černoch, Roland Kölliker, Odd Arne Rognli et al. "Development and mapping of DArT markers within the Festuca-Lolium complex." BMC genomics 10, no. 1 (2009): 473. doi:10.1186/1471-2164-10-473, Posted with permission.

Creative Commons License
Creative Commons Attribution 4.0 International
Copyright Owner
Kopecký et al
Language
en
File Format
application/pdf
Citation Information
David Kopecký, Jan Bartoš, Adam J. Lukaszewski, James H. Baird, et al.. "Development and mapping of DArT markers within the Festuca - Lolium complex" BMC Genomics Vol. 10 Iss. 473 (2009)
Available at: http://works.bepress.com/thomas-lubberstedt/26/