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Construction of a dense genetic map of the Malus fusca fire blight resistant accession MAL0045 using tunable genotyping-by-sequencing SNPs and microsatellites

GND
1211645738
Zugehörigkeit
Julius Kühn-Institute (JKI), Institute for Breeding Research on Fruit Crops, Germany
Emeriewen, Ofere Francis;
GND
1059141744
Zugehörigkeit
Julius Kühn-Institute (JKI), Institute for Resistance Research and Stress Tolerance, Germany
Richter, Klaus;
GND
1172920559
Zugehörigkeit
Julius Kühn-Institute (JKI), Institute for Biosafety in Plant Biotechnology, Germany
Berner, Thomas;
GND
1013858662
Zugehörigkeit
Julius Kühn-Institute (JKI), Institute for Biosafety in Plant Biotechnology, Germany
Keilwagen, Jens;
Zugehörigkeit
Data2Bio LLC, USA ; Plant Sciences Institute, Iowa State University, USA
Schnable, Patrick S.;
Zugehörigkeit
Research and Innovation Centre, Genomics and Biology of Fruit Crops Department, Fondazione Edmund Mach, Italy
Malnoy, Mickael;
GND
172861896
Zugehörigkeit
Julius Kühn-Institute (JKI), Institute for Breeding Research on Fruit Crops, Germany
Peil, Andreas

Although, the Pacific crabapple, Malus fusca, is a hardy and disease resistant species, studies relating to the genetics of its unique traits are very limited partly due to the lack of a genetic map of this interesting wild apple. An accession of M. fusca (MAL0045) of Julius Kühn-Institut collection in Germany is highly resistant to fire blight disease, incited by different strains of the causative pathogen—Erwinia amylovora. This is the most destructive bacterial disease of Malus of which most of the domesticated apples (Malus domestica) are susceptible. Using a scarcely dense genetic map derived from a population of 134 individuals of MAL0045 × ‘Idared’, the locus (Mfu10) controlling fire blight resistance mapped on linkage group 10 (LG10) and explained up to 66% of the phenotypic variance with different strains. Although the development of robust and tightly linked molecular markers on LG10 through chromosome walking approach led to the identification of a major candidate gene, any minor effect locus remained elusive possibly due to the lack of marker density of the entire genetic map. Therefore, we have developed a dense genetic map of M. fusca using tunable genotyping-by-sequencing (tGBS) approach. Of thousands of de novo SNPs identified, 2677 were informative in M. fusca and 90.5% of these successfully mapped. In addition, integration of SNP data and microsatellite (SSR) data resulted in a final map comprising 17 LGs with 613 loci spanning 1081.35 centi Morgan (cM). This map will serve as a template for mapping using different strains of the pathogen.

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