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

被引:16
作者
Emeriewen, Ofere Francis [1 ]
Richter, Klaus [2 ]
Berner, Thomas [3 ]
Keilwagen, Jens [3 ]
Schnable, Patrick S. [4 ,5 ]
Malnoy, Mickael [6 ]
Peil, Andreas [1 ]
机构
[1] Julius Kuhn Inst JKI, Inst Breeding Res Fruit Crops, Fed Res Ctr Cultivated Plant, Pillnitzer Pl 3a, D-01326 Dresden, Germany
[2] Julius Kuhn Inst JKI, Inst Resistance Res & Stress Tolerance, Fed Res Ctr Cultivated Plants, Erwin Baur Str 27, D-06484 Quedlinburg, Germany
[3] Julius Kuhn Inst JKI, Inst Biosafety Plant Biotechnol, Fed Res Ctr Cultivated Plants, Erwin Baur Str 27, D-06484 Quedlinburg, Germany
[4] Data2Bio LLC, Ames, IA 50011 USA
[5] Iowa State Univ, Plant Sci Inst, 2035B Carver, Ames, IA 50011 USA
[6] Fdn Edmund Mach, Genom & Biol Fruit Crops Dept, Res & Innovat Ctr, Via E Mach 1, I-38010 San Michele All Adige, Trentino, Italy
关键词
X ROBUSTA 5; LINKAGE MAPS; APPLE; QTL; GENOME; INOCULATION; ROSACEAE;
D O I
10.1038/s41598-020-73393-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 Kuhn-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 MAL0045x'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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页数:10
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