Localization of the stem rust resistance gene Pg2 to linkage group Mrg20 in cultivated oat (Avena sativa)
Citation
Kebede, A.Z., Bekele, W.A., Mitchell Fetch, J.W., Beattie, A.D., Chao, S., Tinker, N.A., Fetch, T.G., McCartney, C.A. (2020). Localization of the stem rust resistance gene Pg2 to linkage group Mrg20 in cultivated oat (Avena sativa). Phytopathology, [online] 110(10), 1721-1726. http://dx.doi.org/10.1094/PHYTO-03-20-0076-R
Plain language summary
Stem rust is an important disease of cultivated oat. In North America, genetic resistance is the primary strategy to control this disease. Resistance is conferred by a relatively small number of known resistance genes. Pg2 is a widely deployed stem rust resistance gene that originates from cultivated oat. Oat breeders wish to develop cultivars with multiple resistance genes to slow the breakdown of resistance. To do so requires DNA markers suited for marker-assisted selection. Our objectives were to construct maps for Pg2, develop predictive marker assays, and test the prediction accuracy of those assays with a diverse panel of oat cultivars. Linkage analysis identified a common chromosome location for Pg2 in three oat populations. The most predictive markers were identified and converted to breeder-friendly assays for use in oat breeding programs. When used in combination, these assays were highly predictive of Pg2 in a panel of 54 oat breeding lines and cultivars.
Abstract
Stem rust is an important disease of cultivated oat (Avena sativa) caused by Puccinia graminis f. sp. avenae. In North America, host resistance is the primary strategy to control this disease and is conferred by a relatively small number of resistance genes. Pg2 is a widely deployed stem rust resistance gene that originates from cultivated oat. Oat breeders wish to develop cultivars with multiple Pg genes to slow the breakdown of single gene resistance, and often require DNA markers suited for marker-assisted selection. Our objectives were to (i) construct high density linkage maps for a major oat stem rust resistance gene using three biparental mapping populations, (ii) develop Kompetitive allele-specific PCR (KASP) assays for Pg2-linked single-nucleotide polymorphisms (SNPs), and (iii) test the prediction accuracy of those markers with a diverse panel of spring oat lines and cultivars. Genotyping-bysequencing SNP markers linked to Pg2 were identified in an AC Morgan/ CDC Morrison recombinant inbred line (RIL) population. Pg2-linked SNPs were then analyzed in an AC Morgan/RL815 F2 population and an AC Morgan/CDC Dancer RIL population. Linkage analysis identified a common location for Pg2 in all three populations on linkage group Mrg20 of the oat consensus genetic map. The most predictive markers were identified and converted to KASP assays for use in oat breeding programs. When used in combination, the KASP assays for the SNP loci avgbs2_126549.1.46 and avgbs_cluster_ 23819.1.27 were highly predictive of Pg2 status in panel of 54 oat breeding lines and cultivars.