Abstract

BackgroundCrown rust, caused by Puccinia coronata f. sp. avenae, is the most important disease of oat worldwide. Adult plant resistance (APR), based upon partial resistance, has proven to be a durable rust management strategy in other cereal rust pathosystems. The crown rust APR in the oat line MN841801 has been effective for more than 30 years. The genetic basis of this APR was studied under field conditions in three recombinant inbred line (RIL) populations: 1) AC Assiniboia/MN841801, 2) AC Medallion/MN841801, and 3) Makuru/MN841801. The populations were evaluated for crown rust resistance with the crown rust isolate CR251 (race BRBB) in multiple environments. The 6 K oat and 90 K wheat Illumina Infinium single nucleotide polymorphism (SNP) arrays were used for genotyping the AC Assiniboia/MN841801 population. KASP assays were designed for selected SNPs and genotyped on the other two populations.ResultsThis study reports a high density genetic linkage map constructed with oat and wheat SNP markers in the AC Assiniboia/MN841801 RIL population. Most wheat SNPs were monomorphic in the oat population. However the polymorphic wheat SNPs could be scored accurately and integrated well into the linkage map. A major quantitative trait locus (QTL) on oat chromosome 14D, designated QPc.crc-14D, explained up to 76% of the APR phenotypic variance. This QTL is flanked by two SNP markers, GMI_GBS_90753 and GMI_ES14_c1439_83. QPc.crc-14D was validated in the populations AC Medallion/MN841801 and Makuru/MN841801.ConclusionsWe report the first APR QTL in oat with a large and consistent effect. QPc.crc-14D was statistically significant in all environments tested in each of the three oat populations. QPc.crc-14D is a suitable candidate for use in marker-assisted breeding and also an excellent target for map-based cloning. This is also the first study to use the 90 K wheat Infinium SNP array on oat for marker development and comparative mapping. The Infinium SNP array is a useful tool for saturating oat maps with markers. Synteny with wheat suggests that QPc.crc-14D is orthologous with the stripe rust APR gene Yr16 in wheat.Electronic supplementary materialThe online version of this article (doi:10.1186/s12870-014-0250-2) contains supplementary material, which is available to authorized users.

Highlights

  • Crown rust, caused by Puccinia coronata f. sp. avenae, is the most important disease of oat worldwide

  • Crown rust caused by Puccinia coronata Corda f. sp. avenae Eriks. is the most economically important disease of cultivated oat (Avena sativa L.) [1,2]

  • The objectives of this research were to: 1) develop a whole-genome genetic linkage map for an AC Assiniboia/ MN841801 population using the 6 K oat and 90 K wheat Infinium single nucleotide polymorphism (SNP) genotyping assays, 2) detect and characterize quantitative trait locus (QTL) for crown rust adult plant resistance (APR) from MN841801 in the AC Assiniboia/MN841801 population, 3) validate the QTL using Kompetitive Allele Specific PCR (KASP) SNP genotyping in two additional Recombinant inbred line (RIL) populations (AC Medallion/MN841801 and Makuru/MN841801), and 4) predict orthologous wheat APR genes

Read more

Summary

Introduction

Crown rust, caused by Puccinia coronata f. sp. avenae, is the most important disease of oat worldwide. Avenae, is the most important disease of oat worldwide. Adult plant resistance (APR), based upon partial resistance, has proven to be a durable rust management strategy in other cereal rust pathosystems. The crown rust APR in the oat line MN841801 has been effective for more than 30 years. Is the most economically important disease of cultivated oat (Avena sativa L.) [1,2]. Resistant oat varieties are an important control strategy for managing this disease. Partial resistance is more difficult to use in plant breeding because the breeder must select for quantitative differences in disease reaction. Adult plant partial resistance can be confused with complete resistance that is only effective against a portion of the pathogen population present in a field nursery

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call