Fine-Mapping the Wheat Snn1 Locus Conferring Sensitivity to the Parastagonospora nodorum Necrotrophic Effector SnTox1 Using an Eight Founder Multiparent Advanced Generation Inter-Cross Population

被引:29
作者
Cockram, James [1 ]
Scuderi, Alice [1 ,2 ]
Barber, Toby [1 ]
Furuki, Eiko [3 ]
Gardner, Keith A. [1 ]
Gosman, Nick [1 ]
Kowalczyk, Radoslaw [1 ,4 ]
Phan, Huyen P. [3 ]
Rose, Gemma A. [1 ]
Tan, Kar-Chun [3 ]
Oliver, Richard P. [3 ]
Mackay, Ian J. [1 ]
机构
[1] NIAB, John Bingham Lab, Cambridge CB3 0LE, England
[2] Univ Messina, Dept Drug Sci & Prod Hlth, I-98122 Messina, Sicily, Italy
[3] Curtin Univ, Ctr Crop Dis Management, Perth, WA 6845, Australia
[4] Univ Manchester, Fac Life Sci, Manchester M13 9PL, Lancs, England
基金
英国生物技术与生命科学研究理事会;
关键词
fungal protein effectors; diagnostic genetic markers; plant disease resistance breeding; multiparent genetic mapping populations; high-density crop genotyping; MPP; Multiparent Advanced Generation Inter-Cross (MAGIC); multiparental populations; PYRENOPHORA-TRITICI-REPENTIS; HOST-SELECTIVE TOXIN; STAGONOSPORA-NODORUM; TAN SPOT; TRIGGERED SUSCEPTIBILITY; GENETIC-ANALYSIS; CAUSAL AGENT; POLYMORPHISM; PURIFICATION; PREVALENCE;
D O I
10.1534/g3.115.021584
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The necrotrophic fungus Parastagonospora nodorum is an important pathogen of one of the world's most economically important cereal crops, wheat (Triticum aestivum L.). P. nodorum produces necrotrophic protein effectors that mediate host cell death, providing nutrients for continuation of the infection process. The recent discovery of pathogen effectors has revolutionized disease resistance breeding for necrotrophic diseases in crop species, allowing often complex genetic resistance mechanisms to be broken down into constituent parts. To date, three effectors have been identified in P. nodorum. Here we use the effector, SnTox1, to screen 642 progeny from an eight-parent multiparent advanced generation inter-cross (i.e., MAGIC) population, genotyped with a 90,000-feature single-nucleotide polymorphism array. The MAGIC founders showed a range of sensitivity to SnTox1, with transgressive segregation evident in the progeny. SnTox1 sensitivity showed high heritability, with quantitative trait locus analyses fine-mapping the Snn1 locus to the short arm of chromosome 1B. In addition, a previously undescribed SnTox1 sensitivity locus was identified on the long arm of chromosome 5A, termed here QSnn.niab-5A.1. The peak single-nucleotide polymorphism for the Snn1 locus was converted to the KASP genotyping platform, providing breeders and researchers a simple and cheap diagnostic marker for allelic state at Snn1.
引用
收藏
页码:2257 / 2266
页数:10
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