BED-domain-containing immune receptors confer diverse resistance spectra to yellow rust

被引:242
作者
Marchal, Clemence [1 ]
Zhang, Jianping [2 ,3 ,4 ]
Zhang, Peng [2 ]
Fenwick, Paul [5 ]
Steuernagel, Burkhard [1 ]
Adamski, Nikolai M. [1 ]
Boyd, Lesley [6 ]
McIntosh, Robert [2 ]
Wulff, Brande B. H. [1 ]
Berry, Simon [5 ]
Lagudah, Evans [3 ]
Uauy, Cristobal [1 ]
机构
[1] John Innes Ctr, Norwich Res Pk, Norwich, Norfolk, England
[2] Univ Sydney, Plant Breeding Inst, Cobbitty, NSW, Australia
[3] Commonwealth Sci & Ind Res Org CSIRO Agr & Food, Canberra, ACT, Australia
[4] Henan Tianmin Seed Co Ltd, Lankao Cty, Henan, Peoples R China
[5] Limagrain UK Ltd, Market Rasen, Lincs, England
[6] NIAB, Cambridge, England
基金
英国生物技术与生命科学研究理事会; 美国国家科学基金会;
关键词
F-SP TRITICI; PATHOGEN EFFECTORS; HEXAPLOID WHEAT; BREAD WHEAT; GENE; SEQUENCE; LOCUS; IDENTIFICATION; INTEGRATION; EXPRESSION;
D O I
10.1038/s41477-018-0236-4
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Crop diseases reduce wheat yields by similar to 25% globally and thus pose a major threat to global food security(1). Genetic resistance can reduce crop losses in the field and can be selected through the use of molecular markers. However, genetic resistance often breaks down following changes in pathogen virulence, as experienced with the wheat yellow (stripe) rust fungus Puccinia striiformis f. sp. tritici (Pst)(2). This highlights the need to (1) identify genes that, alone or in combination, provide broad-spectrum resistance, and (2) increase our understanding of the underlying molecular modes of action. Here we report the isolation and characterization of three major yellow rust resistance genes (Yr7, Yr5 and YrSP) from hexaploid wheat (Triticum aestivum), each having a distinct recognition specificity. We show that Yr5, which remains effective to a broad range of Pst isolates worldwide, is closely related yet distinct from Yr(7), whereas YrSP is a truncated version of Yr5 with 99.8% sequence identity. All three Yr genes belong to a complex resistance gene cluster on chromosome 2B encoding nucleotide-binding and leucine-rich repeat proteins (NLRs) with a non-canonical N-terminal zinc-finger BED domain(3) that is distinct from those found in non-NLR wheat proteins. We developed diagnostic markers to accelerate haplotype analysis and for marker-assisted selection to expedite the stacking of the non-allelic Yr genes. Our results provide evidence that the BED-NLR gene architecture can provide effective fieldbased resistance to important fungal diseases such as wheat yellow rust.
引用
收藏
页码:662 / 668
页数:7
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