Discovery of Resistance Genes in Rye by Targeted Long-Read Sequencing and Association Genetics

被引:12
|
作者
Vendelbo, Nikolaj M. [1 ,2 ]
Mahmood, Khalid [1 ]
Steuernagel, Burkhard [3 ]
Wulff, Brande B. H. [3 ,4 ,5 ]
Sarup, Pernille [1 ]
Hovmoller, Mogens S. [2 ]
Justesen, Annemarie Fejer [2 ]
Kristensen, Peter S. [1 ]
Orabi, Jihad [1 ]
Jahoor, Ahmed [1 ,6 ]
机构
[1] Nordic Seed AS, Dept Mol Breeding, DK-8300 Odder, Denmark
[2] Aarhus Univ, Fac Technol, Dept Agroecol, DK-4200 Slagelse, Denmark
[3] John Innes Ctr, Norwich Res Pk, Norwich NR4 7UH, Norfolk, England
[4] King Abdullah Univ Sci & Technol KAUST, Biol & Environm Sci & Engn Div, Plant Sci Program, Thuwal 239556900, Saudi Arabia
[5] King Abdullah Univ Sci & Technol KAUST, Ctr Desert Agr, Thuwal 239556900, Saudi Arabia
[6] Swedish Univ Agr Sci, Dept Plant Breeding, SE-23422 Alnarp, Sweden
基金
英国生物技术与生命科学研究理事会;
关键词
Secale cereale L; leaf rust; brown rust; Puccinia recondita f. sp. secalis; nucleotide-binding leucine-rich repeat (NLR); resistance gene enrichment sequencing (RenSeq); single-molecule high-fidelity sequencing (HiFi); genome-wide association study (GWAS); k-mer; LEAF-RUST RESISTANCE; LEUCINE-RICH REPEAT; SECALE-CEREALE L; DISEASE-RESISTANCE; BLIGHT-RESISTANCE; INBRED LINES; COILED-COIL; WHEAT; CLONING; PROTEIN;
D O I
10.3390/cells11081273
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The majority of released rye cultivars are susceptible to leaf rust because of a low level of resistance in the predominant hybrid rye-breeding gene pools Petkus and Carsten. To discover new sources of leaf rust resistance, we phenotyped a diverse panel of inbred lines from the less prevalent Gulzow germplasm using six distinct isolates of Puccinia recondita f. sp. secalis and found that 55 out of 92 lines were resistant to all isolates. By performing a genome-wide association study using 261,406 informative SNP markers, we identified five resistance-associated QTLs on chromosome arms 1RS, 1RL, 2RL, 5RL and 7RS. To identify candidate Puccinia recondita (Pr) resistance genes in these QTLs, we sequenced the rye nucleotide-binding leucine-rich repeat (NLR) intracellular immune receptor complement using a Triticeae NLR bait-library and PacBio (R) long-read single-molecule high-fidelity (HiFi) sequencing. Trait-genotype correlations across 10 resistant and 10 susceptible lines identified four candidate NLR-encoding Pr genes. One of these physically co-localized with molecular markers delimiting Pr3 on chromosome arm 1RS and the top-most resistance-associated QTL in the panel.
引用
收藏
页数:21
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