High-density genome-wide association mapping implicates an F-box encoding gene in Medicago truncatula resistance to Aphanomyces euteiches

被引:66
作者
Bonhomme, Maxime [1 ,2 ]
Andre, Olivier [1 ,2 ]
Badis, Yacine [1 ,2 ]
Ronfort, Joelle [3 ]
Burgarella, Concetta [3 ]
Chantret, Nathalie [3 ]
Prosperi, Jean-Marie [3 ]
Briskine, Roman [4 ]
Mudge, Joann [5 ]
Debelle, Frederic [6 ]
Navier, Helene [7 ]
Miteul, Henri [7 ]
Hajri, Ahmed [7 ]
Baranger, Alain [7 ]
Tiffin, Peter [8 ]
Dumas, Bernard [1 ,2 ]
Pilet-Nayel, Marie-Laure [7 ]
Young, Nevin D. [8 ,9 ]
Jacquet, Christophe [1 ,2 ]
机构
[1] Univ Toulouse, Lab Rech Sci Vegetales, UPS, F-31326 Castanet Tolosan, France
[2] CNRS, Lab Rech Sci Vegetales, F-31326 Castanet Tolosan, France
[3] INRA, UMR AGAP, F-34060 Montpellier, France
[4] Univ Minnesota, Dept Comp Sci & Engn, St Paul, MN 55455 USA
[5] Natl Ctr Genome Resources, Santa Fe, NM 87505 USA
[6] INRA, LIPM, UMR441, F-31326 Castanet Tolosan, France
[7] INRA, UMR IGEPP 1349, F-35653 Le Rheu, France
[8] Univ Minnesota, Dept Plant Biol, St Paul, MN 55108 USA
[9] Univ Minnesota, Dept Plant Pathol, St Paul, MN 55108 USA
基金
美国国家科学基金会;
关键词
Aphanomyces euteiches; F-box protein; Genome-wide association study; Medicago truncatula; oomycete; partial resistance; root; QUANTITATIVE DISEASE RESISTANCE; TRANSCRIPTION FACTOR MYB30; MODEL LEGUME; POPULATION-STRUCTURE; NATURAL VARIATION; DEFENSE RESPONSE; COMPLEX TRAITS; PISUM-SATIVUM; PLANT-DISEASE; SELECTION;
D O I
10.1111/nph.12611
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The use of quantitative disease resistance (QDR) is a promising strategy for promoting durable resistance to plant pathogens, but genes involved in QDR are largely unknown. To identify genetic components and accelerate improvement of QDR in legumes to the root pathogen Aphanomyces euteiches, we took advantage of both the recently generated massive genomic data for Medicago truncatula and natural variation of this model legume. A high-density (approximate to 5.1 million single nucleotide polymorphisms (SNPs)) genome-wide association study (GWAS) was performed with both in vitro and glasshouse phenotyping data collected for 179 lines. GWAS identified several candidate genes and pinpointed two independent major loci on the top of chromosome 3 that were detected in both phenotyping methods. Candidate SNPs in the most significant locus (sigma(2)(A) = 23%) were in the promoter and coding regions of an F-box protein coding gene. Subsequent qRT-PCR and bioinformatic analyses performed on 20 lines demonstrated that resistance is associated with mutations directly affecting the interaction domain of the F-box protein rather than gene expression. These results refine the position of previously identified QTL to specific candidate genes, suggest potential molecular mechanisms, and identify new loci explaining QDR against A. euteiches.
引用
收藏
页码:1328 / 1342
页数:15
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