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High‐density genome‐wide association mapping implicates an F ‐box encoding gene in M edicago truncatula resistance to A phanomyces euteiches
Author(s) -
Bonhomme Maxime,
André Olivier,
Badis Yacine,
Ronfort Joëlle,
Burgarella Concetta,
Chantret Nathalie,
Prosperi JeanMarie,
Briskine Roman,
Mudge Joann,
Debéllé Frédéric,
Navier Hélène,
Miteul Henri,
Hajri Ahmed,
Baranger Alain,
Tiffin Peter,
Dumas Bernard,
PiletNayel MarieLaure,
Young Nevin D.,
Jacquet Christophe
Publication year - 2014
Publication title -
new phytologist
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.742
H-Index - 244
eISSN - 1469-8137
pISSN - 0028-646X
DOI - 10.1111/nph.12611
Subject(s) - biology , genetics , genome wide association study , locus (genetics) , quantitative trait locus , gene , single nucleotide polymorphism , candidate gene , genome , computational biology , genotype
Summary 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 A phanomyces euteiches , we took advantage of both the recently generated massive genomic data for M edicago truncatula and natural variation of this model legume. A high‐density (≈5.1 million single nucleotide polymorphisms ( SNP s)) 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 SNP s in the most significant locus ( σ A 2 = 23%) were in the promoter and coding regions of an F ‐box protein coding gene. Subsequent q RT ‐ 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 .