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高密度全基因组关联图谱定位表明,蒺藜苜蓿中一个编码F-box的基因与对豌豆根腐病菌的抗性有关。

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

作者信息

Bonhomme Maxime, André Olivier, Badis Yacine, Ronfort Joëlle, Burgarella Concetta, Chantret Nathalie, Prosperi Jean-Marie, Briskine Roman, Mudge Joann, Debéllé Frédéric, Navier Hélène, Miteul Henri, Hajri Ahmed, Baranger Alain, Tiffin Peter, Dumas Bernard, Pilet-Nayel Marie-Laure, Young Nevin D, Jacquet Christophe

机构信息

UPS, Laboratoire de Recherche en Sciences Végétales, Université de Toulouse, BP42617, Auzeville, F-31326, Castanet-Tolosan, France.

CNRS, Laboratoire de Recherche en Sciences Végétales, BP42617, Auzeville, F-31326, Castanet-Tolosan, France.

出版信息

New Phytol. 2014 Mar;201(4):1328-1342. doi: 10.1111/nph.12611. Epub 2013 Nov 28.

DOI:10.1111/nph.12611
PMID:24283472
Abstract

• 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 (≈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 (σ(A)²= 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.

摘要

• 利用数量抗病性(QDR)是促进对植物病原体产生持久抗性的一种有前景的策略,但参与QDR的基因大多未知。为了鉴定豆科植物对根病原体腐皮镰孢菌(Aphanomyces euteiches)的QDR的遗传成分并加速其改良,我们利用了最近生成的截形苜蓿(Medicago truncatula)大量基因组数据以及这种模式豆科植物的自然变异。

• 对179个株系收集的体外和温室表型数据进行了高密度(约510万个单核苷酸多态性(SNP))全基因组关联研究(GWAS)。

• GWAS鉴定出几个候选基因,并在3号染色体顶端确定了两个独立的主要位点,这两个位点在两种表型分析方法中均被检测到。最显著位点(σ(A)² = 23%)中的候选SNP位于一个F-box蛋白编码基因的启动子和编码区。随后对20个株系进行的qRT-PCR和生物信息学分析表明,抗性与直接影响F-box蛋白相互作用结构域的突变相关,而非与基因表达相关。

• 这些结果将先前鉴定的QTL的位置细化到特定候选基因,提示了潜在的分子机制,并鉴定出了解释对腐皮镰孢菌QDR的新位点。

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