Confirmation and Fine Mapping of a Major QTL for Aflatoxin Resistance in Maize Using a Combination of Linkage and Association Mapping

被引:19
作者
Zhang, Yu [1 ]
Cui, Min [1 ]
Zhang, Jimin [2 ]
Zhang, Lei [1 ]
Li, Chenliu [1 ]
Kan, Xin [1 ]
Sun, Qian [1 ]
Deng, Dexiang [1 ]
Yin, Zhitong [1 ]
机构
[1] Yangzhou Univ, Jiangsu Key Lab Crop Genet & Physiol, Coinnovat Ctr Modern Prod Technol Grain Crops, Key Lab Plant Funct Genom,Minist Educ, Yangzhou 225009, Jiangsu, Peoples R China
[2] Zhenjiang BGI Fisheries Sci & Technol Ind Co Ltd, Zhenjiang 212000, Peoples R China
基金
中国国家自然科学基金;
关键词
Aspergillus; flavus (A.flavus); genome-wide association analysis (GWAS); linkage mapping; maize; molecular marker; quantitative trait locus (QTL); recombinant inbred line (RIL); QUANTITATIVE TRAIT LOCI; ASPERGILLUS-FLAVUS INFECTION; CONTRIBUTING RESISTANCE; ACCUMULATION; IDENTIFICATION; CONTAMINATION; INHERITANCE; CORN;
D O I
10.3390/toxins8090258
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Maize grain contamination with aflatoxin from Aspergillusflavus (A. flavus) is a serious health hazard to animals and humans. To map the quantitative trait loci (QTLs) associated with resistance to A. flavus, we employed a powerful approach that differs from previous methods in one important way: it combines the advantages of the genome-wide association analysis (GWAS) and traditional linkage mapping analysis. Linkage mapping was performed using 228 recombinant inbred lines (RILs), and a highly significant QTL that affected aflatoxin accumulation, qAA8, was mapped. This QTL spanned approximately 7 centi-Morgan (cM) on chromosome 8. The confidence interval was too large for positional cloning of the causal gene. To refine this QTL, GWAS was performed with 558,629 single nucleotide polymorphisms (SNPs) in an association population comprising 437 maize inbred lines. Twenty-five significantly associated SNPs were identified, most of which co-localised with qAA8 and explained 6.7% to 26.8% of the phenotypic variation observed. Based on the rapid linkage disequilibrium (LD) and the high density of SNPs in the association population, qAA8 was further localised to a smaller genomic region of approximately 1500 bp. A high-resolution map of the qAA8 region will be useful towards a marker-assisted selection (MAS) of A. flavus resistance and a characterisation of the causal gene.
引用
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页数:15
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