Next-generation sequencing identified genomic region and diagnostic markers for resistance to bacterial wilt on chromosome B02 in peanut (Arachis hypogaea L.)

被引:52
|
作者
Luo, Huaiyong [1 ]
Pandey, Manish K. [2 ]
Khan, Aamir W. [2 ]
Wu, Bei [1 ]
Guo, Jianbin [1 ]
Ren, Xiaoping [1 ]
Zhou, Xiaojing [1 ]
Chen, Yuning [1 ]
Chen, Weigang [1 ]
Huang, Li [1 ]
Liu, Nian [1 ]
Lei, Yong [1 ]
Liao, Boshou [1 ]
Varshney, Rajeev K. [2 ]
Jiang, Huifang [1 ]
机构
[1] Chinese Acad Agr Sci, Key Lab Biol & Genet Improvement Oil Crops, Minist Agr, Oil Crops Res Inst, Wuhan, Hubei, Peoples R China
[2] Int Crops Res Inst Semi Arid Trop, Hyderabad, India
基金
中国国家自然科学基金;
关键词
peanut; bacterial wilt resistance; QTL-seq; candidate genes; diagnostic markers; QUANTITATIVE DISEASE RESISTANCE; CONTROLLING SHELLING PERCENTAGE; RALSTONIA-SOLANACEARUM; ARABIDOPSIS-THALIANA; RAPID IDENTIFICATION; CANDIDATE GENES; TRAIT LOCI; PROTEIN; QTL; KINASE;
D O I
10.1111/pbi.13153
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Bacterial wilt, caused by Ralstonia solanacearum, is a devastating disease affecting over 350 plant species. A few peanut cultivars were found to possess stable and durable bacterial wilt resistance (BWR). Genomics-assisted breeding can accelerate the process of developing resistant cultivars by using diagnostic markers. Here, we deployed sequencing-based trait mapping approach, QTL-seq, to discover genomic regions, candidate genes and diagnostic markers for BWR in a recombination inbred line population (195 progenies) of peanut. The QTL-seq analysis identified one candidate genomic region on chromosome B02 significantly associated with BWR. Mapping of newly developed single nucleotide polymorphism (SNP) markers narrowed down the region to 2.07 Mb and confirmed its major effects and stable expressions across three environments. This candidate genomic region had 49 nonsynonymous SNPs affecting 19 putative candidate genes including seven putative resistance genes (R-genes). Two diagnostic markers were successfully validated in diverse breeding lines and cultivars and could be deployed in genomics-assisted breeding of varieties with enhanced BWR.
引用
收藏
页码:2356 / 2369
页数:14
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