Detection of QTLs associated with mungbean yellow mosaic virus (MYMV) resistance using the interspecific cross of Vigna radiata x Vigna umbellata

被引:28
作者
Mathivathana, Mayalagu Kanimoli [1 ]
Murukarthick, Jayakodi [2 ]
Karthikeyan, Adhimoolam [3 ]
Jang, Woojong [4 ]
Dhasarathan, Manickam [3 ]
Jagadeeshselvam, Nallathambi [5 ]
Sudha, Manickam [5 ]
Vanniarajan, Chocklingam [1 ]
Karthikeyan, Gandhi [6 ]
Yang, Tae-Jin [4 ]
Raveendran, Muthurajan [5 ]
Pandiyan, Muthaiyan [7 ]
Senthil, Natesan [3 ,8 ]
机构
[1] Tamil Nadu Agr Univ, Agr Coll & Res Inst, Dept Plant Breeding & Genet, Madurai, Tamil Nadu, India
[2] Leibniz Inst Plant Genet & Crop Plant Res IPK Gat, Corrensstr 3, D-06466 Seeland, Germany
[3] Tamil Nadu Agr Univ, Dept Biotechnol, Agr Coll & Res Inst, Madurai, Tamil Nadu, India
[4] Seoul Natl Univ, Plant Genom & Breeding Inst, Res Inst Agr & Life Sci, Coll Agr & Life Sci,Dept Plant Sci, Seoul, South Korea
[5] Tamil Nadu Agr Univ, Dept Plant Biotechnol, Ctr Plant Mol Biol & Biotechnol, Coimbatore, Tamil Nadu, India
[6] Tamil Nadu Agr Univ, Dept Plant Pathol, Ctr Plant Protect Studies, Coimbatore, Tamil Nadu, India
[7] Tamil Nadu Agr Univ, Agr Coll & Res Inst, Thanjavur, Tamil Nadu, India
[8] Tamil Nadu Agr Univ, Dept Plant Mol Biol & Bioinformat, Ctr Plant Mol Biol & Biotechnol, Coimbatore, Tamil Nadu, India
关键词
Genotyping by sequencing; Interspecific hybridization; Mungbean; Mungbean yellow mosaic virus; Ricebean; Single nucleotide polymorphism; QUANTITATIVE TRAIT LOCUS; DISEASE RESISTANCE; L; WILCZEK; DEFENSE RESPONSES; GENE; MAP; IDENTIFICATION; INVOLVEMENT; CLONING; PHASE;
D O I
10.1007/s13353-019-00506-x
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
Mungbean (Vigna radiata) and ricebean (V. umbellata) were utilized to obtain an inter-specific recombinant inbred line (RIL) population with the objective of detecting quantitative trait loci (QTL) associated with mungbean yellow mosaic virus (MYMV) resistance. To precisely map QTLs, accurate genetic linkage maps are essential. In the present study, genotyping-by-sequencing (GBS) platform was utilized to develop the genetic linkage map. The map contained 538 single nucleotide polymorphism (SNP) markers, consisted of 11 linkage groups and spanned for 1291.7 cM with an average marker distance of 2.40 cM. The individual linkage group ranged from 90.2 to 149.1 cM in length, and the SNP markers were evenly distributed in the genetic linkage map, with 30-79 SNP markers per chromosome. The QTL analysis using the genetic map and 2 years (2015 and 2016) of phenotyping data identified five QTLs with phenotypic variation explained (PVE) from 10.11 to 20.04%. Of these, a QTL on chromosome 4, designated as qMYMV4-1, was major and stably detected in the same marker interval in both years. This QTL region harbours possible candidate genes for controlling MYMV resistance. The linkage map and QTL/gene (s) for MYMV resistance identified in this study should be useful for QTL fine mapping and cloning for further studies.
引用
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页码:255 / 268
页数:14
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