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Identification of a QTL region for ashy stem blight resistance using genome-wide association and linage analysis in common bean recombinant inbred lines derived from BAT 477 and NY6020-4
被引:4
|作者:
Viteri, Diego M. M.
[1
]
Linares, Angela M. M.
[2
]
Miranda, Zoralys
[1
]
Shi, Ainong
[3
]
机构:
[1] Univ Puerto Rico, Dept Agroenvironm Sci, Isabela Res Substn, Isabela, PR 00662 USA
[2] Univ Puerto Rico, Dept Agroenvironm Sci, Lajas Res Substn, Lajas, PR USA
[3] Univ Arkansas, Dept Hort, Fayetteville, AR 72701 USA
来源:
关键词:
ashy stem blight;
common bean;
Macrophomina phaseolina;
Phaseolus vulgaris;
quantitative trait loci;
genome-wide association study;
PHASEOLINA TASSI GOID;
MACROPHOMINA-PHASEOLINA;
FIELD-RESISTANCE;
WHITE MOLD;
INHERITANCE;
PATHOGENESIS;
VARIABILITY;
D O I:
10.3389/fpls.2022.1019263
中图分类号:
Q94 [植物学];
学科分类号:
071001 ;
摘要:
Ashy stem blight (ASB), caused by the fungus Macrophomina phaseolina (Tassi) Goidanich is an important disease of the common bean (Phaseolus vulgaris L.). It is important to identify quantitative trait loci (QTL) for ASB resistance and introgress into susceptible cultivars of the common bean. The objective of this research was to identify QTL and single nucleotide polymorphism (SNP) markers associated with ASB resistance in recombinant inbred lines (RIL) derived from a cross between BAT 477 and NY6020-4 common bean. One hundred and twenty-six F-6 : 7 RIL were phenotyped for ASB in the greenhouse. Disease severity was scored on a scale of 1-9. Genotyping was performed using whole genome resequencing with 2x common bean genome size coverage, and over six million SNPs were obtained. After being filtered, 72,017 SNPs distributed on 11 chromosomes were used to conduct the genome-wide association study (GWAS) and QTL mapping. A novel QTL region of similar to 4.28 Mbp from 35,546,329 bp to 39,826,434 bp on chromosome Pv03 was identified for ASB resistance. The two SNPs, Chr03_39824257 and Chr03_39824268 located at 39,824,257 bp and 39,824,268 bp on Pv03, respectively, were identified as the strongest markers associated with ASB resistance. The gene Phvul.003G175900 (drought sensitive, WD repeatcontaining protein 76) located at 39,822,021 - 39,824,655 bp on Pv03 was recognized as one candidate for ASB resistance in the RIL, and the gene contained the two SNP markers. QTL and SNP markers may be used to select plants and lines for ASB resistance through marker-assisted selection (MAS) in common bean breeding.
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页数:15
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