ArticleTAG. Theoretical and applied genetics. Theoretische und angewandte Genetik2022
Identification and fine mapping of a major QTL (qRtsc8-1) conferring resistance to maize tar spot complex and validation of production markers in breeding lines.
Article in TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Endophytic Beauveria bassiana in maize: influence of genotype, fungal source, inoculation methods, and time on colonization and fitness of Fall armyworm.Scientific reports · 2026Article
- Mining genomic regions associated with stomatal traits and their candidate genes in bread wheat through genome-wide association study (GWAS).TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2025Article
- Tar spot susceptibility of corn influences phyllosphere-associated bacterial and fungal microbiomes.Frontiers in microbiology · 2025Article
- Mining for QTL controlling maize low-phosphorus response genes combined with deep resequencing of RIL parental genomes and in silico GWAS analysis.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2024Article
- KASP: a high-throughput genotyping system and its applications in major crop plants for biotic and abiotic stress tolerance.Molecular biology reports · 2024Review
- Linkage mapping and genomic prediction of grain quality traits in tropical maize (Frontiers in genetics · 2024Article
- Low-Density Reference Fingerprinting SNP Dataset of CIMMYT Maize Lines for Quality Control and Genetic Diversity Analyses.Plants (Basel, Switzerland) · 2022Article
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14 authors.
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Abstract
key messageA major QTL of qRtsc8-1 conferring TSC resistance was identified and fine mapped to a 721 kb region on chromosome 8 at 81 Mb, and production markers were validated in breeding lines. Tar spot complex (TSC) is a major foliar disease of maize in many Central and Latin American countries and leads to severe yield loss. To dissect the genetic architecture of TSC resistance, a genome-wide association study (GWAS) panel and a bi-parental doubled haploid population were used for GWAS and selective genotyping analysis, respectively. A total of 115 SNPs in bin 8.03 were detected by GWAS and three QTL in bins 6.05, 6.07, and 8.03 were detected by selective genotyping. The major QTL qRtsc8-1 located in bin 8.03 was detected by both analyses, and it explained 14.97% of the phenotypic variance. To fine map qRtsc8-1, the recombinant-derived progeny test was implemented. Recombinations in each generation were backcrossed, and the backcross progenies were genotyped with Kompetitive Allele Specific PCR (KASP) markers and phenotyped for TSC resistance individually. The significant tests for comparing the TSC resistance between the two classes of progenies with and without resistant alleles were used for fine mapping. In BC
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