Molecular mapping of QTLs for resistance to the greenbug Schizaphis graminum (Rondani) in Sorghum bicolor (Moench)

• Published in: Theoretical and applied genetics 2008-06, Vol.117 (1), p.117-124
• Main Authors: Wu, Yanqi, Huang, Yinghua
• Format: Article
• Language: English
• Subjects: Agriculture; Animals; Aphids; Biochemistry; Biological and medical sciences; Biomedical and Life Sciences; Biotechnology; Chromosome Mapping; Chromosomes, Plant - genetics; Classical genetics, quantitative genetics, hybrids; Cloning; Crosses, Genetic; DNA, Plant - genetics; Fundamental and applied biological sciences. Psychology; Genes; Genetic Linkage; Genetic Markers; Genetic Variation; Genetics of eukaryotes. Biological and molecular evolution; Genotype; Grain; Life Sciences; Methods, theories and miscellaneous; Minisatellite Repeats; Original Paper; Phenotype; Plant Biochemistry; Plant Breeding/Biotechnology; Plant Genetics and Genomics; Pteridophyta, spermatophyta; Quantitative Trait Loci; Seeds; Soil sciences; Sorghum; Sorghum - genetics; Vegetals
• ISSN: 0040-5752; 1432-2242
• DOI: 10.1007/s00122-008-0757-8

Sorghum is a worldwide important cereal crop and widely cultivated for grain and forage production. Greenbug, Schizaphis graminum (Rondani) is one of the major insect pests of sorghum and can cause serious damage to sorghum plants, particularly in the US Great Plains. Identification of chromosomal regions responsible for greenbug resistance will facilitate both map-based cloning and marker-assisted breeding. Thus, a mapping experiment was conducted to dissect sorghum genetic resistance to greenbug biotype I into genomic regions. Two hundred and seventy-seven (277) F₂ progeny and their F₂:₃ families from a cross between Westland A line (susceptible parent) and PI550610 (resistant parent) combined with 118 polymorphic simple sequence repeat (SSR) markers were used to map the greenbug resistance QTLs. Composite interval mapping (CIM) and multiple interval mapping (MIM) revealed two QTLs on sorghum chromosome nine (SBI-09) consistently conditioned the resistance of host plant to the greenbug. The two QTLs were designated as QSsgr-09-01 (major QTL) and QSsgr-09-02 (minor QTL), accounting for approximately 55-80%, and 1-6% of the phenotypic variation for the resistance to greenbug feeding, respectively. These resistance QTLs appeared to have additive and partially dominant effects. The markers Xtxp358, Xtxp289, Xtxp67 and Xtxp230 closely flanked the respective QTLs, and can be used in high-throughput marker-assisted selections (MAS) for breeding new resistant parents and producing commercial hybrids.