Genome · 1998 · 84 citations · 17 references
AgricultureGeneticsPlant SciencesBreeding For Disease ResistanceGermplasm EvaluationPlant GeneticsMolecular Markers In PlantsPlant Disease ResistanceResistant Crop VarietiesBulk Segregant AnalysisBulked Segregant AnalysisMolecular Markers For ResistancePlant Disease Resistance GenesPlant Resistance GenesRandom Amplified Polymorphic Dna AnalysisRandom Amplified Polymorphic Dna MarkersResistance Trait Evaluation
Powdery mildew is a serious disease of pea caused by the obligate parasite Erysiphe pisi Syd. Random amplified polymorphic DNA (RAPD) analysis has emerged as a cost-effective and efficient marker system. The objective of this study was to identify RAPD markers for powdery mildew resistance gene er-1. The resistant cultivar Highlight (carrying er-1) and the susceptible cultivar Radley were crossed, and F 3 plants were screened with Operon (OP) and University of British Columbia (UBC) primers, using bulked segregant analysis. A total of 416 primers were screened, of which amplicons of three Operon primers, OPO-18, OPE-16, and OPL-6, were found to be linked to er-1. OPO-18 1200 was linked in coupling (trans to er-1) and no recombinants were found. OPE-16 1600 (4 ± 2 cM) and OPL-6 1900 (2 ± 2 cM) were linked in repulsion (cis to er-1). The fragments OPO-18 1200 and OPE-16 1600 were sequenced and specific primers designed. The specific primer pair Sc-OPO-18 1200 will be useful in identifying homozygous resistant individuals in F 2 and subsequent segregating generations. Sc-OPE-16 1600 will have greatest utility in selecting heterozygous BC\dn6 nF 1 individuals in backcross breeding programs.Key words: bulked segregant analysis,Erysiphe pisi, pea, RAPD.
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