Genome · 2007 · 82 citations · 36 references
Life SciencesGeneticsPlant SciencesBreeding For Disease ResistanceCrop ImprovementPlant GeneticsGene MappingGenetic MappingGermplasm CharacterizationMolecular Markers In PlantsPlant Breeding GeneticsAmplified Fragment Length Polymorphism MarkersGenetic Linkage Map ConstructionGenetic Mapping PopulationsRestriction Fragment Length Polymorphism AnalysisRestriction Fragment Length Polymorphism MappingSequence-tagged Site MarkersSimple Sequence Repeat AnalysisSimple Sequence Repeats
A high-resolution, intraspecific linkage map of pepper (Capsicum annuum L.) was constructed from a population of 297 recombinant inbred lines. The parents were the large-fruited inbred cultivar 'Yolo Wonder' and the hot pepper line 'Criollo de Morelos 334', which is heavily used as a source of resistance to a number of diseases. A set of 587 markers (507 amplified fragment length polymorphisms, 40 simple sequence repeats, 19 restriction fragment length polymorphisms, 17 sequence-specific amplified polymorphisms, and 4 sequence tagged sites) were used to generate the map; of these, 489 were assembled into 49 linkage groups (LGs), including 14 LGs with 10 to 60 markers per LG and 35 with 2 to 9 markers per LG. The framework map covered 1857 cM with an average intermarker distance of 5.71 cM. Twenty-three LGs, composed of 69% of the markers and covering 1553 cM, were assigned to 1 of the 12 haploid pepper chromosomes, leaving 26 LGs (304 cM) unassigned. The chromosome framework map built with 250 markers led to a high level of mapping confidence and an average intermarker distance of 6.54 cM. By applying MapPop software, it was possible to select smaller subsets of 141 or 93 most informative individuals with a view to reducing the time and cost of further mapping and phenotyping. To define the smallest number of individuals sufficient for assigning any new marker to a chromosome, subsets from 12 to 45 individuals and a set of 13 markers distributed over all 12 chromosomes were screened. In most cases, the markers were correctly assigned to their expected chromosome, but the accuracy of the map position decreased as the number of individuals was reduced.
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AFLP: a new technique for DNA fingerprinting
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Rapid Flow Cytometric Analysis of the Cell Cycle in Intact Plant Tissues
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