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DAF marker tightly linked to a major locus for Ascochyta blight resistance in chickpea (Cicer arietinum L.)
Authors:S Rakshit  P Winter  M Tekeoglu  J Juarez Muñoz  T Pfaff  A-M Benko-Iseppon  FJ Muehlbauer  G Kahl
Institution:(1) Indian Institute of Pulses Research, Kanpur, 208024, India;(2) Plant Molecular Biology, Biocentre, University of Frankfurt, D-60439 Frankfurt, Germany;(3) Colegio de Posgraduados, Montecillo, Edo. de Mexico, 56230, Mexico;(4) Universidade Federal de Pernambuco, UFPE, CCB, Genética, Recife – PE, Brazil;(5) Grain Legume Genetics and Physiology Research Unit, U.S. Department of Agriculture, Agricultural Research Service and Department of Crop and Soil Sciences, 303 Johnson Hall, Washington State University, Pullman, WA, 99164-6434, U.S.A
Abstract:Resistance of chickpea against the disease caused by the ascomycete Ascochyta rabiei is encoded by two or three quantitative trait loci, QTL1, QTL2 and QTL3. A total of 94 recombinant inbred lines developed from a wide cross between a resistant chickpea line and a susceptible accession of Cicer reticulatum, a close relative of cultivated chickpea, was used to identify markers closely linked to QTL1 by DNA amplification fingerprinting in combination with bulked segregant analysis. Of 312 random 10mer oligonucleotides, 3 produced five polymorphic bands between the parents and bulks. Two of them were transferred to the population on which the recent genetic map of chickpea is based, and mapped to linkage group 4. These markers, OPS06-1 and OPS03-1, were linked at LOD-scores above 5 to markers UBC733B and UBC181A flanking the major ascochyta resistance locus. OPS06-1 mapped at the peak of the QTL between markers UBC733B (distance 4.1 cM) and UBC181A (distance 9.6 cM), while OPS03-1 mapped 25.1 cM away from marker UBC733B on the other flank of the resistance locus. STMS markers localised on this linkage group were transferred to the population segregating for ascochyta resistance. Three of these markers were closely linked to QTL1. Twelve of 14 STMS markers could be used in both populations. The order of STMS markers was essentially similar in both populations, with differences in map distances between them. The availability of flanking STMS markers for the major resistance locus QTL1 will help to elucidate the complex resistance against different Ascochyta pathotypes in future. This revised version was published online in August 2006 with corrections to the Cover Date.
Keywords:Ascochyta rabiei            chickpea  disease resistance  DNAamplification fingerprinting  genetic map
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