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Construction of a BAC library and a physical map of a major QTL for CBB resistance of common bean (<Emphasis Type="Italic">Phaseolus vulgaris</Emphasis> L.)
Authors:S Y Liu  K Yu  M Huffner  S J Park  M Banik  K P Pauls  W Crosby
Institution:(1) Agriculture Agri-Food Canada, Greenhouse and Processing Crops Research Center, Harrow, ON, N0R 1G0, Canada;(2) Department of Plant Agriculture, Crop Science Building, University of Guelph, Guelph, ON, N1G 2W1, Canada;(3) Present address: Crop and Soil Environmental Science, Virginia Polytechnic Institute and State University, Blacksburg, VA 24060, USA;(4) Present address: Cereal Research Center, Agriculture and Agri-Food Canada, Winnipeg, MB, R3T 2M9, Canada;(5) Department of Biology, University of Windsor, Windsor, ON, N9B 3P4, Canada;
Abstract:A major quantitative trait loci (QTL) conditioning common bacterial blight (CBB) resistance in common bean (Phaseolus vulgaris L.) lines HR45 and HR67 was derived from XAN159, a resistant line obtained from an interspecific cross between common bean lines and the tepary bean (P. acutifolius L.) line PI319443. This source of CBB resistance is widely used in bean breeding. Several other CBB resistance QTL have been identified but none of them have been physically mapped. Four molecular markers tightly linked to this QTL have been identified suitable for marker assisted selection and physical mapping of the resistance gene. A bacterial artificial chromosome (BAC) library was constructed from high molecular weight DNA of HR45 and is composed of 33,024 clones. The size of individual BAC clone inserts ranges from 30 kb to 280 kb with an average size of 107 kb. The library is estimated to represent approximately sixfold genome coverage. The BAC library was screened as BAC pools using four PCR-based molecular markers. Two to seven BAC clones were identified by each marker. Two clones were found to have both markers PV-tttc001 and STS183. One preliminary contig was assembled based on DNA finger printing of those positive BAC clones. The minimum tiling path of the contig contains 6 BAC clones spanning an estimated size of 750 kb covering the QTL region.
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