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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Integrated pest management reviews 1 (1996), S. 191-200 
    ISSN: 1572-9745
    Keywords: Phaseolus vulgaris ; durable host resistance ; Uromyces appendiculatus ; bean rust ; integrated disease management ; common bean ; partial resistance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Bean rust, caused by Uramyces appendiculatus, is one of the major diseases in dry and snap bean production world-wide. Numerous advancements in disease management have been made to reduce rust losses. Host resistance is an important component of rust management. However, durability of disease resistance has often been short due to the use of single genes for resistance interacting with extremely high virulence diversity of the bean rust fungus. The challenge to increase durability of resistance has led to strategies such as gene pyramiding of race-specific resistance, selection and use of partial resistance, and investigation and discovery of leaf morphological features that may slow the rust epidemic. Germplasm with multiple sources of rust resistance has been developed in specific bean seed classes and released for public and commercial use in intensive production systems such as those in the United States. However, progress to develop rust resistant germplasm for the subsistence agriculture of Latin America and Africa where intercropping and mixed cultivars dominate the production system has been slow. Incorporation of high yielding, disease-resistant components as partial replacement in farmer's mixtures has the potential to reduce severity in the crop and increase yield in the presence of rust. This strategy would not erode the genetic diversity that is historically known to enhance resistance durability and for many years has given stability in production in the subsistent agriculture systems.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 85 (1993), S. 745-749 
    ISSN: 1432-2242
    Keywords: Polymerase chain reaction ; Random amplified polymorphic DNA (RAPD) ; Phaseolus vulgaris ; Uromyces appendiculatus ; Gene pyramiding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The Up 2 gene of common bean (Phaseolus Vulgaris L.) is an important source of dominant genetic resistance to the bean rust pathogen [Uromyces appendiculatus (Pers. ex Pers.) Unger var ‘appendiculatus’ [syn U. Phaseoli (Reben) Wint.]. Up 2 in combination with other rust resistance genes may be used to obtain potentially stable genetic resistance. It is difficult, however, to combine rust resistance genes effective against a single race due to epistatic interactions that frequently occur between them. A strategy that employed bulked DNA samples formed separately from the DNA of three BC6F2 individuals with Up 2 and three without Up 2 as contrasting near-isogenic lines (NILs) was used to identify random amplified polymorphic DNA fragments (RAPDs) tightly linked to the Up 2 locus. Only 1 of 931 fragments amplified by 167 10-mer primers of arbitrary sequence in the polymerase chain reaction (PCR) was polymorphic. The RAPD marker (OA141100) amplified by the 5′-TCTGTGCTGG-3′ primer was repeatable and its presence and absence easy to score. No recombination was observed between OA141100 and the dominant Up 2 allele within a segregating BC6F2 population of 84 individuals. This result suggests that OA141100 and Up 2 are tightly linked. Andean and Mesoamerican bean germ plasm, with and without the Up 2 allele, were assayed for the presence of OA141100. Apparently, the marker is of Andean origin because all Andean lines, with or without the Up 2 allele, contained the marker, and the marker was absent in all Mesoamerican germ plasm except the lines to which Up-2 had been purposely transferred. These results suggest that OA141100 will be most useful for pyramiding Up 2 with other rust resistance genes into germ plasm of Mesoamerican origin where the marker does not traditionally exist. The use of bulked DNA samples may have concentrated resources toward the identification of RAPDs that were tightly linked to the target locus. Marker-based selection may provide an alternative to the time-consuming testcrosses required to pyramid bean rust resistance genes that exhibit epistasis.
    Type of Medium: Electronic Resource
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