Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/31
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dc.contributor.authorStummer, B.-
dc.contributor.authorScott, E.-
dc.date.issued2003-
dc.identifier.citationAustralasian Plant Pathology, 2003; 32(2):213-218-
dc.identifier.issn0815-3191-
dc.identifier.issn1448-6032-
dc.identifier.urihttp://hdl.handle.net/2440/31-
dc.description.abstractSexual recombination and segregation in 18 ascospore progeny of Uncinula necator were analysed by mating type (Mat locus), RFLP and PCR markers. Progeny were analysed from a cross of parental isolates representing the genetically distinct phenetic Groups I (AHd2) and II (BNb2). A total of 27 markers was analysed, consisting of four single loci (Mat locus and three RFLP probes), 16 multi-loci (three multi-copy fingerprinting probes) and seven PCR loci. Novel hybrid genotypes were detected in 28 % of the ascospore-derived progeny using the multi-copy RFLP probes, pUn122-11 and pUnP27, and the PCR primers (CAC)₅ and R1, confirming that recombination can occur between isolates representative of the two phenetic groups. This study provides evidence that out-crossing between isolates of U. necator generates novel genotypes and, as such, may have important implications for disease management practices, such as the durability of fungicides and host resistance.-
dc.language.isoen-
dc.publisherCSIRO Publishing-
dc.source.urihttp://dx.doi.org/10.1071/ap03002-
dc.subjectGrapevine powdery mildew-
dc.subjectrecombination-
dc.subjectgenetic analysis-
dc.subjectRFLP and PCR markers-
dc.titleDetection of novel genotypes in progeny from a controlled cross between isolates of Uncinula necator belonging to distinct phenetic groups-
dc.typeJournal article-
dc.identifier.doi10.1071/AP03002-
pubs.publication-statusPublished-
dc.identifier.orcidScott, E. [0000-0001-6829-519X]-
Appears in Collections:Agriculture, Food and Wine publications
Aurora harvest 2

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