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Cloning and genetic analyses of two highly polymorphic,moderately repetitive nuclear DNAs from Phytophthora infestans
Authors:Stephen B. Goodwin  André Drenth  William E. Fry
Affiliation:(1) Department of Plant Pathology, 334 Plant Science, Cornell University, 14853 Ithaca, NY, USA;(2) Present address: Department of Phytopathology, Wageningen Agricultural University, P.O. Box 8025, NL-6700 EE Wageningen, The Netherlands
Abstract:Summary Randomly selected clones from a Phytophthora infestans partial genomic library were characterized by hybridizing individual clones to Southern blots of total genomic DNA digested with the restriction enzyme EcoRI. Among 59 clones that were screened on seven different central-Mexican isolates, five revealed a unique banding pattern for each isolate tested. Two of these clones were tested further; the banding patterns produced by both were somatically stable when probed to DNA from 63 single-zoospore (asexual) progeny from five different ldquoparentrdquo isolates. For one probe, RG57, each band appeared to represent a unique genetic locus in three different crosses, and each locus segregated for the presence or absence of a band. No bands were found to be allelic, but two pairs of cosegregating loci were identified. Genetic analyses of the other probe (RG7) revealed many more pairs of cosegregating bands and some bands which were allelic. When these probes were hybridized to DNA from the other five species in Phytophthora group IV, probe RG57 hybridized strongly to DNA from P. colocasiae, P. phaseoli and P. mirabilis, but weakly or not at all to that of P. hibernalis and P. ilicis. Probe RG7 hybridized fairly strongly to DNA from all six species. Because the sequence recognized by probe RG57 appears to be evolutionarily conserved, and is dispersed, moderately repetitive and highly polymorphic, it could be very useful in additional studies on the genetics and population biology of P. infestans.
Keywords:DNA fingerprinting  Phytophthora  Genetic analysis  Molecular markers
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