DNA fingerprinting of Ascochyta rabiei with synthetic oligodeoxynucleotides

cg.contactM.SAXENA@CGIAR.ORGen_US
cg.contributor.centerInternational Center for Agricultural Research in the Dry Areas - ICARDAen_US
cg.contributor.centerGoethe University-Frankfurt - GU-Frankfurten_US
cg.contributor.centerMax Planck Institute of Psychiatryen_US
cg.contributor.funderInternational Center for Agricultural Research in the Dry Areas - ICARDAen_US
cg.contributor.projectCommunication and Documentation Information Services (CODIS)en_US
cg.contributor.project-lead-instituteInternational Center for Agricultural Research in the Dry Areas - ICARDAen_US
cg.date.embargo-end-dateTimelessen_US
cg.identifier.doihttps://dx.doi.org/10.1007/BF00312740en_US
cg.isijournalISI Journalen_US
cg.issn0172-8083en_US
cg.journalCurrent Geneticsen_US
cg.subject.agrovocdna fingerprintingen_US
cg.subject.agrovocChickpeaen_US
cg.volume19en_US
dc.contributorKaemmer, Dieteren_US
dc.contributorEpplen, Jörg T.en_US
dc.contributorWeigand, Franzen_US
dc.contributorSaxena, Mohan C.en_US
dc.contributorKahl, Günteren_US
dc.creatorWeising, Kurten_US
dc.date.accessioned2020-12-02T19:55:04Z
dc.date.available2020-12-02T19:55:04Z
dc.description.abstractThe ascomycete fungus Ascochyta rabiei, an important pathogen of the grain legume crop chickpea (Cicer arietinum L.) in the Mediterranean region, has not been adequately characterized in molecular terms. We therefore used DNA fingerprinting, with synthetic oligodeoxynucleotides complementary to simple repetitive sequences, to pathotype different isolates of the fungus. Six single-spored A. rabiei isolates were first categorized using a host differential set of nine chickpea genotypes. Seedlings were inoculated under controlled environmental conditions, and disease severity was recorded 9 days after inoculation. DNA was extracted from in vitro-grown mycelia of the six purified fungal isolates, restricted with EcoRI, HinfI, MboII and TaqI, and fingerprinted with radiolabeled (GATA)4, (GTG)5, (CA)8, and (TCC)5, respectively. High levels of polymorphism were detected with optimal enzyme/probe combinations that allow one to discriminate between the isolates. The potential of DNA fingerprinting with simple repetitive sequences can thus be expanded to the identification of fungal races and pathotypes. The characterization of the geographic distribution and genetic variability of pathotypes will facilitate the selection of suitable host cultivars to be grown in specific regions.en_US
dc.identifierhttps://mel.cgiar.org/dspace/limiteden_US
dc.identifier.citationKurt Weising, Dieter Kaemmer, Jörg T. Epplen, Franz Weigand, Mohan C. Saxena, Günter Kahl. (1/6/1991). DNA fingerprinting of Ascochyta rabiei with synthetic oligodeoxynucleotides. Current Genetics, 19, pp. 483-489.en_US
dc.identifier.statusTimeless limited accessen_US
dc.identifier.urihttps://hdl.handle.net/20.500.11766/12139
dc.languageenen_US
dc.publisherSpringeren_US
dc.sourceCurrent Genetics;19,(1991) Pagination 483-489en_US
dc.subjectsynthetic oligodeoxynucleotidesen_US
dc.subjectsimple repetitive sequencesen_US
dc.subjectfungal pathotypesen_US
dc.subjectascochyta-rabieien_US
dc.titleDNA fingerprinting of Ascochyta rabiei with synthetic oligodeoxynucleotidesen_US
dc.typeJournal Articleen_US
dcterms.available1991-06-01en_US
dcterms.extent483-489en_US
mel.impact-factor3.464 (2018)en_US

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