The use of RAPD markers in the genetic analysis of the plant pathogenic fungus Cladosporium fulvum

RAPD markers have been obtained in Cladosporium fulvum, in order to establish a genetic map based on mitotic recombination in this imperfect fungus. Segregation analysis has provided molecular evidence of a high degree of recombination during the parasexual cycle, and of the ploidy level of the para...

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Main Authors: Arnau, J., Oliver, Richard
Format: Journal Article
Published: 1994
Online Access:http://hdl.handle.net/20.500.11937/30438
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author Arnau, J.
Oliver, Richard
author_facet Arnau, J.
Oliver, Richard
author_sort Arnau, J.
building Curtin Institutional Repository
collection Online Access
description RAPD markers have been obtained in Cladosporium fulvum, in order to establish a genetic map based on mitotic recombination in this imperfect fungus. Segregation analysis has provided molecular evidence of a high degree of recombination during the parasexual cycle, and of the ploidy level of the parasexual progeny. A molecular study of 49 RAPDs obtained showed that, with only one exception, all RAPD markers studied represent repetitive DNA. This situation precludes the direct use of these markers to either initiate chromosome walking to a gene of interest or for the assignment of linkage groups to electrophoretically-separated chromosomes. A simple reamplification test has been applied which permitted the quick discrimination between single-copy and repetitive DNA species, without the need for Southern analysis. Additionally, evidence is shown for the presence of single-stranded DNA species in the amplification products, and that these may be present in addition to their double-stranded counterparts. The reamplification test can also identify these DNA species, avoiding misinterpretation of polymorphic bands.
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publishDate 1994
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spelling curtin-20.500.11937-304382017-09-13T16:08:47Z The use of RAPD markers in the genetic analysis of the plant pathogenic fungus Cladosporium fulvum Arnau, J. Oliver, Richard RAPD markers have been obtained in Cladosporium fulvum, in order to establish a genetic map based on mitotic recombination in this imperfect fungus. Segregation analysis has provided molecular evidence of a high degree of recombination during the parasexual cycle, and of the ploidy level of the parasexual progeny. A molecular study of 49 RAPDs obtained showed that, with only one exception, all RAPD markers studied represent repetitive DNA. This situation precludes the direct use of these markers to either initiate chromosome walking to a gene of interest or for the assignment of linkage groups to electrophoretically-separated chromosomes. A simple reamplification test has been applied which permitted the quick discrimination between single-copy and repetitive DNA species, without the need for Southern analysis. Additionally, evidence is shown for the presence of single-stranded DNA species in the amplification products, and that these may be present in addition to their double-stranded counterparts. The reamplification test can also identify these DNA species, avoiding misinterpretation of polymorphic bands. 1994 Journal Article http://hdl.handle.net/20.500.11937/30438 10.1007/BF00351783 restricted
spellingShingle Arnau, J.
Oliver, Richard
The use of RAPD markers in the genetic analysis of the plant pathogenic fungus Cladosporium fulvum
title The use of RAPD markers in the genetic analysis of the plant pathogenic fungus Cladosporium fulvum
title_full The use of RAPD markers in the genetic analysis of the plant pathogenic fungus Cladosporium fulvum
title_fullStr The use of RAPD markers in the genetic analysis of the plant pathogenic fungus Cladosporium fulvum
title_full_unstemmed The use of RAPD markers in the genetic analysis of the plant pathogenic fungus Cladosporium fulvum
title_short The use of RAPD markers in the genetic analysis of the plant pathogenic fungus Cladosporium fulvum
title_sort use of rapd markers in the genetic analysis of the plant pathogenic fungus cladosporium fulvum
url http://hdl.handle.net/20.500.11937/30438