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Paxilline-negative mutants of Penicillium paxilli generated by heterologous and homologous plasmid integration
Authors:Carolyn Young  Yasuo Itoh  R. Johnson  I. Garthwaite  Christopher O. Miles  Sarah C. Munday-Finch  B. Scott
Affiliation:(1) Institute of Molecular BioSciences, Massey University, Palmerston North, New Zealand Fax: +64-6-350 5637 e-mail: d.b.scott@massey.ac.nz, NZ;(2) Department of Biology, Shinshu University, Matsumoto, Nagano, 390 Japan, JP;(3) Ruakura Agricultural Research Centre, AgResearch, Hamilton, New Zealand, NZ
Abstract:Using a monoclonal antibody based ELISA, 600 pAN7-1 plasmid-tagged mutants of Penicillium paxilli were screened for paxilline accumulation and one paxilline-negative mutant, YI-20, was identified. A molecular analysis of this mutant showed that pAN7-1 was inserted at a single site but was present as 4–6 copies arranged in a head-to-tail tandem array. Rescue of flanking sequences and analysis of the corresponding genomic region revealed that YI-20 has an extensive deletion at the site of pAN7-1 integration. Probing of a CHEF gel with the same sequences showed that associated with the deletion is a rearrangement of chromosome Va. Targeted gene disruption of wild-type sequences adjacent to the site where pAN7-1 inserted, resulted in the generation of two additional paxilline-negative mutants; both were single crossovers with deletions extending outside the region mapped. Neither of these new mutants had a rearrangement of chromosome Va, suggesting that deletion of genes on this chromosome is responsible for the paxilline-negative phenotype. Telomeric fingerprinting of genomic digests of P. paxilli, combined with pulsed-field gel electrophoresis of chromosomal DNA, established that there are a minimum of eight chromosomes in this fungus. Received: 5 January / 27 February 1998
Keywords:Penicillium paxilli  Paxilline mutants  Plasmid tagging  Homologous recombination  Deletion mutations  pAN7-1
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