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Marker construction and cloning of a cut1-like sequence with ARS activity in the fission yeast Schizosaccharomyces japonicus.
Bozsik, Aniko; Szilagyi, Z; Benko, Z; Sipiczki, M.
Afiliação
  • Bozsik A; Department of Genetics, University of Debrecen, Debrecen, Hungary.
Yeast ; 19(6): 485-98, 2002 Apr.
Article em En | MEDLINE | ID: mdl-11921097
The dimorphic fission yeast Schizosaccharomyces japonicus has proved to be an excellent experimental model for the investigation of the eukaryotic cell. Here we show that it has a haplontic life cycle, in which the diploid phase is confined to the zygote. To make it amenable to genetic and molecular analysis, we generated genetic markers and cloned a genomic sequence which acts as ars when integrated into a plasmid. Diploids suitable for testing complementation and recombination between markers can be formed by protoplast fusion. The complementation tests and the recombination frequencies determined in octads of spores identified 28 non-allelic groups (genes) of mutations of the auxotrophic and mycelium-negative mutants. Two groups of linked markers were also identified. The cloned fragment, which expresses ars activity, encodes a putative amino acid sequence highly similar to a conserved domain of proteins Cut1 (Schizosaccharomyces pombe), BimB (Aspergillus nidulans) and Esp1 (Saccharomyces cerevisiae).
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Schizosaccharomyces / DNA Fúngico / Proteínas de Ciclo Celular / Proteínas de Schizosaccharomyces pombe / Replicação do DNA Idioma: En Revista: Yeast Assunto da revista: MICROBIOLOGIA Ano de publicação: 2002 Tipo de documento: Article País de afiliação: Hungria País de publicação: Reino Unido
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Schizosaccharomyces / DNA Fúngico / Proteínas de Ciclo Celular / Proteínas de Schizosaccharomyces pombe / Replicação do DNA Idioma: En Revista: Yeast Assunto da revista: MICROBIOLOGIA Ano de publicação: 2002 Tipo de documento: Article País de afiliação: Hungria País de publicação: Reino Unido