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Yeast
Article . 1998 . Peer-reviewed
License: Wiley TDM
Data sources: Crossref
Yeast
Article . 1998
versions View all 4 versions

Disruption of sixSaccharomyces cerevisiae genes from chromosome IV and basic phenotypic analysis of deletion mutants

Authors: López, M. Carmen; Sánchez, Manuel; Fermiñán, Encarnación; Domínguez Olavarri, Ángel;

Disruption of sixSaccharomyces cerevisiae genes from chromosome IV and basic phenotypic analysis of deletion mutants

Abstract

We report here the construction of six deletion mutants and the analysis of their basic phenotype. Deletion cassettes containing the KanMX4 marker module and long flanking regions homologous to the target locus were constructed for each of the six open reading-frames (ORFs YDL088c, YDL087c, YDL086w, YDL085w, YDL084w and YDL082w) located on chromosome IV. Sporulation and tetrad analysis of heterozygous deletant strains revealed that, in the FY1679 genetic background, ORFs YDL088c, YDL087c and YDL084w are essential genes for vegetative growth whereas YDL086w, YDL085w and YDL082w are non-essential. ydl088c delta and ydl084w delta haploid strains are viable in the CEN. PK2 genetic background although ydl084w delta grows at a slower rate than the wild type. Complementation tests by corresponding cognate genes confirmed that gene inactivation was responsible for these growth defects.

Keywords

Genes, Fungal, Genetic Complementation Test, Saccharomyces cerevisiae, Spores, Fungal, Polymerase Chain Reaction, Mutagenesis, Insertional, Open Reading Frames, Phenotype, Kanamycin, Escherichia coli, Cloning, Molecular, Gene Deletion

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popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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