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Reference - PMID:9287302 - Isolation, expression, and regulation of the pgr1(+) gene encoding glutathione reductase absolutely required for the growth of Schizosaccharomyces pombe.

Reference summary

PubMed ID
PMID:9287302
Title
Isolation, expression, and regulation of the pgr1(+) gene encoding glutathione reductase absolutely required for the growth of Schizosaccharomyces pombe.
Authors
Lee J, Dawes IW, Roe JH
Citation
J Biol Chem 1997 Sep 12;272(37):23042-9
Publication year
1997
Abstract
The pgr1(+) gene encoding glutathione reductase (GR, EC 1.6.4.2) was isolated from Schizosaccharomyces pombe using a polymerase chain reaction fragment as a probe. The gene consists of two exons and an intron of 55 nucleotides, encoding a polypeptide of 465 amino acids (50,238 Da) with conserved residues characteristic of GR. The transcriptional start site was localized at 239 nucleotides upstream from the ATG initiation codon. The level of transcript as well as the GR enzyme activity increased more than 11-fold when the cloned pgr1(+) gene was expressed on a multicopy plasmid. This overexpression conferred on S. pombe cells more resistance against menadione, a redox cycling agent, but not against H2O2. The level of pgr1(+) transcripts increased by treatment with oxidants such as menadione, cumene hydroperoxide, and diamide. It also increased by treatment with high osmolarity, heat shock, or at the stationary growth phase. The deletion of the pap1(+) gene encoding an AP-1 homolog in S. pombe caused reduction in the pgr1(+) gene expression. Furthermore, Deltapap1 cells lost the inducibility of pgr1(+) gene expression by the above stresses, implying that Pap1 is involved in general stress-inducible gene expression. When the pgr1(+) gene was disrupted, the haploid spores were not viable. Repression of nmt1 promoter-driven pgr1(+) expression by thiamine caused cessation of growth, which was rescued by the episomal pgr1(+) gene. These results indicate that GR activity, which efficiently reduces GSSG, is essentially required for the growth of S. pombe, unlike in Saccharomyces cerevisiae or Escherichia coli.

Annotation

GO biological process

GO:0098869 - cellular oxidant detoxification

Genes:

GO:0006749 - glutathione metabolic process

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GO:0070301 - cellular response to hydrogen peroxide

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GO molecular function

GO:0004362 - glutathione-disulfide reductase (NADPH) activity

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Qualitative gene expression

PomGeneEx:0000011 - RNA level increased

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PomGeneEx:0000013 - RNA level unchanged

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PomGeneEx:0000014 - RNA present

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Single locus phenotype

FYPO:0001107 - decreased glutathione-disulfide reductase activity

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Genotypes:

FYPO:0000826 - decreased RNA level

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Genotypes:

FYPO:0001111 - increased cellular glutathione disulfide level

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Genotypes:

FYPO:0001108 - increased glutathione-disulfide reductase activity

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Genotypes:

FYPO:0000825 - increased RNA level during vegetative growth

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Genotypes:

FYPO:0001110 - inviable after spore germination, multiple cell divisions, normal morphology

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Genotypes:

FYPO:0002061 - inviable vegetative cell population

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FYPO:0000962 - normal growth on hydrogen peroxide

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Genotypes:

FYPO:0001109 - resistance to menadione

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Genotypes: