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Reference - PMID:24569997 - Characterization of Schizosaccharomyces pombe copper transporter proteins in meiotic and sporulating cells.

Reference summary

PubMed ID
PMID:24569997
Title
Characterization of Schizosaccharomyces pombe copper transporter proteins in meiotic and sporulating cells.
Authors
Plante S, Ioannoni R, Beaudoin J, Labbé S
Citation
J Biol Chem 2014 Apr 04;289(14):10168-81
Publication year
2014
Abstract
Meiosis requires copper to undertake its program in which haploid gametes are produced from diploid precursor cells. In Schizosaccharomyces pombe, copper is transported by three members of the copper transporter (Ctr) family, namely Ctr4, Ctr5, and Ctr6. Although central for sexual differentiation, very little is known about the expression profile, cellular localization, and physiological contribution of the Ctr proteins during meiosis. Analysis of gene expression of ctr4(+) and ctr5(+) revealed that they are primarily expressed in early meiosis under low copper conditions. In the case of ctr6(+), its expression is broader, being detected throughout the entire meiotic process with an increase during middle- and late-phase meiosis. Whereas the expression of ctr4(+) and ctr5(+) is exclusively dependent on the presence of Cuf1, ctr6(+) gene expression relies on two distinct regulators, Cuf1 and Mei4. Ctr4 and Ctr5 proteins co-localize at the plasma membrane shortly after meiotic induction, whereas Ctr6 is located on the membrane of vacuoles. After meiotic divisions, Ctr4 and Ctr5 disappear from the cell surface, whereas Ctr6 undergoes an intracellular re-location to co-localize with the forespore membrane. Under copper-limiting conditions, disruption of ctr4(+) and ctr6(+) results in altered SOD1 activity, whereas these mutant cells exhibit substantially decreased levels of CAO activity mostly in early- and middle-phase meiosis. Collectively, these results emphasize the notion that Ctr proteins exhibit differential expression, localization, and contribution in delivering copper to SOD1 and Cao1 proteins during meiosis.

Annotation

GO cellular component

GO:0000329 - fungal-type vacuole membrane

Genes:

GO:0005886 - plasma membrane

Genes:

GO:0005628 - prospore membrane

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GO molecular function

GO:0001228 - DNA-binding transcription activator activity, RNA polymerase II-specific

Genes:

Multi-locus phenotype

FYPO:0003073 - decreased primary amine oxidase activity

Genes:

Genotypes:

FYPO:0006145 - decreased RNA level during cellular response to copper ion during meiotic cell cycle

Genes:

Genotypes:

FYPO:0006170 - decreased RNA level during cellular response to copper ion starvation during meiotic cell cycle

Genes:

Genotypes:

FYPO:0003282 - decreased superoxide dismutase activity

Genes:

Genotypes:

Qualitative gene expression

PomGeneEx:0000011 - RNA level increased

Genes:

PomGeneEx:0000014 - RNA present

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Single locus phenotype

FYPO:0004039 - abolished primary amine oxidase activity

Genes:

Genotypes:

FYPO:0006147 - decreased level of early meiotic gene mRNA during cellular response to copper ion starvation during meiotic cell cycle

Genes:

Genotypes:

FYPO:0003073 - decreased primary amine oxidase activity

Genes:

Genotypes:

FYPO:0006145 - decreased RNA level during cellular response to copper ion during meiotic cell cycle

Genes:

Genotypes:

FYPO:0006170 - decreased RNA level during cellular response to copper ion starvation during meiotic cell cycle

Genes:

Genotypes:

FYPO:0003282 - decreased superoxide dismutase activity

Genes:

Genotypes:

FYPO:0006146 - normal RNA level during cellular response to copper ion starvation during meiotic cell cycle

Genes:

Genotypes: