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• W1554794322 startingPage "4342" @default.
• W1554794322 abstract "We have identified a cell surface ferric reductase activity in the fission yeast Schizosaccharomyces pombe. A mutant strain deficient in this activity was also deficient in ferric iron uptake, while ferrous iron uptake was not impaired. Therefore, reduction is a required step in cellular ferric iron acquisition. We have cloned frp1+, the wild-type allele of the mutant gene. frp1+ mRNA levels were repressed by iron addition to the growth medium. Fusion of 138 nucleotides of frp1+ promoter sequences to a reporter gene, the bacterial chloramphenicol acetyltransferase gene, conferred iron-dependent regulation upon the latter when introduced into S. pombe. The predicted amino acid sequence of the frp1+ gene exhibits hydrophobic regions compatible with transmembrane domains. It shows similarity to the Saccharomyces cerevisiae FRE1 gene product and the gp91-phox protein, a component of the human NADPH phagocyte oxidoreductase that is deficient in X-linked chronic granulomatous disease." @default.
• W1554794322 created "2016-06-24" @default.
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• W1554794322 date "1993-07-01" @default.
• W1554794322 modified "2023-09-25" @default.
• W1554794322 title "The fission yeast ferric reductase gene frp1+ is required for ferric iron uptake and encodes a protein that is homologous to the gp91-phox subunit of the human NADPH phagocyte oxidoreductase." @default.
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• W1554794322 doi "https://doi.org/10.1128/mcb.13.7.4342" @default.
• W1554794322 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/359993" @default.
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