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• W2108941919 startingPage "e43208" @default.
• W2108941919 abstract "Arsenic toxicity has been studied for a long time due to its effects in humans. Although epidemiological studies have demonstrated multiple effects in human physiology, there are many open questions about the cellular targets and the mechanisms of response to arsenic. Using the fission yeast Schizosaccharomyces pombe as model system, we have been able to demonstrate a strong activation of the MAPK Spc1/Sty1 in response to arsenate. This activation is dependent on Wis1 activation and Pyp2 phosphatase inactivation. Using arsenic speciation analysis we have also demonstrated the previously unknown capacity of S. pombe cells to reduce As (V) to As (III). Genetic analysis of several fission yeast mutants point towards the cell cycle phosphatase Cdc25 as a possible candidate to carry out this arsenate reductase activity. We propose that arsenate reduction and intracellular accumulation of arsenite are the key mechanisms of arsenate tolerance in fission yeast." @default.
• W2108941919 created "2016-06-24" @default.
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• W2108941919 date "2012-08-17" @default.
• W2108941919 modified "2023-10-05" @default.
• W2108941919 title "Response to Arsenate Treatment in Schizosaccharomyces pombe and the Role of Its Arsenate Reductase Activity" @default.
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• W2108941919 doi "https://doi.org/10.1371/journal.pone.0043208" @default.
• W2108941919 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3422283" @default.
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• W2108941919 hasPublicationYear "2012" @default.
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