Coregulated expression of the Na+/phosphate Pho89 transporter and Ena1 Na+-ATPase allows their functional coupling under high-pH stress

Mol Cell Biol. 2014 Dec;34(24):4420-35. doi: 10.1128/MCB.01089-14. Epub 2014 Sep 29.

Abstract

The yeast Saccharomyces cerevisiae has two main high-affinity inorganic phosphate (Pi) transporters, Pho84 and Pho89, that are functionally relevant at acidic/neutral pH and alkaline pH, respectively. Upon Pi starvation, PHO84 and PHO89 are induced by the activation of the PHO regulon by the binding of the Pho4 transcription factor to specific promoter sequences. We show that PHO89 and PHO84 are induced by alkalinization of the medium with different kinetics and that the network controlling Pho89 expression in response to alkaline pH differs from that of other members of the PHO regulon. In addition to Pho4, the PHO89 promoter is regulated by the transcriptional activator Crz1 through the calcium-activated phosphatase calcineurin, and it is under the control of several repressors (Mig2, Nrg1, and Nrg2) coordinately regulated by the Snf1 protein kinase and the Rim101 transcription factor. This network mimics the one regulating expression of the Na(+)-ATPase gene ENA1, encoding a major determinant for Na(+) detoxification. Our data highlight a scenario in which the activities of Pho89 and Ena1 are functionally coordinated to sustain growth in an alkaline environment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcineurin / metabolism
  • Culture Media / chemistry
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Gene Expression Regulation, Fungal*
  • Genome, Fungal
  • Hydrogen-Ion Concentration
  • Phosphates / metabolism
  • Promoter Regions, Genetic
  • Proton-Phosphate Symporters / genetics
  • Proton-Phosphate Symporters / metabolism*
  • Repressor Proteins / metabolism
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae / physiology*
  • Saccharomyces cerevisiae Proteins / genetics*
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Signal Transduction
  • Sodium-Phosphate Cotransporter Proteins, Type III / genetics*
  • Sodium-Phosphate Cotransporter Proteins, Type III / metabolism*
  • Sodium-Potassium-Exchanging ATPase / genetics
  • Sodium-Potassium-Exchanging ATPase / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • CRZ1 protein, S cerevisiae
  • Culture Media
  • DNA-Binding Proteins
  • ENA1 protein, S cerevisiae
  • PHO4 protein, S cerevisiae
  • PHO84 protein, S cerevisiae
  • PHO89 protein, S cerevisiae
  • Phosphates
  • Proton-Phosphate Symporters
  • Repressor Proteins
  • Saccharomyces cerevisiae Proteins
  • Sodium-Phosphate Cotransporter Proteins, Type III
  • Transcription Factors
  • Calcineurin
  • Sodium-Potassium-Exchanging ATPase