The bZIP Transcription Factor Rca1p Is a Central Regulator of a Novel CO2 Sensing Pathway in Yeast
Author(s) -
Fabien Cottier,
Martine Raymond,
Oliver Kurzai,
M. Bolstad,
Worraag Leewattanapasuk,
Claudia Jiménez-López,
Michael Lorenz,
Dominique Sanglard,
Libuše Váchová,
Norman Pavelka,
Zdena Palková,
Fritz A. Mühlschlegel
Publication year - 2012
Publication title -
plos pathogens
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.719
H-Index - 206
eISSN - 1553-7374
pISSN - 1553-7366
DOI - 10.1371/journal.ppat.1002485
Subject(s) - adenylyl cyclase , transcription factor , biology , regulator , microbiology and biotechnology , candida albicans , saccharomyces cerevisiae , yeast , camp dependent pathway , response regulator , signal transduction , transcriptional regulation , biochemistry , genetics , gene , mutant
Like many organisms the fungal pathogen Candida albicans senses changes in the environmental CO 2 concentration. This response involves two major proteins: adenylyl cyclase and carbonic anhydrase (CA). Here, we demonstrate that CA expression is tightly controlled by the availability of CO 2 and identify the bZIP transcription factor Rca1p as the first CO 2 regulator of CA expression in yeast. We show that Rca1p upregulates CA expression during contact with mammalian phagocytes and demonstrate that serine 124 is critical for Rca1p signaling, which occurs independently of adenylyl cyclase. ChIP-chip analysis and the identification of Rca1p orthologs in the model yeast Saccharomyces cerevisiae (Cst6p) point to the broad significance of this novel pathway in fungi. By using advanced microscopy we visualize for the first time the impact of CO 2 build-up on gene expression in entire fungal populations with an exceptional level of detail. Our results present the bZIP protein Rca1p as the first fungal regulator of carbonic anhydrase, and reveal the existence of an adenylyl cyclase independent CO 2 sensing pathway in yeast. Rca1p appears to regulate cellular metabolism in response to CO 2 availability in environments as diverse as the phagosome, yeast communities or liquid culture.
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