Lipid Signaling via Pkh1/2 Regulates Fungal CO2 Sensing through the Kinase Sch9

Adaptation to alternating CO2 concentrations is crucial for all organisms. Carbonic anhydrases—metalloenzymes that have been found in all domains of life—enable fixation of scarce CO2 by accelerating its conversion to bicarbonate and ensure maintenance of cellular metabolism. In fungi and other euka...

Full description

Bibliographic Details
Main Authors: Susann Pohlers, Ronny Martin, Thomas Kruger, Daniela Hellwig, Frank Hanel, Olaf Kniemeyer, Hans Peter Saluz, Patrick Van Dijck, Joachim F. Ernst, Axel Brakhage, Fritz A. Muhlschlegel, Oliver Kurzai, Michael Lorenz
Format: Article
Language:English
Published: American Society for Microbiology 2017-01-01
Series:mBio
Online Access:http://mbio.asm.org/cgi/content/full/8/1/e02211-16
id doaj-0b1c5282b28a4b0191ee6c0f811cb2cb
record_format Article
spelling doaj-0b1c5282b28a4b0191ee6c0f811cb2cb2021-07-02T01:38:19ZengAmerican Society for MicrobiologymBio2150-75112017-01-0181e02211-1610.1128/mBio.02211-16Lipid Signaling via Pkh1/2 Regulates Fungal CO2 Sensing through the Kinase Sch9Susann PohlersRonny MartinThomas KrugerDaniela HellwigFrank HanelOlaf KniemeyerHans Peter SaluzPatrick Van DijckJoachim F. ErnstAxel BrakhageFritz A. MuhlschlegelOliver KurzaiMichael LorenzAdaptation to alternating CO2 concentrations is crucial for all organisms. Carbonic anhydrases—metalloenzymes that have been found in all domains of life—enable fixation of scarce CO2 by accelerating its conversion to bicarbonate and ensure maintenance of cellular metabolism. In fungi and other eukaryotes, the carbonic anhydrase Nce103 has been shown to be essential for growth in air (~0.04% CO2). Expression of NCE103 is regulated in response to CO2 availability. In Saccharomyces cerevisiae, NCE103 is activated by the transcription factor ScCst6, and in Candida albicans and Candida glabrata, it is activated by its homologues CaRca1 and CgRca1, respectively. To identify the kinase controlling Cst6/Rca1, we screened an S. cerevisiae kinase/phosphatase mutant library for the ability to regulate NCE103 in a CO2-dependent manner. We identified ScSch9 as a potential ScCst6-specific kinase, as the sch9Δ mutant strain showed deregulated NCE103 expression on the RNA and protein levels. Immunoprecipitation revealed the binding capabilities of both proteins, and detection of ScCst6 phosphorylation by ScSch9 in vitro confirmed Sch9 as the Cst6 kinase. We could show that CO2-dependent activation of Sch9, which is part of a kinase cascade, is mediated by lipid/Pkh1/2 signaling but not TORC1. Finally, we tested conservation of the identified regulatory cascade in the pathogenic yeast species C. albicans and C. glabrata. Deletion of SCH9 homologues of both species impaired CO2-dependent regulation of NCE103 expression, which indicates a conservation of the CO2 adaptation mechanism among yeasts. Thus, Sch9 is a Cst6/Rca1 kinase that links CO2 adaptation to lipid signaling via Pkh1/2 in fungi.http://mbio.asm.org/cgi/content/full/8/1/e02211-16
collection DOAJ
language English
format Article
sources DOAJ
author Susann Pohlers
Ronny Martin
Thomas Kruger
Daniela Hellwig
Frank Hanel
Olaf Kniemeyer
Hans Peter Saluz
Patrick Van Dijck
Joachim F. Ernst
Axel Brakhage
Fritz A. Muhlschlegel
Oliver Kurzai
Michael Lorenz
spellingShingle Susann Pohlers
Ronny Martin
Thomas Kruger
Daniela Hellwig
Frank Hanel
Olaf Kniemeyer
Hans Peter Saluz
Patrick Van Dijck
Joachim F. Ernst
Axel Brakhage
Fritz A. Muhlschlegel
Oliver Kurzai
Michael Lorenz
Lipid Signaling via Pkh1/2 Regulates Fungal CO2 Sensing through the Kinase Sch9
mBio
author_facet Susann Pohlers
Ronny Martin
Thomas Kruger
Daniela Hellwig
Frank Hanel
Olaf Kniemeyer
Hans Peter Saluz
Patrick Van Dijck
Joachim F. Ernst
Axel Brakhage
Fritz A. Muhlschlegel
Oliver Kurzai
Michael Lorenz
author_sort Susann Pohlers
title Lipid Signaling via Pkh1/2 Regulates Fungal CO2 Sensing through the Kinase Sch9
title_short Lipid Signaling via Pkh1/2 Regulates Fungal CO2 Sensing through the Kinase Sch9
title_full Lipid Signaling via Pkh1/2 Regulates Fungal CO2 Sensing through the Kinase Sch9
title_fullStr Lipid Signaling via Pkh1/2 Regulates Fungal CO2 Sensing through the Kinase Sch9
title_full_unstemmed Lipid Signaling via Pkh1/2 Regulates Fungal CO2 Sensing through the Kinase Sch9
title_sort lipid signaling via pkh1/2 regulates fungal co2 sensing through the kinase sch9
publisher American Society for Microbiology
series mBio
issn 2150-7511
publishDate 2017-01-01
description Adaptation to alternating CO2 concentrations is crucial for all organisms. Carbonic anhydrases—metalloenzymes that have been found in all domains of life—enable fixation of scarce CO2 by accelerating its conversion to bicarbonate and ensure maintenance of cellular metabolism. In fungi and other eukaryotes, the carbonic anhydrase Nce103 has been shown to be essential for growth in air (~0.04% CO2). Expression of NCE103 is regulated in response to CO2 availability. In Saccharomyces cerevisiae, NCE103 is activated by the transcription factor ScCst6, and in Candida albicans and Candida glabrata, it is activated by its homologues CaRca1 and CgRca1, respectively. To identify the kinase controlling Cst6/Rca1, we screened an S. cerevisiae kinase/phosphatase mutant library for the ability to regulate NCE103 in a CO2-dependent manner. We identified ScSch9 as a potential ScCst6-specific kinase, as the sch9Δ mutant strain showed deregulated NCE103 expression on the RNA and protein levels. Immunoprecipitation revealed the binding capabilities of both proteins, and detection of ScCst6 phosphorylation by ScSch9 in vitro confirmed Sch9 as the Cst6 kinase. We could show that CO2-dependent activation of Sch9, which is part of a kinase cascade, is mediated by lipid/Pkh1/2 signaling but not TORC1. Finally, we tested conservation of the identified regulatory cascade in the pathogenic yeast species C. albicans and C. glabrata. Deletion of SCH9 homologues of both species impaired CO2-dependent regulation of NCE103 expression, which indicates a conservation of the CO2 adaptation mechanism among yeasts. Thus, Sch9 is a Cst6/Rca1 kinase that links CO2 adaptation to lipid signaling via Pkh1/2 in fungi.
url http://mbio.asm.org/cgi/content/full/8/1/e02211-16
work_keys_str_mv AT susannpohlers lipidsignalingviapkh12regulatesfungalco2sensingthroughthekinasesch9
AT ronnymartin lipidsignalingviapkh12regulatesfungalco2sensingthroughthekinasesch9
AT thomaskruger lipidsignalingviapkh12regulatesfungalco2sensingthroughthekinasesch9
AT danielahellwig lipidsignalingviapkh12regulatesfungalco2sensingthroughthekinasesch9
AT frankhanel lipidsignalingviapkh12regulatesfungalco2sensingthroughthekinasesch9
AT olafkniemeyer lipidsignalingviapkh12regulatesfungalco2sensingthroughthekinasesch9
AT hanspetersaluz lipidsignalingviapkh12regulatesfungalco2sensingthroughthekinasesch9
AT patrickvandijck lipidsignalingviapkh12regulatesfungalco2sensingthroughthekinasesch9
AT joachimfernst lipidsignalingviapkh12regulatesfungalco2sensingthroughthekinasesch9
AT axelbrakhage lipidsignalingviapkh12regulatesfungalco2sensingthroughthekinasesch9
AT fritzamuhlschlegel lipidsignalingviapkh12regulatesfungalco2sensingthroughthekinasesch9
AT oliverkurzai lipidsignalingviapkh12regulatesfungalco2sensingthroughthekinasesch9
AT michaellorenz lipidsignalingviapkh12regulatesfungalco2sensingthroughthekinasesch9
_version_ 1721344581731090432