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| Status |
Public on Jun 30, 2017 |
| Title |
Genome-wide expression profiling of Candida albicans transcription factor Skn7p |
| Organism |
Candida albicans |
| Experiment type |
Expression profiling by array
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| Summary |
Skn7 is a conserved fungal heat shock factor-type transcriptional regulator. It participates in maintaining cell wall integrity and regulates the osmotic/oxidative stress response (OSR) in S. cerevisiae, where it is part of a two-component signal transduction system. Here, we comprehensively address the function of Skn7 in the human fungal pathogen Candida albicans. We provide evidence reinforcing functional divergence, with loss of the cell wall/osmotic stress-protective roles and acquisition of the ability to regulate morphogenesis on solid medium. Mapping of the Skn7 transcriptional circuitry, through combination of genome-wide expression and location technologies, pointed to a dual regulatory role encompassing OSR and filamentous growth. Genetic interaction analyses revealed close functional interactions between Skn7 and master regulators of morphogenesis, including Efg1, Cph1 and Ume6. Intracellular biochemical assays revealed that Skn7 is crucial for limiting the accumulation of reactive oxygen species (ROS) during filamentous growth on solid medium. Interestingly, functional domain mapping using site-directed mutagenesis allowed decoupling of Skn7 function in morphogenesis from protection against intracellular ROS. Our work identifies Skn7 as an integral part of the transcriptional circuitry controlling C. albicans filamentous growth and illuminates how C. albicans relies on an evolutionarily-conserved regulator to protect itself from intracellular ROS during morphological development.
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| Overall design |
Two-condition experiments: Reverse-transcribed RNA from Anhydrotetracycline (ATc)-untreated (Cy3-labeled) and ATc-treated (Cy5-labeled) C. albicans strains carrying i) a SKN7 allele placed under the control of the tetracycline derivative-inducible promoter (Samples 1-8) or ii) the empty vector control (samples 9-16) and grown during 0, 2 and 4h in liquid rich (Yeast Peptone Dextrose) medium at 30ºC. Samples 1-2 and 9-10: time point 0 h (2 replicates), samples 3-5 and 11-13: time point 2 h (3 replicates) and samples 6-8 and 14-16: time point 4h (3 replicates).
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| Contributor(s) |
Znaidi S |
| Citation(s) |
28752552 |
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| Submission date |
Aug 07, 2016 |
| Last update date |
Sep 30, 2017 |
| Contact name |
Sadri ZNAIDI |
| E-mail(s) |
sadri.znaidi@gmail.com
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| Organization name |
Institut Pasteur
|
| Department |
Mycology Department
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| Lab |
Fungal Biology and Pathogenicity
|
| Street address |
25 rue du Docteur Roux
|
| City |
Paris |
| ZIP/Postal code |
75015 |
| Country |
France |
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| Platforms (1) |
| GPL19932 |
Agilent G2534A oligonucleotide-microarray (AMADID:026869) (Probe Name version) |
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| Samples (16)
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| Relations |
| BioProject |
PRJNA338060 |
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