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Functional Portrait of Irf1 (Orf19.217), a Regulator of Morphogenesis and Iron Homeostasis in Candida albicans
Lasse van Wijlick1, Sadri Znaidi1,2, Arturo Hernández-Cervantes1
1Institut Pasteur, Université Paris Cité, INRAE USC2019, Unité Biologie et Pathogénicité Fongiques, Paris, France.
Abstract:
The alternate growth of Candida albicans between a unicellular yeast form and a multicellular hyphal form is crucial for its ability to cause disease. Interestingly, both morphological forms support distinct functions during proliferation in the human host. We previously identified ORF19.217 (C2_08890W_A), encoding a zinc-finger transcription factor of the C2H2 family, in a systematic screen of genes whose overexpression contributes to C. albicans' morphological changes. Conditional overexpression of ORF19.217 with the strong tetracycline-inducible promoter (P ) resulted in a hyperfilamentous phenotype. We examined growth of the orf19.217 knockout-mutant in different hypha-inducing conditions and found that the mutant still formed hyphae under standard hypha-inducing conditions. To further investigate the function of Orf19.217 in C. albicans, we combined genome-wide expression (RNA-Seq) and location (ChIP-Seq) analyses. We found that Orf19.217 is involved in regulatory processes comprising hyphal morphogenesis and iron acquisition. Comparative analysis with existing C. albicans hyphal transcriptomes indicates that Orf19.217-mediated filamentation is distinct from a true hyphal program. Further, the orf19.217 knockout-mutant did not show increased sensitivity to iron deprivation, but ORF19.217 overexpression was able to rescue the growth of a hap5-mutant, defective in a subunit of the CCAAT-complex, which is essential for iron acquisition. This suggested that Orf19.217 is involved in regulation of iron acquisition genes during iron deprivation and acts in a parallel pathway to the established CCAAT-complex. Interestingly, the orf19.217-mutant turned out to be defective in its ability to form filaments under iron-deficiency. Taken together our findings propose that the transcription factor Orf19.217 stimulates expression of the hyphal regulators EFG1 and BRG1 to promote filamentous growth under iron deprivation conditions, allowing the fungus to escape these iron-depleted conditions. The transcription factor therefore appears to be particularly important for adaptation of C. albicans to diverse environmental conditions in the human host. In regard to the newly identified functions, we have given the regulator the name Irf1, Iron-dependent Regulator of Filamentation.
Insights
Candida albicans uses the transcription factor Orf19.217 (Irf1) to form hyphae, crucial for disease. Irf1 regulates iron acquisition and hyphal growth, particularly under iron-deprived conditions, aiding fungal adaptation.
Area of Science:
- Mycology
- Molecular Biology
- Medical Microbiology
Background:
- Candida albicans exhibits dimorphism, switching between yeast and hyphal forms, which is vital for pathogenesis.
- The transcription factor Orf19.217 was identified for its role in regulating C. albicans morphology.
Purpose of the Study:
- To investigate the function of Orf19.217 in C. albicans morphology and iron acquisition.
- To elucidate the regulatory role of Orf19.217 in fungal adaptation to host environments.
Main Methods:
- Conditional overexpression and knockout mutant analysis of ORF19.217.
- Genome-wide expression (RNA-Seq) and location (ChIP-Seq) analyses.
- Comparative analysis with existing C. albicans hyphal transcriptomes.
Main Results:
- Orf19.217 (named Irf1) is involved in hyphal morphogenesis and iron acquisition.
- Irf1-mediated filamentation is distinct from the canonical hyphal program.
- The orf19.217 mutant is defective in hyphal formation under iron deficiency, but Irf1 overexpression rescues a hap5-mutant defective in iron acquisition.
Conclusions:
- The transcription factor Irf1 promotes filamentous growth under iron deprivation by stimulating hyphal regulators EFG1 and BRG1.
- Irf1 is essential for C. albicans adaptation to iron-limited conditions within the human host.
- Irf1 acts in a parallel pathway to the CCAAT-complex for iron acquisition regulation.
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