DOI | Resolve DOI: https://doi.org/10.1371/journal.pone.0043956 |
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Author | Search for: Sellam, A.; Search for: Tebbji, F.1; Search for: Whiteway, M.1; Search for: Nantel, A.1 |
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Affiliation | - National Research Council of Canada. NRC Biotechnology Research Institute
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Format | Text, Article |
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Subject | transcription factor; transcription factor Cwt1p; unclassified drug; Candida albicans; fungal genome; fungus mutant; gene activation; gene expression; gene expression profiling; gene location; gene regulatory network; gene repression; genetic analysis; host cell; nitrosative stress; phagocyte; regulon; transcription regulation; Candida albicans; Fungal Proteins; Gene Expression Profiling; Gene Expression Regulation, Fungal; Genomics; Oxygenases; Promoter Regions, Genetic; Reactive Nitrogen Species; Stress, Physiological; Transcription Factors; Transcription, Genetic; Candida albicans; Fungi; Mammalia |
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Abstract | The ability of Candida albicans to survive in the presence of nitrosative stress during the initial contact with the host immune system is crucial for its ability to colonize mammalian hosts. Thus, this fungus must activate robust mechanisms to neutralize and repair nitrosative-induced damage. Until now, very little was known regarding the regulatory circuits associated with reactive nitrogen species detoxification in fungi. To gain insight into the transcriptional regulatory networks controlling nitrosative stress response (NRS) in C. albicans a compilation of transcriptional regulator-defective mutants were screened. This led to the identification of Cwt1p as a negative regulator of NSR. By combining genome-wide location and expression analyses, we have characterized the Cwt1p regulon and demonstrated that Cwt1p is directly required for proper repression of the flavohemoglobin Yhb1p, a key NO-detoxification enzyme. Furthermore, Cwt1p operates both by activating and repressing genes of specific functions solicited upon NSR. Additionally, we used Gene Set Enrichment Analysis to reinvestigate the C. albicans NSR-transcriptome and demonstrate a significant similarity with the transcriptional profiles of C. albicans interacting with phagocytic host-cells. In summary, we have characterized a novel negative regulator of NSR and bring new insights into the transcriptional regulatory network governing fungal NSR. © 2012 Sellam et al. |
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Publication date | 2012 |
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In | |
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Language | English |
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Peer reviewed | Yes |
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NPARC number | 21269180 |
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Export citation | Export as RIS |
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Report a correction | Report a correction (opens in a new tab) |
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Record identifier | 34be012a-2267-48bd-9143-3d9a9efd673f |
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Record created | 2013-12-12 |
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Record modified | 2021-09-17 |
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