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dc.contributor.authorMoran, Gary P
dc.date.accessioned2013-05-21T12:02:11Z
dc.date.available2013-05-21T12:02:11Z
dc.date.issued2012-12
dc.identifier.citationTranscript profiling reveals rewiring of iron assimilation gene expression in Candida albicans and C. dubliniensis. 2012, 12 (8):918-23 FEMS Yeast Res.en_GB
dc.identifier.issn1567-1364
dc.identifier.pmid22888912
dc.identifier.doi10.1111/j.1567-1364.2012.00841.x
dc.identifier.urihttp://hdl.handle.net/10147/292522
dc.description.abstractHyphal growth is repressed in Candida albicans and Candida dubliniensis by the transcription factor Nrg1. Transcript profiling of a C. dubliniensis NRG1 mutant identified a common group of 28 NRG1-repressed genes in both species, including the hypha-specific genes HWP1, ECE1 and the regulator of cell elongation UME6. Unexpectedly, C. dubliniensis NRG1 was required for wild-type levels of expression of 10 genes required for iron uptake including seven ferric reductases, SIT1, FTR1 and RBT5. However, at alkaline pH and during filamentous growth in 10% serum, most of these genes were highly induced in C. dubliniensis. Conversely, RBT5, PGA10, FRE10 and FRP1 did not exhibit induction during hyphal growth when NRG1 is downregulated, indicating that in C. dubliniensis NRG1 is also required for optimal expression of these genes in alkaline environments. In iron-depleted medium at pH 4.5, reduced growth of the NRG1 mutant relative to wild type was observed; however, growth was restored to wild-type levels or greater at pH 6.5, indicating that alkaline induction of iron assimilation gene expression could rescue this phenotype. These data indicate that transcriptional control of iron assimilation and pseudohypha formation has been separated in C. albicans, perhaps promoting growth in a wider range of niches.
dc.language.isoenen
dc.publisherFEMS yeast researchen_GB
dc.rightsArchived with thanks to FEMS yeast researchen_GB
dc.subject.meshCandida
dc.subject.meshCandida albicans
dc.subject.meshFungal Proteins
dc.subject.meshGene Expression Profiling
dc.subject.meshGene Expression Regulation, Fungal
dc.subject.meshHyphae
dc.subject.meshIron
dc.subject.meshRepressor Proteins
dc.subject.meshTranscription Factors
dc.subject.meshTranscriptome
dc.titleTranscript profiling reveals rewiring of iron assimilation gene expression in Candida albicans and C. dubliniensis.en_GB
dc.typeArticleen
dc.contributor.departmentDivision of Oral Biosciences, Dublin Dental School and Hospital, Trinity College Dublin, University of Dublin, Ireland. gpmoran@dental.tcd.ieen_GB
dc.identifier.journalFEMS yeast researchen_GB
dc.description.provinceLeinsteren
html.description.abstractHyphal growth is repressed in Candida albicans and Candida dubliniensis by the transcription factor Nrg1. Transcript profiling of a C. dubliniensis NRG1 mutant identified a common group of 28 NRG1-repressed genes in both species, including the hypha-specific genes HWP1, ECE1 and the regulator of cell elongation UME6. Unexpectedly, C. dubliniensis NRG1 was required for wild-type levels of expression of 10 genes required for iron uptake including seven ferric reductases, SIT1, FTR1 and RBT5. However, at alkaline pH and during filamentous growth in 10% serum, most of these genes were highly induced in C. dubliniensis. Conversely, RBT5, PGA10, FRE10 and FRP1 did not exhibit induction during hyphal growth when NRG1 is downregulated, indicating that in C. dubliniensis NRG1 is also required for optimal expression of these genes in alkaline environments. In iron-depleted medium at pH 4.5, reduced growth of the NRG1 mutant relative to wild type was observed; however, growth was restored to wild-type levels or greater at pH 6.5, indicating that alkaline induction of iron assimilation gene expression could rescue this phenotype. These data indicate that transcriptional control of iron assimilation and pseudohypha formation has been separated in C. albicans, perhaps promoting growth in a wider range of niches.


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