Literature DB >> 11532939

NRG1, a repressor of filamentous growth in C.albicans, is down-regulated during filament induction.

B R Braun1, D Kadosh, A D Johnson.   

Abstract

In response to a variety of external signals, the fungal pathogen Candida albicans undergoes a transition between ellipsoidal single cells (blastospores) and filaments composed of elongated cells attached end-to-end. Here we identify a DNA-binding protein, Nrg1, that represses filamentous growth in Candida probably by acting through the co-repressor Tup1. nrg1 mutant cells are predominantly filamentous under non-filament-inducing conditions and their colony morphology resembles that of tup1 mutants. We also identify two filament-specific genes, ECE1 and HWP1, whose transcription is repressed by Nrg1 under non-inducing conditions. These genes constitute a subset of those under Tup1 control, providing further evidence that Nrg1 acts by recruiting Tup1 to target genes. We show that growth in serum at 37 degrees C, a potent inducer of filamentous growth, causes a reduction of NRG1 mRNA, suggesting that filamentous growth is induced by the down-regulation of NRG1. Consistent with this idea, expression of NRG1 from a non-regulated promoter partially blocks the induction of filamentous growth.

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Year:  2001        PMID: 11532939      PMCID: PMC125265          DOI: 10.1093/emboj/20.17.4753

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  48 in total

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6.  Identification and characterization of TUP1-regulated genes in Candida albicans.

Authors:  B R Braun; W S Head; M X Wang; A D Johnson
Journal:  Genetics       Date:  2000-09       Impact factor: 4.562

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Review 10.  Pathogenesis of Candida infections.

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Journal:  J Am Acad Dermatol       Date:  1994-09       Impact factor: 11.527

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  153 in total

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Journal:  Eukaryot Cell       Date:  2005-03

9.  Expression of UME6, a key regulator of Candida albicans hyphal development, enhances biofilm formation via Hgc1- and Sun41-dependent mechanisms.

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10.  Engineered control of cell morphology in vivo reveals distinct roles for yeast and filamentous forms of Candida albicans during infection.

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