Negative regulation of filamentous growth in Candida albicans by Dig1p

Mol Microbiol. 2017 Sep;105(5):810-824. doi: 10.1111/mmi.13738. Epub 2017 Jul 21.

Abstract

Transcriptional regulation involves both positive and negative regulatory elements. The Dig1 negative regulators are part of a fungal-specific module that includes a transcription factor (a Ste12 family member) and a Dig1 family member. In Saccharomyces cerevisiae, the post-genome-duplication Dig1/Dig2 proteins regulate MAP kinase controlled signalling pathways involved in mating and filamentous growth. We have identified the single Dig1 orthologue in the fungal pathogen Candida albicans. Genetic studies and transcriptional profiling experiments show that this single protein is implicated in the regulation of MAP kinase-controlled processes involved in mating, filamentous growth and biofilm formation, and also influences cAMP-regulated processes. This suggests that the multiple cellular roles of the Dig1 protein are ancestral and predate the sub-functionalization apparent in S. cerevisiae after the genome duplication. Intriguingly, even though loss of Dig1 function in C. albicans enhances filamentous growth and biofilm formation, colonization of the murine gastrointestinal tract is reduced in the mutant. The complexity of the processes influenced by Dig1 in C. albicans, and the observation that Dig1 is one of the few regulatory proteins that were retained in the duplicated state after the whole genome duplication event in yeast, emphasizes the important role of these negative regulators in fungal transcriptional control.

MeSH terms

  • Animals
  • Biofilms / growth & development
  • Candida albicans / genetics*
  • Candida albicans / metabolism*
  • Fungal Proteins / metabolism
  • Gene Expression Regulation, Fungal / genetics
  • Mice / microbiology
  • Mitogen-Activated Protein Kinases / metabolism
  • Promoter Regions, Genetic / genetics
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae Proteins / metabolism
  • Signal Transduction
  • Transcription Factors / metabolism
  • Transcription, Genetic / genetics

Substances

  • DIG1 protein, S cerevisiae
  • Fungal Proteins
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors
  • Mitogen-Activated Protein Kinases