Interplay of the fungal sumoylation network for control of multicellular development

Mol Microbiol. 2013 Dec;90(5):1125-45. doi: 10.1111/mmi.12421. Epub 2013 Nov 6.

Abstract

The role of the complex network of the ubiquitin-like modifier SumO in fungal development was analysed. SumO is not only required for sexual development but also for accurate induction and light stimulation of asexual development. The Aspergillus nidulans COMPASS complex including its subunits CclA and the methyltransferase SetA connects the SumO network to histone modification. SetA is required for correct positioning of aerial hyphae for conidiophore and asexual spore formation. Multicellular fungal development requires sumoylation and desumoylation. This includes the SumO processing enzyme UlpB, the E1 SumO activating enzyme AosA/UbaB, the E2 conjugation enzyme UbcN and UlpA as major SumO isopeptidase. Genetic suppression analysis suggests a connection between the genes for the Nedd8 isopeptidase DenA and the SumO isopeptidase UlpA and therefore a developmental interplay between neddylation and sumoylation in fungi. Biochemical evidence suggests an additional connection of the fungal SumO network with ubiquitination. Members of the cellular SumO network include histone modifiers, components of the transcription, RNA maturation and stress response machinery, or metabolic enzymes. Our data suggest that the SumO network controls specific temporal and spatial steps in fungal differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aspergillus nidulans / genetics
  • Aspergillus nidulans / growth & development*
  • Aspergillus nidulans / metabolism*
  • Carrier Proteins
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism*
  • Genes, Fungal*
  • Hyphae / metabolism
  • Methyltransferases / genetics
  • Methyltransferases / metabolism
  • Peptide Hydrolases / metabolism
  • Protein Processing, Post-Translational
  • Small Ubiquitin-Related Modifier Proteins / genetics
  • Small Ubiquitin-Related Modifier Proteins / metabolism*
  • Sumoylation
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Ubiquitin-Conjugating Enzymes / metabolism
  • Ubiquitins / metabolism

Substances

  • Carrier Proteins
  • Fungal Proteins
  • SIMC1 protein, human
  • Small Ubiquitin-Related Modifier Proteins
  • Transcription Factors
  • Ubiquitins
  • Methyltransferases
  • Ubiquitin-Conjugating Enzymes
  • Peptide Hydrolases