The APSES protein Sok2 is a positive regulator of sporulation in Ashbya gossypii

Mol Microbiol. 2017 Dec;106(6):949-960. doi: 10.1111/mmi.13859. Epub 2017 Oct 23.

Abstract

Ashbya gossypii is a homothallic, flavinogenic, filamentous ascomycete that starts overproduction of riboflavin and fragments its mycelium quantitatively into spore producing sporangia at the end of a growth phase. Mating is not required for sporulation and the standard homothallic laboratory strain is a MATa strain. Here we show that ectopic expression of Saccharomyces cerevisiae MATα2 in A. gossypii completely suppresses sporulation, inhibits riboflavin overproduction and downregulates among others AgSOK2. AgSok2 belongs to a fungal-specific group of (APSES) transcription factors. Deletion of AgSOK2 strongly reduces riboflavin production and blocks sporulation. The initiator of meiosis, AgIME1, is a transcription factor essential for sporulation. We characterized the AgIME1 promoter region required for complementation of the Agime1 mutant. Reporter assays with AgIME1 promoter fragments fused to lacZ showed that AgSok2 does not control AgIME1 transcription. However, global transcriptome analysis identified two other essential regulators of sporulation, AgIME2 and AgNDT80, as potential targets of AgSok2. Our data suggest that sporulation and riboflavin production in A. gossypii are under mating type locus and nutritional control. Sok2, a target of the cAMP/protein kinase A pathway, serves as a central positive regulator to promote sporulation. This contrasts Saccharomyces cerevisiae where Sok2 is a repressor of IME1 transcription.

MeSH terms

  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Eremothecium / genetics
  • Eremothecium / physiology*
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism*
  • Gene Deletion
  • Gene Expression Profiling
  • Gene Expression Regulation, Fungal
  • Meiosis
  • Promoter Regions, Genetic
  • Protein Precursors / genetics
  • Protein Precursors / metabolism*
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*
  • Riboflavin / metabolism
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Spores, Fungal / genetics
  • Spores, Fungal / physiology*
  • Transcription Factors / metabolism

Substances

  • Fungal Proteins
  • MF(ALPHA)1 protein, S cerevisiae
  • Protein Precursors
  • Repressor Proteins
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors
  • Cyclic AMP-Dependent Protein Kinases
  • Riboflavin