Abf1 and other general regulatory factors control ribosome biogenesis gene expression in budding yeast

Nucleic Acids Res. 2017 May 5;45(8):4493-4506. doi: 10.1093/nar/gkx058.

Abstract

Ribosome biogenesis in Saccharomyces cerevisiae involves a regulon of >200 genes (Ribi genes) coordinately regulated in response to nutrient availability and cellular growth rate. Two cis-acting elements called PAC and RRPE are known to mediate Ribi gene repression in response to nutritional downshift. Here, we show that most Ribi gene promoters also contain binding sites for one or more General Regulatory Factors (GRFs), most frequently Abf1 and Reb1, and that these factors are enriched in vivo at Ribi promoters. Abf1/Reb1/Tbf1 promoter association was required for full Ribi gene expression in rich medium and for its modulation in response to glucose starvation, characterized by a rapid drop followed by slow recovery. Such a response did not entail changes in Abf1 occupancy, but it was paralleled by a quick increase, followed by slow decrease, in Rpd3L histone deacetylase occupancy. Remarkably, Abf1 site disruption also abolished Rpd3L complex recruitment in response to starvation. Extensive mutational analysis of the DBP7 promoter revealed a complex interplay of Tbf1 sites, PAC and RRPE in the transcriptional regulation of this Ribi gene. Our observations point to GRFs as new multifaceted players in Ribi gene regulation both during exponential growth and under repressive conditions.

MeSH terms

  • Culture Media / chemistry
  • Culture Media / pharmacology
  • DEAD-box RNA Helicases / genetics
  • DEAD-box RNA Helicases / metabolism
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • Gene Expression Regulation, Fungal*
  • Glucose / deficiency
  • Glucose / pharmacology
  • Histone Deacetylase 1 / genetics
  • Histone Deacetylase 1 / metabolism
  • Organelle Biogenesis
  • Promoter Regions, Genetic
  • Regulon
  • Ribosomes / genetics*
  • Ribosomes / metabolism
  • Saccharomyces cerevisiae / drug effects
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae / growth & development
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae Proteins / genetics*
  • Saccharomyces cerevisiae Proteins / metabolism
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Transcription, Genetic

Substances

  • ABF1 protein, S cerevisiae
  • Culture Media
  • DNA-Binding Proteins
  • REB1 protein, S cerevisiae
  • Saccharomyces cerevisiae Proteins
  • TBF1 protein, S cerevisiae
  • Transcription Factors
  • Histone Deacetylase 1
  • DBP7 protein, S cerevisiae
  • DEAD-box RNA Helicases
  • Glucose