The S. pombe SAGA complex controls the switch from proliferation to sexual differentiation through the opposing roles of its subunits Gcn5 and Spt8

Dominique Helmlinger (1) , S. Marguerat (2) , J. Villén (3) , S. Gygi (3) , J. Bahler (2) , F. Winston (4)

1 CRBM - Centre de recherche en Biologie Cellulaire
2 The Wellcome Trust Sanger Institute [Cambridge]
3 Department of cell biology
4 Department of Genetics [Boston]

The SAGA complex is a conserved multifunctional coactivator known to play broad roles in eukaryotic transcription. To gain new insights into its functions, we performed biochemical and genetic analyses of SAGA in the fission yeast, Schizosaccharomyces pombe. Purification of the S. pombe SAGA complex showed that its subunit composition is identical to that of Saccharomyces cerevisiae. Analysis of S. pombe SAGA mutants revealed that SAGA has two opposing roles regulating sexual differentiation. First, in nutrient-rich conditions, the SAGA histone acetyltransferase Gcn5 represses ste11+, which encodes the master regulator of the mating pathway. In contrast, the SAGA subunit Spt8 is required for the induction of ste11+ upon nutrient starvation. Chromatin immunoprecipitation experiments suggest that these regulatory effects are direct, as SAGA is physically associated with the ste11+ promoter independent of nutrient levels. Genetic tests suggest that nutrient levels do cause a switch in SAGA function, as spt8Δ suppresses gcn5Δ with respect to ste11+ derepression in rich medium, whereas the opposite relationship, gcn5Δ suppression of spt8Δ, occurs during starvation. Thus, SAGA plays distinct roles in the control of the switch from proliferation to differentiation in S. pombe through the dynamic and opposing activities of Gcn5 and Spt8.

Mots clés: S. pombe; transcription; differentiation; SAGA; Gcn5; Ste11

Domaines: Génomique, Transcriptomique et Protéomique [q-bio.GN]

Dominique Helmlinger, S. Marguerat, J. Villén, S. Gygi, J. Bahler, et al.. The S. pombe SAGA complex controls the switch from proliferation to sexual differentiation through the opposing roles of its subunits Gcn5 and Spt8. Genes and Development, 2008, 22 (22), pp.3184-3195. ⟨10.1101/gad.1719908⟩. ⟨hal-02371840⟩