Structural requirements for sterol regulatory element-binding protein (SREBP) cleavage in fission yeast

J Biol Chem. 2013 Jul 12;288(28):20351-60. doi: 10.1074/jbc.M113.482224. Epub 2013 May 31.


Sterol regulatory element-binding proteins (SREBPs) are central regulators of cellular lipid synthesis and homeostasis. Mammalian SREBPs are proteolytically activated and liberated from the membrane by Golgi Site-1 and Site-2 proteases. Fission yeast SREBPs, Sre1 and Sre2, employ a different mechanism that genetically requires the Golgi Dsc E3 ligase complex for cleavage activation. Here, we established Sre2 as a model to define structural requirements for SREBP cleavage. We showed that Sre2 cleavage does not require the N-terminal basic helix-loop-helix zipper transcription factor domain, thus separating cleavage of Sre2 from its transcription factor function. From a mutagenesis screen of 94 C-terminal residues of Sre2, we isolated 15 residues required for cleavage and further identified a glycine-leucine sequence required for Sre2 cleavage. Importantly, the glycine-leucine sequence is located at a conserved distance before the first transmembrane segment of both Sre1 and Sre2 and cleavage occurs in between this sequence and the membrane. Bioinformatic analysis revealed a broad conservation of this novel glycine-leucine motif in SREBP homologs of ascomycete fungi, including the opportunistic human pathogen Aspergillus fumigatus where SREBP is required for virulence. Consistent with this, the sequence was also required for cleavage of the oxygen-responsive transcription factor Sre1 and adaptation to hypoxia, demonstrating functional conservation of this cleavage recognition motif. These cleavage mutants will aid identification of the fungal SREBP protease and facilitate functional dissection of the Dsc E3 ligase required for SREBP activation and fungal pathogenesis.

Keywords: Fungal Pathogenesis; Glycine-Leucine Motif; Hypoxia; Lipids; Protein Motifs; Proteolytic Cleavage; SREBP; Sterol; Transcription Factors.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / metabolism
  • Amino Acid Motifs / genetics
  • Amino Acid Sequence
  • Anaerobiosis
  • Blotting, Western
  • Cell Cycle Proteins / metabolism
  • Glycine / genetics
  • Glycine / metabolism
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Leucine / genetics
  • Leucine / metabolism
  • Microscopy, Fluorescence
  • Models, Genetic
  • Mutation*
  • Oxygen / metabolism
  • Oxygen / pharmacology
  • Proteolysis / drug effects
  • Schizosaccharomyces / drug effects
  • Schizosaccharomyces / genetics*
  • Schizosaccharomyces / metabolism
  • Schizosaccharomyces pombe Proteins / genetics*
  • Schizosaccharomyces pombe Proteins / metabolism
  • Sterol Regulatory Element Binding Protein 2 / genetics
  • Sterol Regulatory Element Binding Protein 2 / metabolism
  • Sterol Regulatory Element Binding Proteins / genetics*
  • Sterol Regulatory Element Binding Proteins / metabolism
  • Ubiquitin-Conjugating Enzymes / metabolism
  • Ubiquitin-Protein Ligases / metabolism
  • Valosin Containing Protein


  • Cell Cycle Proteins
  • Schizosaccharomyces pombe Proteins
  • Sre1 protein, S pombe
  • Sterol Regulatory Element Binding Protein 2
  • Sterol Regulatory Element Binding Proteins
  • Green Fluorescent Proteins
  • Ubc4 protein, S pombe
  • Ubiquitin-Conjugating Enzymes
  • Ubiquitin-Protein Ligases
  • Adenosine Triphosphatases
  • Valosin Containing Protein
  • Leucine
  • Oxygen
  • Glycine