TORC1-Dependent Phosphorylation Targets in Fission Yeast

Biomolecules. 2017 Jul 3;7(3):50. doi: 10.3390/biom7030050.

Abstract

Target of rapamycin (TOR) kinase controls cell metabolism and growth in response to environmental cues such as nutrients, growth factors, and stress. TOR kinase is widely conserved across eukaryotes. As in other organisms, the fission yeast Schizosaccharomyces pombe has two types of TOR complex, namely TOR complex 1 (TORC1) and TORC2. It is interesting that the two TOR complexes in S. pombe have opposite roles in sexual differentiation, which is induced by nutrient starvation. TORC1, which contains Tor2 as a catalytic subunit, promotes vegetative growth and represses sexual differentiation in nutrient-rich conditions, while TORC2 is required for the initiation of sexual differentiation. Multiple targets of TORC1 have been identified. Some of these, such as S6 kinase and an autophagy regulator Atg13, are known targets in other organisms. In addition, there is a novel group of TORC1 targets involved in the regulation of sexual differentiation. Here, we review recent findings on phosphorylation targets of TORC1 in S. pombe. Furthermore, we briefly report a novel S. pombe target of TORC1.

Keywords: TOR complex 1; fission yeast; sexual differentiation.

Publication types

  • Review

MeSH terms

  • Autophagy-Related Proteins / metabolism
  • Gene Expression Regulation, Developmental
  • Gene Expression Regulation, Fungal
  • Mechanistic Target of Rapamycin Complex 1 / metabolism*
  • Phosphorylation
  • Ribosomal Protein S6 Kinases / metabolism
  • Schizosaccharomyces / growth & development*
  • Schizosaccharomyces / metabolism
  • Schizosaccharomyces pombe Proteins / metabolism

Substances

  • Atg13 protein, S pombe
  • Autophagy-Related Proteins
  • Schizosaccharomyces pombe Proteins
  • Mechanistic Target of Rapamycin Complex 1
  • Ribosomal Protein S6 Kinases