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Updated: Feb 27, 2026

Examination of Mitotic and Meiotic Fission Yeast Nuclear Dynamics by Fluorescence Live-cell Microscopy
Published on: June 24, 2019
TORC1-Dependent Phosphorylation Targets in Fission Yeast
Yoko Otsubo1, Akio Nakashima2, Masayuki Yamamoto3,4
1Laboratory of Cell Responses, National Institute for Basic Biology, Nishigonaka 38, Myodaiji, Okazaki, Aichi 444-8585, Japan. otsubo@nibb.ac.jp.
Target of rapamycin (TOR) kinase regulates cell growth and metabolism. In fission yeast, TOR complex 1 (TORC1) and TOR complex 2 (TORC2) have opposing roles in sexual differentiation, with TORC1 repressing it and TORC2 promoting it.
Area of Science:
- Molecular Biology
- Cell Biology
- Biochemistry
Background:
- Target of rapamycin (TOR) kinase is a crucial regulator of cell metabolism and growth, conserved across eukaryotes.
- Fission yeast, *Schizosaccharomyces pombe*, possesses two TOR complexes: TORC1 and TORC2, which play significant roles in cellular processes.
- TORC1, containing Tor2, promotes growth and represses sexual differentiation under nutrient-rich conditions.
Purpose of the Study:
- To review recent findings on the phosphorylation targets of TORC1 in *S. pombe*.
- To elucidate the opposing roles of TORC1 and TORC2 in sexual differentiation.
- To report a novel TORC1 target in *S. pombe*.
Main Methods:
- Literature review of TORC1 phosphorylation targets.
- Analysis of TORC1 and TORC2 functions in sexual differentiation.
- Identification and characterization of novel TORC1 targets.
Main Results:
- TORC1 and TORC2 exhibit opposing functions in *S. pombe* sexual differentiation, which is triggered by nutrient starvation.
- Known TORC1 targets like S6 kinase and Atg13 are conserved in *S. pombe*.
- A novel group of TORC1 targets involved in regulating sexual differentiation has been identified.
Conclusions:
- TORC1 and TORC2 differentially regulate sexual differentiation in response to nutrient availability.
- Understanding TORC1 targets provides insights into cell growth, metabolism, and differentiation pathways.
- Further research on novel TORC1 targets will enhance our knowledge of *S. pombe* biology.
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