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Updated: Jul 2, 2026

Microscopy of Fission Yeast Sexual Lifecycle
Published on: March 9, 2016
TOR signaling in fission yeast
Yoko Otsubo1, Masayuki Yamamato
1Department of Biophysics and Biochemistry, Graduate School of Science, University of Tokyo, Hongo, Tokyo, Japan.
Abstract:
Fission yeast has two TOR kinases, Tor1 and Tor2. Recent studies have indicated that this microbe has a TSC/Rheb/TOR pathway like higher eukaryotes. Two TOR complexes, namely TORC1 and TORC2, have been identified in this yeast, as in budding yeast and mammals. Fission yeast TORC1, which contains Tor2, and TORC2, which contains Tor1, apparently have opposite functions with regard to the promotion of G1 arrest and sexual development. Rapamycin does not inhibit growth of wild-type fission yeast cells, unlike other eukaryotic cells, but precise analyses have revealed that rapamycin affects certain cellular functions involving TOR in this yeast. It appears that fission yeast has a potential to be an ideal model system to investigate the TOR signaling pathways.
Insights
Fission yeast possesses two TOR kinases, Tor1 and Tor2, with distinct roles in cell cycle and development. This microbe offers a model for studying TOR signaling pathways, even though rapamycin has limited effects on its growth.
Area of Science:
- Molecular Biology
- Cell Biology
- Yeast Genetics
Background:
- Fission yeast, like higher eukaryotes, exhibits a TSC/Rheb/TOR signaling pathway.
- Two distinct TOR complexes, TORC1 and TORC2, have been identified in fission yeast.
- TORC1 contains Tor2, while TORC2 contains Tor1, suggesting specialized functions.
Purpose of the Study:
- To investigate the opposing functions of fission yeast TORC1 and TORC2.
- To explore the role of TOR signaling in G1 arrest and sexual development.
- To understand the effects of rapamycin on fission yeast TOR pathways.
Main Methods:
- Analysis of TORC1 and TORC2 composition and function.
- Investigation of G1 arrest and sexual development pathways.
- Detailed examination of rapamycin's effects on cellular functions.
Main Results:
- Fission yeast TORC1 (containing Tor2) and TORC2 (containing Tor1) display opposing roles in promoting G1 arrest and sexual development.
- Rapamycin does not inhibit wild-type fission yeast growth but impacts specific TOR-mediated cellular functions.
- The identified TOR pathway components and their functions are conserved across eukaryotes.
Conclusions:
- Fission yeast TORC1 and TORC2 have divergent functions in regulating cell cycle and development.
- Despite resistance to growth inhibition, rapamycin reveals specific roles for TOR signaling in fission yeast.
- Fission yeast serves as a valuable model organism for dissecting conserved TOR signaling pathways.
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