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Updated: Aug 14, 2026

Spatio-Temporal Manipulation of Small GTPase Activity at Subcellular Level and on Timescale of Seconds in Living Cells
Published on: March 9, 2012
Target of rapamycin (TOR): balancing the opposing forces of protein synthesis and degradation
P B Dennis1, S Fumagalli, G Thomas
1Friedrich Miescher Institute, Maulbeerstrasse 66, CH-4058, Basel, Switzerland.
Abstract:
Mitogenic and nutritional signals must be integrated for a cell to grow. The target of rapamycin (TOR) is emerging as an effector for signals which indicate to the cell whether the external environment is conducive for growth. Use of the immunosuppressant rapamycin, a bacterial macrolide, has been instructive in identifying potential signaling components downstream of TOR, leading to the observation that both protein synthesis and turnover are under TOR control. The central issues concerning TOR are the identification of the proliferative and anti-proliferative signals which mediate its function and the mechanisms by which these signals are transduced to downstream molecules.
Insights
Cellular growth requires integrating signals, with the target of rapamycin (TOR) pathway mediating environmental cues. Rapamycin studies reveal TOR controls protein synthesis and turnover, highlighting key research questions on its upstream signals and downstream mechanisms.
Area of Science:
- Cell Biology
- Molecular Signaling
- Biochemistry
Background:
- Cellular growth depends on integrating mitogenic and nutritional signals.
- The target of rapamycin (TOR) pathway is a key mediator of environmental cues for cell growth.
- Rapamycin, an immunosuppressant, has been instrumental in dissecting TOR signaling.
Purpose of the Study:
- To elucidate the role of the target of rapamycin (TOR) pathway in integrating growth signals.
- To identify signaling components downstream of TOR.
- To understand the mechanisms of TOR-mediated control over protein synthesis and turnover.
Main Methods:
- Utilizing the immunosuppressant rapamycin to probe TOR signaling.
- Investigating downstream effectors of TOR.
- Analyzing changes in protein synthesis and turnover.
Main Results:
- Identified downstream signaling components influenced by TOR.
- Demonstrated that both protein synthesis and protein turnover are regulated by TOR.
- Established TOR as a central regulator integrating growth-promoting signals.
Conclusions:
- The TOR pathway is crucial for cellular decision-making regarding growth based on environmental conditions.
- Further research is needed to identify specific proliferative and anti-proliferative signals upstream of TOR.
- Understanding TOR signal transduction is key to comprehending cell growth regulation.
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