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Published on: October 23, 2018
Regulation and function of ribosomal protein S6 kinase (S6K) within mTOR signalling networks
Brian Magnuson1, Bilgen Ekim, Diane C Fingar
1Department of Cell and Developmental Biology, University of Michigan Medical School, 109 Zina Pitcher Place, Ann Arbor, MI 48109-2200, USA.
Abstract:
The ribosomal protein S6K (S6 kinase) represents an extensively studied effector of the TORC1 [TOR (target of rapamycin) complex 1], which possesses important yet incompletely defined roles in cellular and organismal physiology. TORC1 functions as an environmental sensor by integrating signals derived from diverse environmental cues to promote anabolic and inhibit catabolic cellular functions. mTORC1 (mammalian TORC1) phosphorylates and activates S6K1 and S6K2, whose first identified substrate was rpS6 (ribosomal protein S6), a component of the 40S ribosome. Studies over the past decade have uncovered a number of additional S6K1 substrates, revealing multiple levels at which the mTORC1-S6K1 axis regulates cell physiology. The results thus far indicate that the mTORC1-S6K1 axis controls fundamental cellular processes, including transcription, translation, protein and lipid synthesis, cell growth/size and cell metabolism. In the present review we summarize the regulation of S6Ks, their cellular substrates and functions, and their integration within rapidly expanding mTOR (mammalian TOR) signalling networks. Although our understanding of the role of mTORC1-S6K1 signalling in physiology remains in its infancy, evidence indicates that this signalling axis controls, at least in part, glucose homoeostasis, insulin sensitivity, adipocyte metabolism, body mass and energy balance, tissue and organ size, learning, memory and aging. As dysregulation of this signalling axis contributes to diverse disease states, improved understanding of S6K regulation and function within mTOR signalling networks may enable the development of novel therapeutics.
Insights
The mammalian target of rapamycin complex 1 (mTORC1)-S6 kinase (S6K) pathway regulates fundamental cellular processes like growth and metabolism. This review details S6K
Area of Science:
- Cellular and Molecular Biology
- Physiology
- Biochemistry
Background:
- The target of rapamycin complex 1 (TORC1) pathway is a crucial environmental sensor regulating cellular anabolism and catabolism.
- Ribosomal protein S6 kinase (S6K) is a key effector of TORC1, with roles in cellular physiology that are still being defined.
- mTORC1 phosphorylates and activates S6K1 and S6K2, initially identified through their substrate ribosomal protein S6 (rpS6).
Purpose of the Study:
- To review the regulation, substrates, and functions of S6 kinases (S6Ks).
- To explore the integration of S6Ks within mammalian target of rapamycin (mTOR) signaling networks.
- To highlight the physiological and pathophysiological roles of the mTORC1-S6K1 signaling axis.
Main Methods:
- Literature review of studies on S6K regulation, substrates, and functions.
- Analysis of the integration of S6K signaling within broader mTOR networks.
- Synthesis of evidence linking mTORC1-S6K1 signaling to various physiological processes and diseases.
Main Results:
- The mTORC1-S6K1 axis regulates transcription, translation, protein and lipid synthesis, cell growth, and metabolism.
- Recent research has identified numerous additional S6K1 substrates beyond rpS6.
- Evidence suggests mTORC1-S6K1 signaling influences glucose homeostasis, insulin sensitivity, adiposity, energy balance, organ size, learning, memory, and aging.
Conclusions:
- The mTORC1-S6K1 pathway controls fundamental cellular processes and organismal physiology.
- Dysregulation of this pathway is implicated in various diseases.
- Further understanding of S6K regulation and function within mTOR networks may lead to new therapeutic strategies.
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