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Published on: October 23, 2018
Amino acid regulation of TOR complex 1
Joseph Avruch1, Xiaomeng Long, Sara Ortiz-Vega
1Department of Molecular Biology and Diabetes Research Unit, Medical Service, Massachusetts General Hospital, and Department of Medicine, Harvard Medical School, Simches Research Center, Boston, MA 02114, USA. avruch@molbio.mgh.harvard.edu
Abstract:
TOR complex 1 (TORC1), an oligomer of the mTOR (mammalian target of rapamycin) protein kinase, its substrate binding subunit raptor, and the polypeptide Lst8/GbetaL, controls cell growth in all eukaryotes in response to nutrient availability and in metazoans to insulin and growth factors, energy status, and stress conditions. This review focuses on the biochemical mechanisms that regulate mTORC1 kinase activity, with special emphasis on mTORC1 regulation by amino acids. The dominant positive regulator of mTORC1 is the GTP-charged form of the ras-like GTPase Rheb. Insulin, growth factors, and a variety of cellular stressors regulate mTORC1 by controlling Rheb GTP charging through modulating the activity of the tuberous sclerosis complex, the Rheb GTPase activating protein. In contrast, amino acids, especially leucine, regulate mTORC1 by controlling the ability of Rheb-GTP to activate mTORC1. Rheb binds directly to mTOR, an interaction that appears to be essential for mTORC1 activation. In addition, Rheb-GTP stimulates phospholipase D1 to generate phosphatidic acid, a positive effector of mTORC1 activation, and binds to the mTOR inhibitor FKBP38, to displace it from mTOR. The contribution of Rheb's regulation of PL-D1 and FKBP38 to mTORC1 activation, relative to Rheb's direct binding to mTOR, remains to be fully defined. The rag GTPases, functioning as obligatory heterodimers, are also required for amino acid regulation of mTORC1. As with amino acid deficiency, however, the inhibitory effect of rag depletion on mTORC1 can be overcome by Rheb overexpression, whereas Rheb depletion obviates rag's ability to activate mTORC1. The rag heterodimer interacts directly with mTORC1 and may direct mTORC1 to the Rheb-containing vesicular compartment in response to amino acid sufficiency, enabling Rheb-GTP activation of mTORC1. The type III phosphatidylinositol kinase also participates in amino acid-dependent mTORC1 activation, although the site of action of its product, 3'OH-phosphatidylinositol, in this process is unclear.
Insights
The mechanistic target of rapamycin complex 1 (mTORC1) controls cell growth. Amino acids regulate mTORC1 via Rheb GTPase and Rag GTPases, influencing Rheb
Area of Science:
- Cellular Biology
- Biochemistry
- Molecular Biology
Background:
- The mechanistic target of rapamycin complex 1 (mTORC1) is a crucial regulator of cell growth, responding to nutrients, growth factors, and cellular stress.
- mTORC1 activity is tightly controlled by various signaling pathways, making its regulatory mechanisms a key area of research.
Purpose of the Study:
- To review the biochemical mechanisms governing mTORC1 kinase activity.
- To emphasize the specific role of amino acids in regulating mTORC1.
- To elucidate the interplay between Rheb GTPase, Rag GTPases, and other factors in mTORC1 activation.
Main Methods:
- Literature review focusing on biochemical and molecular mechanisms of mTORC1 regulation.
- Analysis of studies investigating the roles of Rheb, Rag GTPases, and associated proteins.
- Examination of signaling pathways involving insulin, growth factors, cellular stressors, and amino acids.
Main Results:
- Rheb-GTP is a dominant positive regulator of mTORC1, activated by insulin and growth factors via the tuberous sclerosis complex.
- Amino acids, particularly leucine, regulate mTORC1 by modulating Rheb-GTP's ability to activate mTORC1, not its GTP charging.
- Rag GTPases are essential for amino acid-dependent mTORC1 activation, potentially by facilitating mTORC1 localization to Rheb-containing compartments.
Conclusions:
- mTORC1 regulation is complex, involving direct interactions with Rheb and indirect effects via phospholipase D1 and FKBP38.
- Amino acid sufficiency activates mTORC1 through a pathway involving Rag GTPases and Rheb.
- Further research is needed to fully define the relative contributions of Rheb's various interaction partners and the precise role of type III phosphatidylinositol kinase.
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