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

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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