DRAGging amino Acid-mTORC1 signaling by SH3BP4

Young Mi Kim, Do Hyung Kim

Research output: Contribution to journalReview articlepeer-review

9 Scopus citations

Abstract

Mammalian target of rapamycin complex 1 (mTORC1) is a master regulator of cell growth and autophagy. Its activity is regulated by the availability of amino acids and growth factors. The activation of mTORC1 by growth factors, such as insulin and insulin-like growth factor-1 (IGF-1), is mediated by tuberous sclerosis complex (TSC) 1 and 2 and Rheb GTPase. Relative to the growth factor-regulated mTORC1 pathway, the evolutionarily ancient amino acid-mTORC1 pathway remains not yet clearly defined. The amino acid-mTORC1 pathway is mediated by Rag GTPase heterodimers. Several binding proteins of Rag GTPases were discovered in recent studies. Here, we discuss the functions and mechanisms of the newly-identified binders of Rag GTPases. In particular, this review focuses on SH3 binding protein 4 (SH3BP4), the protein recently identifed as a negative regulator of Rag GTPases.

Original languageEnglish (US)
Pages (from-to)1-6
Number of pages6
JournalMolecules and cells
Volume35
Issue number1
DOIs
StatePublished - Jan 2013

Bibliographical note

Funding Information:
We thank the Kim’s lab members for the comments on this review. We apologize to those authors whose works have not been cited in reference due to space limitations. This work was supported by the NIH (DK050456, DK083474 and GM097057).

Keywords

  • Rag GTPases
  • SH3BP4
  • mTOR
  • mTORC1

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