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Biochemical and functional characterizations of small GTPase Rheb and TSC2 GAP activity.

Tuberous sclerosis complex (TSC) is a genetic disease caused by a mutation in either the tsc1 or tsc2 tumor suppressor gene. Recent studies have demonstrated that TSC2 displays GAP (GTPase-activating protein) activity specifically towards the small G protein Rheb and inhibits its ability to stimulate the mTOR signaling pathway. Rheb and TSC2 comprise a unique pair of GTPase and GAP, because Rheb has high basal GTP levels and TSC2 does not have the catalytic arginine finger found in Ras-GAP. To investigate the function of TSC2 and Rheb in mTOR signaling, we analyzed the TSC2-stimulated Rheb GTPase activity. We found that Arg15, a residue equivalent to Gly12 in Ras, is important for Rheb to function as a substrate for TSC2 GAP. In addition, we identified asparagine residues essential for TSC2 GAP activity. We demonstrated a novel catalytic mechanism of the TSC2 GAP and Rheb that TSC2 uses a catalytic "asparagine thumb" instead of the arginine finger found in Ras-GAP. Furthermore, we discovered that farnesylation and membrane localization of Rheb is not essential for Rheb to stimulate S6 kinase (S6K) phosphorylation. Analysis of TSC1 binding defective mutants of TSC2 shows that TSC1 is not required for the TSC2 GAP activity but may function as a regulatory component in the TSC1/TSC2 complex. Our data further demonstrate that GAP activity is essential for the cellular function of TSC2 to inhibit S6K phosphorylation.

Pubmed ID: 15340059


  • Li Y
  • Inoki K
  • Guan KL


Molecular and cellular biology

Publication Data

September 1, 2004

Associated Grants


Mesh Terms

  • Binding Sites
  • Cell Line
  • GTPase-Activating Proteins
  • Humans
  • Monomeric GTP-Binding Proteins
  • Mutagenesis, Site-Directed
  • Mutation
  • Neuropeptides
  • Phosphorylation
  • Protein Kinases
  • Protein Prenylation
  • Proteins
  • Recombinant Proteins
  • Repressor Proteins
  • Ribosomal Protein S6 Kinases
  • Signal Transduction
  • TOR Serine-Threonine Kinases
  • Tuberous Sclerosis
  • Tumor Suppressor Proteins