TBC1D13 is a Rab35 specific GAP that plays an important role in glut4 trafficking in adipocytes — ASN Events
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  3. TBC1D13 is a Rab35 specific GAP that plays an important role in glut4 trafficking in adipocytes

TBC1D13 is a Rab35 specific GAP that plays an important role in glut4 trafficking in adipocytes (#71)

Jacqueline Stoeckli 1 , Jonathan R Davey 1 , David G Lambright 2 , David E James 1
  1. Garvan Institute of Medical Research, Darlinghurst, NSW, Australia
  2. UMASS Medical School, Boston, MA, USA
Insulin stimulates glucose transport in adipocytes by triggering translocation of GLUT4 glucose transporters to the plasma membrane (PM) and several Rabs including Rab10 have been implicated in this process. To delineate the molecular regulation of this pathway, we conducted a TBC/RabGAP overexpression screen in adipocytes. This identified TBC1D13 as a potent inhibitor of insulin-stimulated GLUT4 translocation without affecting other trafficking pathways. To determine the potential Rab substrate for TBC1D13 we conducted a yeast two-hybrid screen and found that the GTP bound forms of Rabs 1 and 10 specifically interacted with TBC1D13 but not with eight other TBC proteins. Surprisingly, a comprehensive in vitro screen for TBC1D13 GAP activity revealed Rab35 but not Rab10 as a specific substrate. TBC1D13 also displayed in vivo GAP activity towards Rab35. Overexpression of constitutively active Rab35 but not constitutively active Rab10 reversed the block in insulin-stimulated GLUT4 translocation observed with TBC1D13 overexpression. These studies implicate an important role for Rab35 in insulin-stimulated GLUT4 translocation in adipocytes.