Phosphoproteomic Analysis Identifies Grb10 as an mTORC1 Substrate That Negatively Regulates Insulin Signaling

Yonghao Yu(Harvard University), Sang-Oh Yoon(Harvard University), George Poulogiannis(Beth Israel Deaconess Medical Center), Qian Yang(Harvard University), Xiaoju Max(Harvard University), Judit Villén(Harvard University), Neil Kubica(Harvard University), Gregory R. Hoffman(Harvard University), Lewis C. Cantley(Beth Israel Deaconess Medical Center), Steven P. Gygi(Harvard University), John Blenis(Harvard University)
Science
June 10, 2011
Cited by 873

Abstract

The evolutionarily conserved serine-threonine kinase mammalian target of rapamycin (mTOR) plays a critical role in regulating many pathophysiological processes. Functional characterization of the mTOR signaling pathways, however, has been hampered by the paucity of known substrates. We used large-scale quantitative phosphoproteomics experiments to define the signaling networks downstream of mTORC1 and mTORC2. Characterization of one mTORC1 substrate, the growth factor receptor-bound protein 10 (Grb10), showed that mTORC1-mediated phosphorylation stabilized Grb10, leading to feedback inhibition of the phosphatidylinositol 3-kinase (PI3K) and extracellular signal-regulated, mitogen-activated protein kinase (ERK-MAPK) pathways. Grb10 expression is frequently down-regulated in various cancers, and loss of Grb10 and loss of the well-established tumor suppressor phosphatase PTEN appear to be mutually exclusive events, suggesting that Grb10 might be a tumor suppressor regulated by mTORC1.


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