Journal of Biological Chemistry · 2020 · 56 citations · 39 references
Life SciencesBiochemistryEndocrinologyCell SignalingMetabolismSignal TransductionAdipose TissueInsulin ResistanceLipid MetabolismMetabolic SignalingWeight ManagementMtor Complex 1 SignalingMtor SignalingPhosphatidylinositol 3-Kinase Akt SignalingPhosphatidylinositol 3-Kinase-akt PathwayPhosphatidylinositol 3-Kinase-akt SignalingPhosphoinositide 3-Kinase-akt ActivationPhosphoinositide 3-Kinase-akt SignalingPi3 Kinase-akt Signaling
kinase assay, indicating that mTORC2 may represent the major link between Sestrin2 and AKT. As reported previously, Sestrin2 interacted with mTORC2; however, we found here that this interaction occurs indirectly through GATOR2, a pentameric protein complex that directly interacts with Sestrin2. Deleting or silencing WDR24 (WD repeat domain 24), the GATOR2 component essential for the Sestrin2-GATOR2 interaction, or WDR59, the GATOR2 component essential for the GATOR2-mTORC2 interaction, completely ablated Sestrin2-induced AKT activation. We also noted that Sestrin2 also directly binds to the pleckstrin homology domain of AKT and induces AKT translocation to the plasma membrane. These results uncover a signaling mechanism whereby Sestrin2 activates AKT through GATOR2 and mTORC2.
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Genome engineering using the CRISPR-Cas9 system
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Phosphorylation and Regulation of Akt/PKB by the Rictor-mTOR Complex
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TSC2 is phosphorylated and inhibited by Akt and suppresses mTOR signalling
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