The GATOR2–mTORC2 axis mediates Sestrin2-induced AKT Ser/Thr kinase activation

Allison H. Kowalsky, Sim Namkoong, Eric Mettetal, Hwan‐Woo Park, Dubek Kazyken, Diane C. Fingar, Jun Hee Lee

Journal of Biological Chemistry · 2020 · 56 citations · 39 references

DOIFull text

Open access

Concepts

Abstract

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.

References

39