mTOR Generates an Auto-Amplification Loop by Triggering the beta TrCP- and CK1 alpha-Dependent Degradation of DEPTOR

作者：Duan Shanshan; Skaar Jeffrey R; Kuchay Shafi; Toschi Alfredo; Kanarek Naama; Ben Neriah Yinon; Pagano Michele^*

来源：Molecular Cell, 2011, 44(2): 317-324.

DOI：10.1016/j.molcel.2011.09.005

DEPTOR is a recently identified inhibitor of the mTOR kinase that is highly regulated at the post-translational level. In response to mitogens, we found that DEPTOR was rapidly phosphorylated on three serines in a conserved degron, facilitating binding and ubiquitylation by the F box protein beta TrCP, with consequent proteasomal degradation of DEPTOR. Phosphorylation of the beta TrCP degron in DEPTOR is executed by CK1 alpha after a priming phosphorylation event mediated by either the mTORC1 or mTORC2 complexes. Blocking the beta TrCP-dependent degradation of DEPTOR via beta TrCP knockdown or expression of a stable DEPTOR mutant that is unable to bind beta TrCP results in mTOR inhibition. Our findings reveal that mTOR cooperates with CK1 alpha and beta TrCP to generate an auto-amplification loop to promote its own full activation. Moreover, our results suggest that pharmacologic inhibition of CK1 may be a viable therapeutic option for the treatment of cancers characterized by activation of mTOR-signaling pathways.

• 出版日期2011-10-21