FBXL20-mediated Vps34 ubiquitination as a p53 controlled checkpoint in regulating autophagy and receptor degradation
Author
Xiao, Juan
Zhang, Tao
Xu, Daichao
Wang, Huibing
Cai, Yu
Jin, Taijie
Liu, Min
Jin, Mingzhi
Wu, Kejia
Yuan, Junying
Published Version
https://doi.org/10.1101/gad.252528.114Metadata
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Xiao, Juan, Tao Zhang, Daichao Xu, Huibing Wang, Yu Cai, Taijie Jin, Min Liu, Mingzhi Jin, Kejia Wu, and Junying Yuan. 2015. “FBXL20-Mediated Vps34 Ubiquitination as a p53 Controlled Checkpoint in Regulating Autophagy and Receptor Degradation.” Genes & Development 29 (2): 184–96. https://doi.org/10.1101/gad.252528.114.Abstract
Vacuolar protein-sorting 34 (Vps34), the catalytic subunit in the class III PtdIns3 (phosphatidylinositol 3) kinase complexes, mediates the production of PtdIns3P, a key intracellular lipid involved in regulating autophagy and receptor degradation. However, the signal transduction pathways by which extracellular signals regulate Vps34 complexes and the downstream cellular mechanisms are not well understood. Here we show that DNA damage-activated mitotic arrest and CDK activation lead to the phosphorylation of Vps34, which provides a signal to promote its ubiquitination and proteasomal degradation mediated by FBXL20 (an F-box protein) and the associated Skp1 (S-phase kinase-associated protein-1)-Cullin1 complex, leading to inhibition of autophagy and receptor endocytosis. Furthermore, we show that the expression of FBXL20 is regulated by p53-dependent transcription. Our study provides a molecular pathway by which DNA damage regulates Vps34 complexes and its downstream mechanisms, including autophagy and receptor endocytosis, through SCF (Skp1-Cul1-F-box)-mediated ubiquitination and degradation. Since the expression of FBXL20 is regulated by p53-dependent transcription, the control of Vps34 ubiquitination and proteasomal degradation by FBXL20 and the associated SCF complex expression provides a novel checkpoint for p53 to regulate autophagy and receptor degradation in DNA damage response.Terms of Use
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