The E3 Ligase TRAF6 Regulates Akt Ubiquitination and Activation
The University of Texas MD Anderson Cancer Center · University of Houston · +1 more institution
Abstract
Akt signaling plays a central role in many biological functions, such as cell proliferation and apoptosis. Because Akt (also known as protein kinase B) resides primarily in the cytosol, it is not known how these signaling molecules are recruited to the plasma membrane and subsequently activated by growth factor stimuli. We found that the protein kinase Akt undergoes lysine-63 chain ubiquitination, which is important for Akt membrane localization and phosphorylation. TRAF6 was found to be a direct E3 ligase for Akt and was essential for Akt ubiquitination, membrane recruitment, and phosphorylation upon growth-factor stimulation. The human cancer-associated Akt mutant displayed an increase in Akt ubiquitination,…
Citation impact
- FWCI
- 14.65
- Percentile
- 100%
- References
- 21
Authors
11- WYWei-Lei Yang
The University of Texas MD Anderson Cancer Center, University of Houston
- JWJing Wang
The University of Texas MD Anderson Cancer Center
- CCChia‐Hsin Chan
The University of Texas MD Anderson Cancer Center
- SLSzu-Wei Lee
The University of Texas MD Anderson Cancer Center, University of Houston, The University of Texas Health Science Center at Houston
- ADAlejandro D. Campos
The University of Texas MD Anderson Cancer Center
Topics & keywords
- Protein kinase B
- Ubiquitin ligase
- Phosphorylation
- Cell biology
- PI3K/AKT/mTOR pathway
- Ubiquitin
- Signal transduction
- Chemistry
- Good health and well-being