| Literature DB >> 28954236 |
Rajarshi Choudhury1, Thomas Bonacci2, Xianxi Wang2, Andrew Truong1, Anthony Arceci3, Yanqiong Zhang2, Christine A Mills1, Jennifer L Kernan1, Pengda Liu4, Michael J Emanuele5.
Abstract
The oncogenic AKT kinase is a key regulator of apoptosis, cell growth, and cell-cycle progression. Despite its important role in proliferation, it remains largely unknown how AKT is mechanistically linked to the cell cycle. We show here that cyclin F, a substrate receptor F-box protein for the SCF (Skp1/Cul1/F-box) family of E3 ubiquitin ligases, is a bona fide AKT substrate. Cyclin F expression oscillates throughout the cell cycle, a rare feature among the 69 human F-box proteins, and all of its known substrates are involved in proliferation. AKT phosphorylation of cyclin F enhances its stability and promotes assembly into productive E3 ligase complexes. Importantly, expression of mutant versions of cyclin F that cannot be phosphorylated by AKT impair cell-cycle entry. Our data suggest that cyclin F transmits mitogen signaling through AKT to the core cell-cycle machinery. This discovery has potential implications for proliferative control in malignancies where AKT is activated.Entities:
Keywords: AKT; SCF ligase; cell cycle; cyclin F; mitogen signaling; phosphorylation; ubiquitin
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Year: 2017 PMID: 28954236 PMCID: PMC5662023 DOI: 10.1016/j.celrep.2017.08.099
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423