mTORC1 promotes metabolic reprogramming by suppression of GSK3-dependent Foxk1 phosphorylation

Published: 19 April 2018| Version 1 | DOI: 10.17632/jt5rg8n3zk.1
Long He


The mammalian Target Of Rapamycin Complex 1 (mTORC1) signaling system plays a critical role in maintenance of cellular homeostasis by sensing and integrating multiple extracellular and intracellular cues. Therefore, uncovering the effectors of mTORC1 signaling is pivotal to understanding its pathophysiological effects. Here we report that the transcription factor forkhead/winged helix family k1 (Foxk1) is a mediator of mTORC1-regulated gene expression. Surprisingly, Foxk1 phosphorylation is increased upon mTORC1 suppression, which elicits 14-3-3 interaction, a reduction of DNA binding and nuclear exclusion. Mechanistically, this occurs by mTORC1-dependent suppression of nuclear signaling by the Foxk1-kinase, Gsk3. This pathway then regulates the expression of multiple genes associated with glycolysis and downstream anabolic pathways directly modulated by Foxk1 and/or by Foxk1-regulated expression of Hif-1. Thus, Foxk1 mediates mTORC1-driven metabolic rewiring and is likely to be critical for metabolic diseases where improper mTORC1 signaling plays an important role.



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