PIP4Ks Suppress Insulin Signaling Through a Catalytic-Independent Mechanism

Wang, D. G.; Paddock, M. N.; Lundquist, M. R.; Sun, J. Y.; Mashadova, O.; Amadiume, S.; Bumpus, T. W.; Hodakoski, C.; Hopkins, B. D.; Fine, M.; Hill, A.; Yang, T. J.; Baskin, J. M.; Dow, L. E.; Cantley, L. C.

doi:10.1101/370544

bioRxiv · 10.1101/370544

PIP4Ks Suppress Insulin Signaling Through a Catalytic-Independent Mechanism

Wang, D. G.·Paddock, M. N.·Lundquist, M. R.·Sun, J. Y.·Mashadova, O.·Amadiume, S.·Bumpus, T. W.·Hodakoski, C.·Hopkins, B. D.·Fine, M.·Hill, A.·Yang, T. J.·Baskin, J. M.·Dow, L. E.·Cantley, L. C.

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Abstract

Insulin stimulates conversion of phosphatidylinositol-4,5-bisphosphate (PI(4,5)P2) to phosphatidylinositol-3,4,5-trisphosphate (PI(3,4,5)P3), which mediates downstream cellular responses. PI(4,5)P2 is produced by phosphatidylinositol-4-phosphate 5-kinases (PIP5Ks) and byphosphatidylinositol-5-phosphate 4-kinases (PIP4Ks). Here we show that deletion of the three genes that encode PIP4Ks (PIP4K2A, PIP4K2B and PIP4K2C) in vitro results in a paradoxical increase in PI(4,5)P2 and a subsequent increase in insulin-stimulated production of PI(3,4,5)P3. Surprisingly, reintroduction of either wild-type or kinase-dead forms of the PIP4Ks restored cellular PI(4,5)P2 levels and insulin stimulation of the PI3K pathway. These effects are explained by an increase in PIP5K activity upon deletion of PIP4Ks, which we demonstrate can suppress PIP5K activity in vitro through a direct binding interaction. Collectively, our work reveals an important non-catalytic function of PIP4Ks in suppressing PIP5K-mediated PI(4,5)P2 synthesis and insulin-dependent conversion to PI(3,4,5)P3 by PI3K enzymes and suggests that pharmacological depletion of PIP4K enzymes using emerging degrader technologies could represent a novel strategy for stimulating insulin signaling.

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Wang, D. G., Paddock, M. N., Lundquist, M. R., Sun, J. Y., Mashadova, O., Amadiume, S., Bumpus, T. W., Hodakoski, C., Hopkins, B. D., Fine, M., Hill, A., Yang, T. J., Baskin, J. M., Dow, L. E., Cantley, L. C.. 2018-07-20. PIP4Ks Suppress Insulin Signaling Through a Catalytic-Independent Mechanism. https://doi.org/10.1101/370544

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