Journal
NATURE CELL BIOLOGY
Volume 21, Issue 9, Pages 1093-+Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/s41556-019-0377-3
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Funding
- Sonnenfeld foundation
- German Research Foundation [TRR186/A08]
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Mechanistic target of rapamycin (mTOR) kinase functions in two multiprotein complexes: lysosomal mTOR complex 1 (mTORC1) and mTORC2 at the plasma membrane. mTORC1 modulates the cell response to growth factors and nutrients by increasing protein synthesis and cell growth, and repressing the autophagy-lysosomal pathway(1-4); however, dysfunction in mTORC1 is implicated in various diseases(3,5,6). mTORC1 activity is regulated by phosphoinositide lipids(7-10). Class I phosphatidylinositol-3-kinase (PI3K)-mediated production of phosphatidylinositol-3,4,5-trisphosphate(6,11) at the plasma membrane stimulates mTORC1 signalling, while local synthesis of phosphatidylinositol-3,4-bisphosphate by starvation-induced recruitment of class II PI3K-beta (PI3KC2-beta) to lysosomes represses mTORC1 activity(12). How the localization and activity of PI3KC2-beta are regulated by mitogens is unknown. We demonstrate that protein kinase N (PKN) facilitates mTORC1 signalling by repressing PI3KC2-beta-mediated phosphatidylinositol-3,4-bisphosphate synthesis downstream of mTORC2. Active PKN2 phosphorylates PI3KC2-beta to trigger PI3KC2-beta complex formation with inhibitory 14-3-3 proteins. Conversely, loss of PKN2 or inactivation of its target phosphorylation site in PI3KC2-beta represses nutrient signalling via mTORC1. These results uncover a mechanism that couples mTORC2-dependent activation of PKN2 to the regulation of mTORC1-mediated nutrient signalling by local lipid signals.
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