Abstract

mTOR complex 1 (mTORC1) senses nutrients to mediate anabolic processes within the cell. Exactly how mTORC1 promotes cell growth remains unclear. Here, we identified a novel mTORC1-interacting protein called protein kinase A anchoring protein 8L (AKAP8L). Using biochemical assays, we found that the N-terminal region of AKAP8L binds to mTORC1 in the cytoplasm. Importantly, loss of AKAP8L decreased mTORC1-mediated processes such as translation, cell growth, and cell proliferation. AKAPs anchor protein kinase A (PKA) through PKA regulatory subunits, and we show that AKAP8L can anchor PKA through regulatory subunit Iα. Reintroducing full-length AKAP8L into cells restored mTORC1-regulated processes, whereas reintroduction of AKAP8L missing the N-terminal region that confers the interaction with mTORC1 did not. Our results suggest a multifaceted role for AKAPs in the cell. We conclude that mTORC1 appears to regulate cell growth, perhaps in part through AKAP8L.

Highlights

  • To confirm that AKAP8L-mTOR complex 1 (mTORC1) could interact in cells, HAtagged Raptor and FLAG-tagged AKAP8L were overexpressed in human embryonic kidney 293A (HEK293A) cells (Fig. 1A)

  • We demonstrate that amino acids 63–247 of AKAP8L bind to mTORC1

  • The subcellular localization of this AKAP8L-mTORC1 interaction resides in the cytoplasm

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Summary

Introduction

S6K, 4EBP1, and LARP1 are identified as mTORC1 substrates that regulate protein translation. The PKA catalytic subunits can phosphorylate downstream targets such as cAMP-response element– binding protein (CREB) on Ser-133 [39]. To identify potential mTORC1-interacting proteins, we expressed FLAG-tagged Raptor in human embryonic kidney 293A (HEK293A) cells and analyzed anti-FLAG immunoprecipitates by MS.

Results
Conclusion
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