A-kinase anchoring protein 8L interacts with mTORC1 and promotes cell growth

J Biol Chem. 2020 Jun 5;295(23):8096-8105. doi: 10.1074/jbc.AC120.012595. Epub 2020 Apr 20.

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.

Keywords: A-kinase anchoring protein (AKAP); AKAP8L; anabolic pathway; cAMP signaling; cell biology; cell proliferation; cell size; mRNA translation; mTOR complex (mTORC); mTORC1; nutrient sensing; protein kinase A (PKA); protein synthesis; scaffolding protein.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Proliferation
  • DNA-Binding Proteins / deficiency
  • DNA-Binding Proteins / metabolism*
  • HEK293 Cells
  • Humans
  • Intracellular Signaling Peptides and Proteins / deficiency
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Mechanistic Target of Rapamycin Complex 1 / metabolism*
  • Nuclear Proteins / deficiency
  • Nuclear Proteins / metabolism*

Substances

  • AKAP8L protein, human
  • DNA-Binding Proteins
  • Intracellular Signaling Peptides and Proteins
  • Nuclear Proteins
  • Mechanistic Target of Rapamycin Complex 1