Glutaminolysis activates Rag-mTORC1 signalling through alpha-ketoglutarate production.
| Evidence tier | D Mechanistic / in vitro / review |
| Study type | 5 - Mechanistic / In Vitro |
| Model system | Mammalian cells |
| Journal | Molecular cell |
| Year | 2012 |
| Peer reviewed | Yes |
| Source | DOI 10.1016/j.molcel.2012.05.043 · PMID 22749528 |
Amino acids control cell growth via activation of the highly conserved kinase TORC1. Glutamine is a particularly important amino acid in cell growth control and metabolism. However, the role of glutamine in TORC1 activation remains poorly defined. Glutamine is metabolized through glutaminolysis to produce alpha-ketoglutarate. We demonstrate that glutamine in combination with leucine activates mammalian TORC1 (mTORC1) by enhancing glutaminolysis and alpha-ketoglutarate production. Inhibition of glutaminolysis prevented GTP loading of RagB and lysosomal translocation and subsequent activation of mTORC1. Constitutively active Rag heterodimer activated mTORC1 in the absence of glutaminolysis. Conversely, enhanced glutaminolysis or a cell-permeable alpha-ketoglutarate analog stimulated lysosomal translocation and activation of mTORC1. Finally, cell growth and autophagy, two processes controlled by mTORC1, were regulated by glutaminolysis. Thus, mTORC1 senses and is activated by glutamine and leucine via glutaminolysis and alpha-ketoglutarate production upstream of Rag. This may provide an explanation for glutamine addiction in cancer cells.
| Intervention | Biochemical/genetic (glutaminolysis) |
| Target | mTORC1 / Rag GTPases (α-ketoglutarate) |
| Model | Mammalian cells |
| Effect | Glutaminolysis (with leucine) activates Rag-mTORC1 signaling via α-ketoglutarate production |