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Metabolism. Differential regulation of mTORC1 by leucine and glutamine.


ABSTRACT: The mechanistic target of rapamycin (mTOR) complex 1 (mTORC1) integrates environmental and intracellular signals to regulate cell growth. Amino acids stimulate mTORC1 activation at the lysosome in a manner thought to be dependent on the Rag small guanosine triphosphatases (GTPases), the Ragulator complex, and the vacuolar H(+)-adenosine triphosphatase (v-ATPase). We report that leucine and glutamine stimulate mTORC1 by Rag GTPase-dependent and -independent mechanisms, respectively. Glutamine promoted mTORC1 translocation to the lysosome in RagA and RagB knockout cells and required the v-ATPase but not the Ragulator. Furthermore, we identified the adenosine diphosphate ribosylation factor-1 GTPase to be required for mTORC1 activation and lysosomal localization by glutamine. Our results uncover a signaling cascade to mTORC1 activation independent of the Rag GTPases and suggest that mTORC1 is differentially regulated by specific amino acids.

SUBMITTER: Jewell JL 

PROVIDER: S-EPMC4384888 | biostudies-literature | 2015 Jan

REPOSITORIES: biostudies-literature

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Metabolism. Differential regulation of mTORC1 by leucine and glutamine.

Jewell Jenna L JL   Kim Young Chul YC   Russell Ryan C RC   Yu Fa-Xing FX   Park Hyun Woo HW   Plouffe Steven W SW   Tagliabracci Vincent S VS   Guan Kun-Liang KL  

Science (New York, N.Y.) 20150107 6218


The mechanistic target of rapamycin (mTOR) complex 1 (mTORC1) integrates environmental and intracellular signals to regulate cell growth. Amino acids stimulate mTORC1 activation at the lysosome in a manner thought to be dependent on the Rag small guanosine triphosphatases (GTPases), the Ragulator complex, and the vacuolar H(+)-adenosine triphosphatase (v-ATPase). We report that leucine and glutamine stimulate mTORC1 by Rag GTPase-dependent and -independent mechanisms, respectively. Glutamine pro  ...[more]

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