4.6 Article

Glutamine and asparagine activate mTORC1 independently of Rag GTPases

期刊

JOURNAL OF BIOLOGICAL CHEMISTRY
卷 295, 期 10, 页码 2890-2899

出版社

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.AC119.011578

关键词

amino acid; glutamine; mTOR complex (mTORC); metabolism; signal transduction; ADP-ribosylation factor 1 (Arf1); asparagine; glutamine; mTORC1; Rag GTPase; amino acid sensing; v-ATPase; lysosome; metabolic regulation

资金

  1. CPRIT Scholar Recruitment of First-Time, Tenure-Track Faculty Member Grant [RR150032]
  2. CPRIT High-Impact/High-Risk Research Award [RP160713]
  3. Welch Foundation [I-1927]
  4. 2017 UT Southwestern President's Research Council Distinguished Researcher Award
  5. American Cancer Society (ACS) [ACS-IRG-17-174-13]
  6. National Institutes of Health [R01GM129097-01]

向作者/读者索取更多资源

Nutrient sensing by cells is crucial, and when this sensing mechanism is disturbed, human disease can occur. mTOR complex 1 (mTORC1) senses amino acids to control cell growth, metabolism, and autophagy. Leucine, arginine, and methionine signal to mTORC1 through the well-characterized Rag GTPase signaling pathway. In contrast, glutamine activates mTORC1 through a Rag GTPase?independent mechanism that requires ADP-ribosylation factor 1 (Arf1). Here, using several biochemical and genetic approaches, we show that eight amino acids filter through the Rag GTPase pathway. Like glutamine, asparagine signals to mTORC1 through Arf1 in the absence of the Rag GTPases. Both the Rag-dependent and Rag-independent pathways required the lysosome and lysosomal function for mTORC1 activation. Our results show that mTORC1 is differentially regulated by amino acids through two distinct pathways.

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