The mTORC1 Signaling Network Senses Changes in Cellular Purine Nucleotide Levels
Summary: Mechanistic (or mammalian) target of rapamycin complex 1 (mTORC1) integrates signals from growth factors and nutrients to control biosynthetic processes, including protein, lipid, and nucleic acid synthesis. We find that the mTORC1 pathway is responsive to changes in purine nucleotides in a...
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doaj-2f396a16f2994d80bba511cc912618782020-11-25T01:52:00ZengElsevierCell Reports2211-12472017-10-0121513311346The mTORC1 Signaling Network Senses Changes in Cellular Purine Nucleotide LevelsGerta Hoxhaj0James Hughes-Hallett1Rebecca C. Timson2Erika Ilagan3Min Yuan4John M. Asara5Issam Ben-Sahra6Brendan D. Manning7Department of Genetics and Complex Diseases, Harvard T. H. Chan School of Public Health, Boston, MA, USADepartment of Genetics and Complex Diseases, Harvard T. H. Chan School of Public Health, Boston, MA, USADepartment of Genetics and Complex Diseases, Harvard T. H. Chan School of Public Health, Boston, MA, USADepartment of Genetics and Complex Diseases, Harvard T. H. Chan School of Public Health, Boston, MA, USADivision of Signal Transduction, Beth Israel Deaconess Medical Center, Boston, MA, USA; Department of Medicine, Harvard Medical School, Boston, MA, USADivision of Signal Transduction, Beth Israel Deaconess Medical Center, Boston, MA, USA; Department of Medicine, Harvard Medical School, Boston, MA, USAFeinberg School of Medicine, Northwestern University, Chicago, IL, USADepartment of Genetics and Complex Diseases, Harvard T. H. Chan School of Public Health, Boston, MA, USA; Corresponding authorSummary: Mechanistic (or mammalian) target of rapamycin complex 1 (mTORC1) integrates signals from growth factors and nutrients to control biosynthetic processes, including protein, lipid, and nucleic acid synthesis. We find that the mTORC1 pathway is responsive to changes in purine nucleotides in a manner analogous to its sensing of amino acids. Depletion of cellular purines, but not pyrimidines, inhibits mTORC1, and restoration of intracellular adenine nucleotides via addition of exogenous purine nucleobases or nucleosides acutely reactivates mTORC1. Adenylate sensing by mTORC1 is dependent on the tuberous sclerosis complex (TSC) protein complex and its regulation of Rheb upstream of mTORC1, but independent of energy stress and AMP-activated protein kinase (AMPK). Even though mTORC1 signaling is not acutely sensitive to changes in intracellular guanylates, long-term depletion of guanylates decreases Rheb protein levels. Our findings suggest that nucleotide sensing, like amino acid sensing, enables mTORC1 to tightly coordinate nutrient availability with the synthesis of macromolecules, such as protein and nucleic acids, produced from those nutrients. : mTORC1 integrates signals from growth factors and nutrients to coordinately control macromolecular synthesis. Hoxhaj et al. identify intracellular purine nucleotides as an upstream regulatory input into the mTORC1 pathway. Acutely, mTORC1 senses adenylates in a manner dependent on the TSC complex, while prolonged guanylate depletion results in reduced Rheb levels. Keywords: mTOR, nutrient sensing, purine, nucleotides, ATP, GTP, tuberous sclerosis complex, Rheb, Rag GTPases, AMPKhttp://www.sciencedirect.com/science/article/pii/S2211124717314614 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Gerta Hoxhaj James Hughes-Hallett Rebecca C. Timson Erika Ilagan Min Yuan John M. Asara Issam Ben-Sahra Brendan D. Manning |
spellingShingle |
Gerta Hoxhaj James Hughes-Hallett Rebecca C. Timson Erika Ilagan Min Yuan John M. Asara Issam Ben-Sahra Brendan D. Manning The mTORC1 Signaling Network Senses Changes in Cellular Purine Nucleotide Levels Cell Reports |
author_facet |
Gerta Hoxhaj James Hughes-Hallett Rebecca C. Timson Erika Ilagan Min Yuan John M. Asara Issam Ben-Sahra Brendan D. Manning |
author_sort |
Gerta Hoxhaj |
title |
The mTORC1 Signaling Network Senses Changes in Cellular Purine Nucleotide Levels |
title_short |
The mTORC1 Signaling Network Senses Changes in Cellular Purine Nucleotide Levels |
title_full |
The mTORC1 Signaling Network Senses Changes in Cellular Purine Nucleotide Levels |
title_fullStr |
The mTORC1 Signaling Network Senses Changes in Cellular Purine Nucleotide Levels |
title_full_unstemmed |
The mTORC1 Signaling Network Senses Changes in Cellular Purine Nucleotide Levels |
title_sort |
mtorc1 signaling network senses changes in cellular purine nucleotide levels |
publisher |
Elsevier |
series |
Cell Reports |
issn |
2211-1247 |
publishDate |
2017-10-01 |
description |
Summary: Mechanistic (or mammalian) target of rapamycin complex 1 (mTORC1) integrates signals from growth factors and nutrients to control biosynthetic processes, including protein, lipid, and nucleic acid synthesis. We find that the mTORC1 pathway is responsive to changes in purine nucleotides in a manner analogous to its sensing of amino acids. Depletion of cellular purines, but not pyrimidines, inhibits mTORC1, and restoration of intracellular adenine nucleotides via addition of exogenous purine nucleobases or nucleosides acutely reactivates mTORC1. Adenylate sensing by mTORC1 is dependent on the tuberous sclerosis complex (TSC) protein complex and its regulation of Rheb upstream of mTORC1, but independent of energy stress and AMP-activated protein kinase (AMPK). Even though mTORC1 signaling is not acutely sensitive to changes in intracellular guanylates, long-term depletion of guanylates decreases Rheb protein levels. Our findings suggest that nucleotide sensing, like amino acid sensing, enables mTORC1 to tightly coordinate nutrient availability with the synthesis of macromolecules, such as protein and nucleic acids, produced from those nutrients. : mTORC1 integrates signals from growth factors and nutrients to coordinately control macromolecular synthesis. Hoxhaj et al. identify intracellular purine nucleotides as an upstream regulatory input into the mTORC1 pathway. Acutely, mTORC1 senses adenylates in a manner dependent on the TSC complex, while prolonged guanylate depletion results in reduced Rheb levels. Keywords: mTOR, nutrient sensing, purine, nucleotides, ATP, GTP, tuberous sclerosis complex, Rheb, Rag GTPases, AMPK |
url |
http://www.sciencedirect.com/science/article/pii/S2211124717314614 |
work_keys_str_mv |
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