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Cited by 286

The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.

GCN2 sustains mTORC1 suppression upon amino acid deprivation by inducing Sestrin2

Open access
Ye, Jiangbin, Palm, Wilhelm, Peng, Min, King, Bryan, Lindsten, Tullia, Li, Ming O., Koumenis, Constantinos, Thompson, Craig B.·2015·Genes & Development

Abstract

Mammalian cells possess two amino acid-sensing kinases: general control nonderepressible 2 (GCN2) and mechanistic target of rapamycin complex 1 (mTORC1). Their combined effects orchestrate cellular adaptation to amino acid levels, but how their activities are coordinated remains poorly understood. Here, we demonstrate an important link between GCN2 and mTORC1 signaling. Upon deprivation of various amino acids, activated GCN2 up-regulates ATF4 to induce expression of the stress response protein Sestrin2, which is required to sustain repression of mTORC1 by blocking its lysosomal localization. Moreover, Sestrin2 induction is necessary for cell survival during glutamine deprivation, indicating that Sestrin2 is a critical effector of GCN2 signaling that regulates amino acid homeostasis through mTORC1 suppression.

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Metadata

Authors
Ye, J., Palm, W., Peng, M., King, B., Lindsten, T., Li, M. O., Koumenis, C., & Thompson, C. B.
Venue
Genes & Development
Published
2015-11-05
Volume
29
Issue
22
Pages
2331-2336
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
OpenAlex
W2134892089
Cited by
286
References
40
Type
posted content
Language
en
Open access
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CoChat. (2026). Citation check: GCN2 sustains mTORC1 suppression upon amino acid deprivation by inducing Sestrin2. https://app.cochat.ai/papers/10.1101/gad.269324.115
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Ye, J., Palm, W., Peng, M., King, B., Lindsten, T., Li, M. O., Koumenis, C., & Thompson, C. B. (2015). GCN2 sustains mTORC1 suppression upon amino acid deprivation by inducing Sestrin2. Genes & Development. https://doi.org/10.1101/gad.269324.115

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