Amino acid sufficiency and mTOR regulate p70 S6 kinase and eIF-4E BP1 through a common effector mechanism
What this study shows
Amino acid sufficiency signals through mTOR to p70 S6K and 4E-BP1 via a common effector, first linking nutrients to mTOR.
At a glance
| Evidence type | M Molecular — cells, biochemistry, structure Marked M because it is molecular or in-vitro work (model: CHO cells; in vitro) rather than a whole-organism health-outcome study. That is often exactly where causal biology gets established -- the code says which system the finding was shown in, and nothing about how good the work is. |
| Study type | 5 - Mechanistic / In Vitro |
| Model system | CHO cells; in vitro |
| Journal | The Journal of biological chemistry |
| Year | 1998 |
| Peer reviewed | Yes |
| Record last updated | 2026-10-01 |
| Source | DOI 10.1074/jbc.273.23.14484 · PMID 9603962 |
Extracted findings
These fields were extracted from the paper with AI assistance and have not been checked against the source. Read them as a pointer into the paper, not as curated claims; where they disagree with the curated summary above, the curated summary stands.
| Intervention | Biochemical (amino-acid withdrawal) |
| Target | mTOR / p70 S6K / 4E-BP1 |
| Model | CHO cells; in vitro |
| Effect | Amino-acid sufficiency and mTOR regulate p70 S6K and 4E-BP1 through a common effector mechanism |
In the Atlas
Related topics
Links in the pathway map
- Supports mTORC1 inhibits 4E-BP1
- Supports mTORC1 activates S6K1
More studies on this topic
- Mammalian cell size is controlled by mTOR and its downstream targets S6K1 and 4EBP1/eIF4E (2002)
- mTORC1 phosphorylation sites encode their sensitivity to starvation and rapamycin (2013)
- The mammalian target of rapamycin (mTOR) partner, raptor, binds the mTOR substrates p70 S6 kinase and 4E-BP1 through their TOR signaling (TOS) motif (2003)
- The Bi-steric, mTORC1-Selective Inhibitor, RMC-5552, in Advanced Solid Tumors: A Phase 1 Trial (2025)
Learn the biology
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