The folliculin tumor suppressor is a GAP for the RagC/D GTPases that signal amino acid levels to mTORC1
What this study shows
FLCN-FNIP is a GAP for RagC/D; GDP-bound RagC/D is required for the Rag heterodimer to bind mTORC1, promoting its lysosomal recruitment and activation by amino acids.
At a glance
| Evidence type | M Molecular — cells, biochemistry, structure Marked M because it is molecular or in-vitro work (model: Mammalian cells) 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 | Mammalian cells |
| Journal | Molecular cell |
| Year | 2013 |
| Peer reviewed | Yes |
| Record last updated | 2026-10-01 |
| Source | DOI 10.1016/j.molcel.2013.09.016 · PMID 24095279 · Free full text (PMC3867817) |
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/genetic (FLCN) |
| Target | FLCN / RagC-RagD / mTORC1 |
| Model | Mammalian cells |
| Effect | The folliculin tumor suppressor is a GAP for RagC/D that signals amino-acid levels to mTORC1 |
In the Atlas
Related topics
More studies on this topic
- Substrate-selective mTORC1 regulation and gene dosage-dependent tissue divergence in Birt-Hogg-Dubé syndrome (2026)
- Structure of the lysosomal mTORC1-TFEB-Rag-Ragulator megacomplex (2023)
- A TBK1/ULK1 signalling axis couples lysosomal stress to TFEB activation. (2026)
- Synergistic role of TFEB/TFE3 and mTORC1 in kidney cystogenesis and tumorigenesis (2026)
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