MNK Controls mTORC1:Substrate Association through Regulation of TELO2 Binding with mTORC1.
The mechanistic target of rapamycin (mTOR) integrates numerous stimuli and coordinates the adaptive response of many cellular processes. To accomplish this, mTOR associates with distinct co-factors that determine its signaling output. While many of these co-factors are known, in many cases their function and regulation remain opaque. The MAPK-interacting kinase (MNK) contributes to rapamycin resistance in cancer cells. Here, we demonstrate that MNK sustains mTORC1 activity following rapamycin treatment and contributes to mTORC1 signaling following T cell activation and growth stimuli in cancer cells. We determine that MNK engages with mTORC1, promotes mTORC1 association with the phosphatidyl inositol 3' kinase-related kinase (PIKK) stabilizer, TELO2, and facilitates mTORC1:substrate binding. Moreover, our data suggest that DEPTOR, the endogenous inhibitor of mTOR, opposes mTORC1:substrate association by preventing TELO2:mTORC1 binding. Thus, MNK orchestrates counterbalancing forces that regulate mTORC1 enzymatic activity.
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Related Subject Headings
- Transcription Factors
- Sirolimus
- Signal Transduction
- Phosphatidylinositol 3-Kinases
- Mitogen-Activated Protein Kinase Kinases
- Mice, Inbred C57BL
- Mice
- Mechanistic Target of Rapamycin Complex 1
- Intracellular Signaling Peptides and Proteins
- Humans
Citation
Published In
DOI
EISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Transcription Factors
- Sirolimus
- Signal Transduction
- Phosphatidylinositol 3-Kinases
- Mitogen-Activated Protein Kinase Kinases
- Mice, Inbred C57BL
- Mice
- Mechanistic Target of Rapamycin Complex 1
- Intracellular Signaling Peptides and Proteins
- Humans