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Regulation of folliculin (the BHD gene product) phosphorylation by Tsc2-mTOR pathway
- Source :
- Biochemical and Biophysical Research Communications. 389:16-21
- Publication Year :
- 2009
- Publisher :
- Elsevier BV, 2009.
-
Abstract
- The Birt-Hogg-Dubé gene (BHD) encodes the tumor suppressor protein folliculin (FLCN). The function of FLCN has recently been implicated in the regulation of rapamycin-sensitive mTOR complex (mTORC1). Reciprocally, the mTORC1-dependent phosphorylation of FLCN was reported. However, precise mechanism of FLCN phosphorylation and functional interaction of FLCN with tuberin, the product of tuberous sclerosis 2 gene (TSC2) which is a negative regulator of mTORC1, are unclear. Here we report that multiple phosphorylation in FLCN are evoked by downregulation of tuberin as well as by Rheb expression. We found that phosphorylation at Ser62 and Ser302 are differently regulated by mTORC1-dependent pathway. Some unknown kinases downstream of tuberin-mTORC1 are thought to directly phosphorylate FLCN. Interestingly, our results also suggest that the complex formation of FLCN with AMPK is modulated by FLCN phosphorylation. These results suggest that FLCN is involved in a novel mechanism of signal transduction downstream of tuberin.
- Subjects :
- Biophysics
P70-S6 Kinase 1
mTORC1
Biochemistry
Gene product
AMP-Activated Protein Kinase Kinases
Cell Line, Tumor
Tuberous Sclerosis Complex 2 Protein
Serine
Animals
Phosphorylation
Folliculin
Molecular Biology
PI3K/AKT/mTOR pathway
Monomeric GTP-Binding Proteins
biology
TOR Serine-Threonine Kinases
Tumor Suppressor Proteins
Neuropeptides
Proteins
Cell Biology
Rats
Cell biology
Amino Acid Substitution
Trans-Activators
Cancer research
biology.protein
Ras Homolog Enriched in Brain Protein
biological phenomena, cell phenomena, and immunity
TSC2
Protein Kinases
Transcription Factors
RHEB
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 389
- Database :
- OpenAIRE
- Journal :
- Biochemical and Biophysical Research Communications
- Accession number :
- edsair.doi.dedup.....4ebd36ddd291c25f379eab9fedcc1f67