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Sin1 phosphorylation impairs mTORC2 complex integrity and inhibits downstream Akt signalling to suppress tumorigenesis

Authors
 Pengda Liu  ;  Wenjian Gan  ;  Hiroyuki Inuzuka  ;  Adam S Lazorchak  ;  Daming Gao  ;  Omotooke Arojo  ;  Dou Liu  ;  Lixin Wan  ;  Bo Zhai  ;  Yonghao Yu  ;  Min Yuan  ;  Byeong Mo Kim  ;  Shavali Shaik  ;  Suchithra Menon  ;  Steven P. Gygi  ;  Tae Ho Lee  ;  John M Asara  ;  Brendan D. Manning  ;  John Blenis  ;  Bing Su  ;  Wenyi Wei 
Citation
 NATURE CELL BIOLOGY, Vol.15(11) : 1340-1350, 2013 
Journal Title
 NATURE CELL BIOLOGY 
ISSN
 1465-7392 
Issue Date
2013
MeSH
Adaptor Proteins, Signal Transducing/genetics ; Adaptor Proteins, Signal Transducing/metabolism* ; Carcinogenesis* ; Humans ; Mechanistic Target of Rapamycin Complex 2 ; Multiprotein Complexes/metabolism* ; Mutation ; Phosphorylation ; Proto-Oncogene Proteins c-akt/metabolism* ; Signal Transduction* ; TOR Serine-Threonine Kinases/metabolism*
Abstract
The mechanistic target of rapamycin (mTOR) functions as a critical regulator of cellular growth and metabolism by forming multi-component, yet functionally distinct complexes mTORC1 and mTORC2. Although mTORC2 has been implicated in mTORC1 activation, little is known about how mTORC2 is regulated. Here we report that phosphorylation of Sin1 at Thr 86 and Thr 398 suppresses mTORC2 kinase activity by dissociating Sin1 from mTORC2. Importantly, Sin1 phosphorylation, triggered by S6K or Akt, in a cellular context-dependent manner, inhibits not only insulin- or IGF-1-mediated, but also PDGF- or EGF-induced Akt phosphorylation by mTORC2, demonstrating a negative regulation of mTORC2 independent of IRS-1 and Grb10. Finally, a cancer-patient-derived Sin1-R81T mutation impairs Sin1 phosphorylation, leading to hyper-activation of mTORC2 by bypassing this negative regulation. Together, our results reveal a Sin1-phosphorylation-dependent mTORC2 regulation, providing a potential molecular mechanism by which mutations in the mTORC1-S6K-Sin1 signalling axis might cause aberrant hyper-activation of the mTORC2-Akt pathway, which facilitates tumorigenesis.
Files in This Item:
T201306077.pdf Download
DOI
10.1038/ncb2860
Appears in Collections:
5. Research Institutes (연구소) > Yonsei Integrative Research Institute for Cerebral & Cardiovascular Disease (뇌심혈관질환융합연구사업단) > 1. Journal Papers
Yonsei Authors
Kim, Byeong Mo(김병모) ORCID logo https://orcid.org/0000-0002-0582-3132
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/158412
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