| Literature DB >> 28089905 |
Ohman Kwon1, Dongoh Kwak2, Sang Hoon Ha2, Hyeona Jeon2, Mangeun Park1, Yeonho Chang2, Pann-Ghill Suh3, Sung Ho Ryu4.
Abstract
Lysosomal localization of mammalian target of rapamycin complex 1 (mTORC1) is a critical step for activation of the molecule. Rag GTPases are essential for this translocation. Here, we demonstrate that Nudix-type motif 2 (NUDT2) is a novel positive regulator of mTORC1 activation. Activation of mTORC1 is impaired in NUDT2-silenced cells. Mechanistically, NUDT2 binds to Rag GTPase and controls mTORC1 translocation to the lysosomal membrane. Furthermore, NUDT2-dependent mTORC1 regulation is critical for proliferation of breast cancer cells, as NUDT2-silenced cells arrest in G0/G1 phases. Taken together, these results show that NUDT2 is a novel complex formation enhancing factor regulating mTORC1-Rag GTPase signaling that is crucial for cell growth control.Entities:
Keywords: Cancer cell proliferation; Lysosomal localization; Mammalian target of rapamycin complex 1 (mTORC1); Nudix-type motif 2 (NUDT2); Rag GTPases
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Year: 2017 PMID: 28089905 DOI: 10.1016/j.cellsig.2017.01.015
Source DB: PubMed Journal: Cell Signal ISSN: 0898-6568 Impact factor: 4.315