Kwon Ohman, Kwak Dongoh, Ha Sang Hoon, Jeon Hyeona, Park Mangeun, Chang Yeonho, Suh Pann-Ghill, Ryu Sung Ho
School of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology (POSTECH), Pohang 790-784, Republic of Korea.
Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang 790-784, Republic of Korea.
Cell Signal. 2017 Apr;32:24-35. doi: 10.1016/j.cellsig.2017.01.015. Epub 2017 Jan 13.
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.
雷帕霉素复合物1(mTORC1)的哺乳动物靶点定位于溶酶体是该分子激活的关键步骤。Rag GTP酶对于这种易位至关重要。在此,我们证明Nudix型基序2(NUDT2)是mTORC1激活的一种新型正向调节因子。在NUDT2沉默的细胞中,mTORC1的激活受到损害。从机制上讲,NUDT2与Rag GTP酶结合并控制mTORC1向溶酶体膜的易位。此外,NUDT2依赖性的mTORC1调节对于乳腺癌细胞的增殖至关重要,因为NUDT2沉默的细胞停滞在G0/G1期。综上所述,这些结果表明NUDT2是一种新型的复合物形成增强因子,调节mTORC1-Rag GTP酶信号传导,这对于细胞生长控制至关重要。