Ragulator and GATOR1 complexes promote fission yeast growth by attenuating TOR complex 1 through Rag GTPases

被引:31
作者
Chia, Kim Hou [1 ]
Fukuda, Tomoyuki [1 ,2 ]
Sofyantoro, Fajar [1 ,3 ]
Matsuda, Takato [1 ]
Amai, Takamitsu [1 ]
Shiozaki, Kazuhiro [1 ,4 ]
机构
[1] Nara Inst Sci & Technol, Grad Sch Biol Sci, Nara, Japan
[2] Niigata Univ, Grad Sch Med & Dent Sci, Dept Cellular Physiol, Niigata, Japan
[3] Univ Gadjah Mada, Dept Anim Physiol, Fac Biol, Yogyakarta, Indonesia
[4] Univ Calif Davis, Dept Microbiol & Mol Genet, Davis, CA 95616 USA
基金
日本学术振兴会;
关键词
TUBEROUS SCLEROSIS COMPLEX; ACTIVATED PROTEIN-KINASE; AMINO-ACID SUFFICIENCY; SCHIZOSACCHAROMYCES-POMBE; NITROGEN STARVATION; CELL-PROLIFERATION; TSC1-TSC2; COMPLEX; SIGNALING PATHWAY; ARGININE UPTAKE; GAP ACTIVITY;
D O I
10.7554/eLife.30880
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
TOR complex 1 (TORC1) is an evolutionarily conserved protein kinase complex that promotes cellular macromolecular synthesis and suppresses autophagy. Amino-acid-induced activation of mammalian TORC1 is initiated by its recruitment to the RagA/B-RagC/D GTPase heterodimer, which is anchored to lysosomal membranes through the Ragulator complex. We have identified in the model organism Schizosaccharomyces pombe a Ragulator-like complex that tethers the Gtr1-Gtr2 Rag heterodimer to the membranes of vacuoles, the lysosome equivalent in yeasts. Unexpectedly, the Ragulator-Rag complex is not required for the vacuolar targeting of TORC1, but the complex plays a crucial role in attenuating TORC1 activity independently of the Tsc1-Tsc2 complex, a known negative regulator of TORC1 signaling. The GATOR1 complex, which functions as Gtr1 GAP, is essential for the TORC1 attenuation by the Ragulator-Rag complex, suggesting that Gtr1(GDP)-Gtr2 on vacuolar membranes moderates TORC1 signaling for optimal cellular response to nutrients.
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页数:21
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