Regulation of TORC1 by Rag GTPases in nutrient response
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作者:
Kim, Eunjung
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Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USAUniv Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
Kim, Eunjung
[1
,2
]
Goraksha-Hicks, Pankuri
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Univ Minnesota, Dept Genet Cell Biol & Dev, Minneapolis, MN 55455 USAUniv Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
Goraksha-Hicks, Pankuri
[3
]
Li, Li
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Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USAUniv Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
Li, Li
[1
,2
]
Neufeld, Thomas P.
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Univ Minnesota, Dept Genet Cell Biol & Dev, Minneapolis, MN 55455 USAUniv Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
Neufeld, Thomas P.
[3
]
Guan, Kun-Liang
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Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USAUniv Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
Guan, Kun-Liang
[1
,2
]
机构:
[1] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
TORC1 (target of rapamycin complex 1) has a crucial role in the regulation of cell growth and size. A wide range of signals, including amino acids, is known to activate TORC1. Here, we report the identification of Rag GTPases as activators of TORC1 in response to amino acid signals. Knockdown of Rag gene expression suppressed the stimulatory effect of amino acids on TORC1 in Drosophila melanogaster S2 cells. Expression of constitutively active (GTP-bound) Rag in mammalian cells activated TORC1 in the absence of amino acids, whereas expression of dominant-negative Rag blocked the stimulatory effects of amino acids on TORC1. Genetic studies in Drosophila also show that Rag GTPases regulate cell growth, autophagy and animal viability during starvation. Our studies establish a function of Rag GTPases in TORC1 activation in response to amino acid signals.