4.6 Review Book Chapter

Amino Acid Signaling in TOR Activation

期刊

ANNUAL REVIEW OF BIOCHEMISTRY, VOL 80
卷 80, 期 -, 页码 1001-1032

出版社

ANNUAL REVIEWS
DOI: 10.1146/annurev-biochem-062209-094414

关键词

Rag GTPase/Gtr complex; TORC; TSC; Rheb; amino acids; rapamycin

资金

  1. NCI NIH HHS [CA108941, R01 CA108941] Funding Source: Medline
  2. NIGMS NIH HHS [GM62694, R01 GM051586, GM51586] Funding Source: Medline
  3. NATIONAL CANCER INSTITUTE [R01CA108941] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM051586, R01GM062694] Funding Source: NIH RePORTER

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The target of rapamycin (TOR) is a central cell growth regulator conserved from yeast to mammals. Uncontrolled TOR activation is commonly observed in human cancers. TOR forms two distinct structural and functional complexes, TORC1 and TORC2. TORC1 promotes cell growth and cell size by stimulating protein synthesis. A wide range of signals, including nutrients, energy levels, and growth factors, are known to control TORC1 activity. Among them, amino acids (AA) not only potently activate TORC1 but are also required for TORC1 activation by other stimuli, such as growth factors. The mechanisms of growth factors and cellular energy status in activating TORC1 have been well elucidated, whereas the molecular basis of AA signaling is just emerging. Recent advances in the role of AA signaling on TORC1 activation have revealed key components, including the Rag GTPases, protein kinases, nutrient transporters, and the intracellular trafficking machinery, in relaying AA signals to TORC1 activation.

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