Regulation of cellular growth by the Drosophila target of rapamycin dTOR

Hongbing Zhang, James P. Stallock, Joyce C. Ng, Christoph Reinhard, Thomas P. Neufeld

Research output: Contribution to journalArticlepeer-review

476 Scopus citations

Abstract

The TOR protein kinases (TOR1 and TOR2 in yeast; mTOR/FRAP/RAFT1 in mammals) promote cellular proliferation in response to nutrients and growth factors, but their role in development is poorly understood. Here, we show that the Drosophila TOR homolog dTOR is required cell autonomously for normal growth and proliferation during larval development, and for increases in cellular growth caused by activation of the phosphoinositide 3-kinase (PI3K) signaling pathway. As in mammalian cells, the kinase activity of dTOR is required for growth factor-dependent phosphorylation of p70 S6 kinase (p70S6K) in vitro, and we demonstrate that overexpression of p70S6K in vivo can rescue dTOR mutant animals to viability. Loss of dTOR also results in cellular phenotypes characteristic of amino acid deprivation, including reduced nucleolar size, lipid vesicle aggregation in the larval fat body, and a cell type-specific pattern of cell cycle arrest that can be bypassed by overexpression of the S-phase regulator cyclin E. Our results suggest that dTOR regulates growth during animal development by coupling growth factor signaling to nutrient availability.

Original languageEnglish (US)
Pages (from-to)2712-2724
Number of pages13
JournalGenes and Development
Volume14
Issue number21
DOIs
StatePublished - Nov 1 2000

Keywords

  • Cell cycle
  • Cell growth
  • Drosophila
  • Rapamycin
  • TOR/FRAP

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