Abstract
The highly conserved target-of-rapamycin (TOR) protein kinases control cell growth in response to nutrients and growth factors. In mammals, TOR has been shown to interact with raptor to relay nutrient signals to downstream translation machinery. We report that in C. elegans, mutations in the genes encoding CeTOR and raptor result in dauer-like larval arrest, implying that CeTOR regulates dauer diapause. The daf-15 (raptor) and let-363 (CeTOR) mutants shift metabolism to accumulate fat, and raptor mutations extend adult life span. daf-15 transcription is regulated by DAF-16, a FOXO transcription factor that is in turn regulated by daf-2 insulin/IGF signaling. This is a new mechanism that regulates the TOR pathway. Thus, DAF-2 insulin/IGF signaling and nutrient signaling converge on DAF-15 (raptor) to regulate C. elegans larval development, metabolism and life span.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Adaptor Proteins, Signal Transducing
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Animals
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Caenorhabditis elegans / growth & development*
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Caenorhabditis elegans / metabolism
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Caenorhabditis elegans Proteins / genetics
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Caenorhabditis elegans Proteins / metabolism*
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Forkhead Transcription Factors
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Insulin / metabolism*
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Molecular Sequence Data
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Phosphotransferases (Alcohol Group Acceptor) / genetics
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Phosphotransferases (Alcohol Group Acceptor) / metabolism*
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Proteins / genetics
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Proteins / metabolism*
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Regulatory-Associated Protein of mTOR
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Signal Transduction / physiology*
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Transcription Factors / metabolism
Substances
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Adaptor Proteins, Signal Transducing
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Caenorhabditis elegans Proteins
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DAF-15 protein, C elegans
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Forkhead Transcription Factors
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Insulin
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Proteins
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RPTOR protein, human
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Regulatory-Associated Protein of mTOR
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Transcription Factors
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daf-16 protein, C elegans
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Phosphotransferases (Alcohol Group Acceptor)
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let-363 protein, C elegans