Abstract
The wild-type Caenorhabditis elegans nematode ages rapidly, undergoing development, senescence, and death in less than 3 weeks. In contrast, mutants with reduced activity of the gene daf-2, a homolog of the insulin and insulin-like growth factor receptors, age more slowly than normal and live more than twice as long. These mutants are active and fully fertile and have normal metabolic rates. The life-span extension caused by daf-2 mutations requires the activity of the gene daf-16. daf-16 appears to play a unique role in life-span regulation and encodes a member of the hepatocyte nuclear factor 3 (HNF-3)/forkhead family of transcriptional regulators. In humans, insulin down-regulates the expression of certain genes by antagonizing the activity of HNF-3, raising the possibility that aspects of this regulatory system have been conserved.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Aging / genetics
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Amino Acid Sequence
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Animals
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Base Sequence
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Caenorhabditis elegans / genetics*
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Caenorhabditis elegans / physiology
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Caenorhabditis elegans Proteins*
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Cloning, Molecular
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DNA, Complementary
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Forkhead Transcription Factors
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Genes, Helminth
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Humans
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Insulin / physiology
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Longevity / genetics
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Molecular Sequence Data
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Mutation
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Nuclear Proteins / genetics
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Phenotype
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Receptor, Insulin / genetics
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Receptor, Insulin / physiology
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Sequence Alignment
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Somatomedins / physiology
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Transcription Factors / chemistry
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Transcription Factors / genetics*
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Transcription Factors / physiology*
Substances
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Caenorhabditis elegans Proteins
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DNA, Complementary
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Forkhead Transcription Factors
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Insulin
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Nuclear Proteins
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Somatomedins
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Transcription Factors
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daf-16 protein, C elegans
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DAF-2 protein, C elegans
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Receptor, Insulin