Extension of Life-Span by Loss of CHICO, a <i>Drosophila</i> Insulin Receptor Substrate Protein

David J. Clancy(University College London), David Gems(University College London), Lawrence G. Harshman(University of Nebraska–Lincoln), Sean Oldham(University of Zurich), Hugo Stocker(University of Zurich), Ernst Hafen(University of Zurich), Sally J. Leevers(Ludwig Cancer Research), Linda Partridge(University College London)
Science
April 6, 2001
Cited by 1,439

Abstract

The Drosophila melanogaster gene chico encodes an insulin receptor substrate that functions in an insulin/insulin-like growth factor (IGF) signaling pathway. In the nematode Caenorhabditis elegans, insulin/IGF signaling regulates adult longevity. We found that mutation of chico extends fruit fly median life-span by up to 48% in homozygotes and 36% in heterozygotes. Extension of life-span was not a result of impaired oogenesis in chico females, nor was it consistently correlated with increased stress resistance. The dwarf phenotype of chico homozygotes was also unnecessary for extension of life-span. The role of insulin/IGF signaling in regulating animal aging is therefore evolutionarily conserved.


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