Extended life-span conferred by cotransporter gene mutations in Drosophila.

Aging is genetically determined and environmentally modulated. In a study of longevity in the adult fruit fly, Drosophila melanogaster, we found that five independent P-element insertional mutations in a single gene resulted in a near doubling of the average adult life-span without a decline in fertility or physical activity. Sequence analysis revealed that the product of this gene, named Indy (for I'm not dead yet), is most closely related to a mammalian sodium dicarboxylate cotransporter-a membrane protein that transports Krebs cycle intermediates. Indy was most abundantly expressed in the fat body, midgut, and oenocytes: the principal sites of intermediary metabolism in the fly. Excision of the P element resulted in a reversion to normal life-span. These mutations may create a metabolic state that mimics caloric restriction, which has been shown to extend life-span.

[1]  L. Partridge,et al.  Effects of egg-production and of exposure to males on female survival in Drosophila melanogaster , 1987 .

[2]  U. Berger,et al.  Characterization of a Rat Na+-Dicarboxylate Cotransporter* , 1998, The Journal of Biological Chemistry.

[3]  Andrzej Bartke,et al.  Dwarf mice and the ageing process , 1996, Nature.

[4]  Koutarou D. Kimura,et al.  daf-2, an insulin receptor-like gene that regulates longevity and diapause in Caenorhabditis elegans. , 1997, Science.

[5]  S. Benzer,et al.  Extended life-span and stress resistance in the Drosophila mutant methuselah. , 1998, Science.

[6]  R. S. Sohal,et al.  Relationship between physical activity and life span in the adult housefly, Musca domestica , 1981, Experimental Gerontology.

[7]  A. Pajor Sodium-coupled transporters for Krebs cycle intermediates. , 1999, Annual review of physiology.

[8]  B. Rogina,et al.  Temporal patterns of gene expression in the antenna of the adult Drosophila melanogaster. , 1995, Genetics.

[9]  T. Tully,et al.  latheo, a new gene involved in associative learning and memory in Drosophila melanogaster, identified from P element mutagenesis. , 1992, Genetics.

[10]  L. Partridge,et al.  A cost of mating in female fruitflies , 1989, Nature.

[11]  G. Ruvkun,et al.  A phosphatidylinositol-3-OH kinase family member regulating longevity and diapause in Caenorhabditis elegans , 1996, Nature.

[12]  C. Kenyon,et al.  A C. elegans mutant that lives twice as long as wild type , 1993, Nature.

[13]  G. Ruvkun,et al.  The Fork head transcription factor DAF-16 transduces insulin-like metabolic and longevity signals in C. elegans , 1997, Nature.

[14]  T. Johnson,et al.  Increased life-span of age-1 mutants in Caenorhabditis elegans and lower Gompertz rate of aging. , 1990, Science.

[15]  L. Søndergaard,et al.  Homology between the mammalian liver and the Drosophila fat body. , 1993, Trends in genetics : TIG.

[16]  V. Wigglesworth The Principles of Insect Physiology , 1940 .

[17]  L. Luckinbill,et al.  SELECTION FOR DELAYED SENESCENCE IN DROSOPHILA MELANOGASTER , 1984, Evolution; international journal of organic evolution.

[18]  T. Uemura,et al.  Searching for pattern and mutation in the Drosophila genome with a P-lacZ vector. , 1989, Genes & development.

[19]  R. Weindruch,et al.  Oxidative Stress, Caloric Restriction, and Aging , 1996, Science.

[20]  B. Lakowski,et al.  Determination of Life-Span in Caenorhabditis elegans by Four Clock Genes , 1996, Science.

[21]  R. Reenan,et al.  A-to-I Pre-mRNA Editing in Drosophila Is Primarily Involved in Adult Nervous System Function and Integrity , 2000, Cell.