Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Long-Lived Drosophila with Overexpressed dFOXO in Adult Fat Body
Maria E. Giannakou,1Martin Goss,1Martin A. Jünger,2Ernst Hafen,2Sally J. Leevers,3Linda Partridge1*
Reduced activity of the insulin/insulin-like growth factor signaling(IIS) pathway increases life-span in diverse organisms. We investigatedthe timing of the effect of reduced IIS on life-span and therole of a potential target tissue, the fat body. We overexpresseddFOXO, a downstream effector of IIS, in the adult Drosophilafat body, which increased life-span and reduced fecundity offemales but had no effect on male life-span. The role of FOXOtranscription factors and the adipose tissue are therefore evolutionarilyconserved in the regulation of aging, and reduction of IIS inthe adult is sufficient to mediate its effects on life-spanand fecundity.
1 Department of Biology, University College London, Darwin Building, Gower Street, London WC1E 6BT, UK. 2 Zoologisches Institut, Universität Zürich, Winterthurerstraße 190, CH-8057, Zürich, Switzerland. 3 Growth Regulation Laboratory, Cancer Research UK, London Research Institute, Post Office Box 123, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.
* To whom correspondence should be addressed. E-mail: L.Partridge{at}ucl.ac.uk
The editors suggest the following Related Resources on Science sites:
In Science Magazine
TECHNICAL COMMENTS
Marc Tatar (4 February 2005) Science307 (5710), 675a.
[DOI: 10.1126/science.1104721] |Full Text »|PDF »
TECHNICAL COMMENTS
Maria E. Giannakou, Martin Goss, Martin A. Jünger, Ernst Hafen, Sally J. Leevers, and Linda Partridge (4 February 2005) Science307 (5710), 675b.
[DOI: 10.1126/science.1104733] |Full Text »|PDF »
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
The GAL4 System: A Versatile Toolkit for Gene Expression in Drosophila.
T. D. Southall, D. A. Elliott, and A. H. Brand (2008)
CSH Protocols
2008, pdb.top49
|Abstract »|Full Text »
Insulin signaling is involved in the regulation of worker division of labor in honey bee colonies.
S. A. Ament, M. Corona, H. S. Pollock, and G. E. Robinson (2008)
PNAS
105, 4226-4231
|Abstract »|Full Text »|PDF »
Signaling networks in aging.
E. L. Greer and A. Brunet (2008)
J. Cell Sci.
121, 407-412
|Full Text »|PDF »
Forkhead Transcription Factors and Cardiovascular Biology.
DNA damage, cellular senescence and organismal ageing: causal or correlative?.
J.-H. Chen, C. N. Hales, and S. E. Ozanne (2007)
Nucleic Acids Res.
35, 7417-7428
|Abstract »|Full Text »|PDF »
The Energy Sensor AMP-activated Protein Kinase Directly Regulates the Mammalian FOXO3 Transcription Factor.
E. L. Greer, P. R. Oskoui, M. R. Banko, J. M. Maniar, M. P. Gygi, S. P. Gygi, and A. Brunet (2007)
J. Biol. Chem.
282, 30107-30119
|Abstract »|Full Text »|PDF »
FOXO and insulin signaling regulate sensitivity of the circadian clock to oxidative stress.
X. Zheng, Z. Yang, Z. Yue, J. D. Alvarez, and A. Sehgal (2007)
PNAS
104, 15899-15904
|Abstract »|Full Text »|PDF »
Expression of dominant-negative Dmp53 in the adult fly brain inhibits insulin signaling.
J. H. Bauer, C. Chang, S. N. S. Morris, S. Hozier, S. Andersen, J. S. Waitzman, and S. L. Helfand (2007)
PNAS
104, 13355-13360
|Abstract »|Full Text »|PDF »
Temporal and spatial transcriptional profiles of aging in Drosophila melanogaster.
M. Zhan, H. Yamaza, Y. Sun, J. Sinclair, H. Li, and S. Zou (2007)
Genome Res.
17, 1236-1243
|Abstract »|Full Text »|PDF »
The emerging role of FOXO transcription factors in pancreatic {beta} cells.
Coordinated multitissue transcriptional and plasma metabonomic profiles following acute caloric restriction in mice.
C. Selman, N. D. Kerrison, A. Cooray, M. D. W. Piper, S. J. Lingard, R. H. Barton, E. F. Schuster, E. Blanc, D. Gems, J. K. Nicholson, et al. (2006)
Physiol Genomics
27, 187-200
|Abstract »|Full Text »|PDF »
Increased Rheb-TOR signaling enhances sensitivity of the whole organism to oxidative stress.
Peroxisome Proliferator-Activated Receptor {gamma} Coactivator 1 in Caloric Restriction and Other Models of Longevity.
J. C. Corton and H. M. Brown-Borg (2005)
J. Gerontol. A Biol. Sci. Med. Sci.
60, 1494-1509
|Abstract »|Full Text »|PDF »
Regulation of Oxidative Stress by the Anti-aging Hormone Klotho.
M. Yamamoto, J. D. Clark, J. V. Pastor, P. Gurnani, A. Nandi, H. Kurosu, M. Miyoshi, Y. Ogawa, D. H. Castrillon, K. P. Rosenblatt, et al. (2005)
J. Biol. Chem.
280, 38029-38034
|Abstract »|Full Text »|PDF »
Metabolism, ubiquinone synthesis, and longevity.
H. Aguilaniu, J. Durieux, and A. Dillin (2005)
Genes & Dev.
19, 2399-2406
|Full Text »|PDF »
4E-BP functions as a metabolic brake used under stress conditions but not during normal growth.
A. A. Teleman, Y.-W. Chen, and S. M. Cohen (2005)
Genes & Dev.
19, 1844-1848
|Abstract »|Full Text »|PDF »
Starvation and oxidative stress resistance in Drosophila are mediated through the eIF4E-binding protein, d4E-BP.
G. Tettweiler, M. Miron, M. Jenkins, N. Sonenberg, and P. F. Lasko (2005)
Genes & Dev.
19, 1840-1843
|Abstract »|Full Text »|PDF »
Counting the Calories: The Role of Specific Nutrients in Extension of Life Span by Food Restriction.
M. D. W. Piper, W. Mair, and L. Partridge (2005)
J. Gerontol. A Biol. Sci. Med. Sci.
60, 549-555
|Abstract »|Full Text »|PDF »
Phosphorylation of p66Shc and forkhead proteins mediates A{beta} toxicity.
W. W. Smith, D. D. Norton, M. Gorospe, H. Jiang, S. Nemoto, N. J. Holbrook, T. Finkel, and J. W. Kusiak (2005)
J. Cell Biol.
169, 331-339
|Abstract »|Full Text »|PDF »
Estrogen, Insulin, and Dietary Signals Cooperatively Regulate Longevity Signals to Enhance Resistance to Oxidative Stress in Mice.
T. Baba, T. Shimizu, Y.-i. Suzuki, M. Ogawara, K.-i. Isono, H. Koseki, H. Kurosawa, and T. Shirasawa (2005)
J. Biol. Chem.
280, 16417-16426
|Abstract »|Full Text »|PDF »
Longer lifespan, altered metabolism, and stress resistance in Drosophila from ablation of cells making insulin-like ligands.
S. J. Broughton, M. D. W. Piper, T. Ikeya, T. M. Bass, J. Jacobson, Y. Driege, P. Martinez, E. Hafen, D. J. Withers, S. J. Leevers, et al. (2005)
PNAS
102, 3105-3110
|Abstract »|Full Text »|PDF »
Comment on "Long-Lived Drosophila with Overexpressed dFOXO in Adult Fat Body".