Source:http://linkedlifedata.com/resource/pubmed/id/18665908
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2008-10-6
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pubmed:abstractText |
Antagonism between growth-promoting and stress-responsive signaling influences tissue homeostasis and longevity in metazoans. The transcription factor FoxO is central to this regulation, affecting cell proliferation, stress responses, apoptosis, and longevity. Insulin/IGF signaling promotes FoxO phosphorylation, causing its interaction with 14-3-3 molecules. The consequences of this interaction for FoxO-induced biological processes and for the regulation of lifespan in higher organisms remain unclear. Significant complexities in the effects of 14-3-3 proteins on lifespan have been uncovered in Caenorhabditis elegans, suggesting both positive and negative roles for 14-3-3 proteins in the control of aging. Using genetic and biochemical studies, we show here that 14-3-3epsilon antagonizes FoxO function in Drosophila. We find that dFoxO and 14-3-3epsilon proteins interact in vivo and that this interaction is lost in response to oxidative stress. Loss of 14-3-3epsilon results in increased stress-induced apoptosis, growth repression and extended lifespan of flies, phenotypes associated with elevated FoxO function. Our results further show that increased expression of 14-3-3epsilon reverts FoxO-induced growth defects. 14-3-3epsilon thus serves as a central modulator of FoxO activity in the regulation of growth, cell death and longevity in vivo.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/14-3-3 Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Drosophila Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/FOXO protein, Drosophila,
http://linkedlifedata.com/resource/pubmed/chemical/Forkhead Transcription Factors,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Isoforms
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1474-9726
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
688-99
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pubmed:meshHeading |
pubmed-meshheading:18665908-14-3-3 Proteins,
pubmed-meshheading:18665908-Animals,
pubmed-meshheading:18665908-Animals, Genetically Modified,
pubmed-meshheading:18665908-Apoptosis,
pubmed-meshheading:18665908-Drosophila Proteins,
pubmed-meshheading:18665908-Drosophila melanogaster,
pubmed-meshheading:18665908-Female,
pubmed-meshheading:18665908-Forkhead Transcription Factors,
pubmed-meshheading:18665908-Longevity,
pubmed-meshheading:18665908-Male,
pubmed-meshheading:18665908-Oxidative Stress,
pubmed-meshheading:18665908-Protein Isoforms,
pubmed-meshheading:18665908-Retina,
pubmed-meshheading:18665908-Sequence Homology, Amino Acid,
pubmed-meshheading:18665908-Signal Transduction
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pubmed:year |
2008
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pubmed:articleTitle |
14-3-3 Epsilon antagonizes FoxO to control growth, apoptosis and longevity in Drosophila.
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pubmed:affiliation |
Department of Biology, University of Rochester, Rochester, NY 14627, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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