4E-BP Extends Lifespan upon Dietary Restriction by Enhancing Mitochondrial Activity in Drosophila
Abstract
Dietary restriction (DR) extends lifespan in multiple species. To examine the mechanisms of lifespan extension upon DR, we assayed genome-wide translational changes in Drosophila. A number of nuclear encoded mitochondrial genes, including those in Complex I and IV of the electron transport chain, showed increased ribosomal loading and enhanced overall activity upon DR. We found that various mitochondrial genes possessed shorter and less structured 5′UTRs, which were important for their enhanced mRNA translation. The translational repressor 4E-BP, the eukaryotic translation initiation factor 4E binding protein, was upregulated upon DR and mediated DR dependent changes in mitochondrial activity and lifespan extension. Inhibition of individual mitochondrial subunits from Complex I and IV diminished the lifespan extension obtained upon DR, reflecting the importance of enhanced mitochondrial function during DR. Our results imply that translational regulation of nuclear-encoded mitochondrial gene expression by 4E-BP plays an important role in lifespan extension upon DR.
Additional Information
© 2009 Elsevier Inc. Received 15 December 2008; revised 25 March 2009; accepted 15 July 2009. Published: October 1, 2009. Available online 1 October 2009. This manuscript is dedicated to the memory of Seymour Benzer, who passed away in the interim between research and publication of the manuscript. We thank David Nicholls, Martin Brand, Judith Campisi, Gordon Lithgow, Nagendra Yadav, Paul Sternberg, Eric Schwarz, Eimear Kenny, and members of the Kapahi and Benzer Labs, for helpful discussions. We would also like to thank the Kimbrell, Lasko, Sonenberg, Tijan, Tower, and Hafen labs for donation of strains and antibodies. This work was funded by grants from the National Institutes of Health (S.B.), a T32 NIH training grant fellowship (A.R.), grants from the Ellison Medical Foundation, American Foundation for aging research, Hillblom foundation, a Nathan Shock Startup award, a gift from the Harold J. and Reta Haynes Family Foundation, and the NIH (RL1AAG032113, 1R21AG028241-01) (P.K.). The microarray work was supported by the Millard and Muriel Jacobs Genetics and Genomics Laboratory at California Institute of Technology.Attached Files
Accepted Version - nihms-136025.pdf
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Additional details
- PMCID
- PMC2759400
- Eprint ID
- 16409
- Resolver ID
- CaltechAUTHORS:20091020-134240373
- Ellison Medical Foundation
- American Foundation for Aging Research
- Hillblom Foundation
- Nathan Shoch Startup Award
- Harold J and Reta Haynes Family Foundation
- RL1AAG032113
- NIH
- 1R21AG028241-01
- NIH
- Millard and Muriel Jacobs Genetics and Genomics Laboratory
- Created
-
2009-10-26Created from EPrint's datestamp field
- Updated
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2021-11-08Created from EPrint's last_modified field