Lifespan extension by conditions that inhibit translation in Caenorhabditis elegans
University of California, San Francisco · Institute of Molecular Biology and Biophysics
Abstract
Many conditions that shift cells from states of nutrient utilization and growth to states of cell maintenance extend lifespan. We have carried out a systematic lifespan analysis of conditions that inhibit protein synthesis. We find that reducing the levels of ribosomal proteins, ribosomal-protein S6 kinase or translation-initiation factors increases the lifespan of Caenorhabditis elegans. These perturbations, as well as inhibition of the nutrient sensor target of rapamycin (TOR), which is known to increase lifespan, all increase thermal-stress resistance. Thus inhibiting translation may extend lifespan by shifting cells to physiological states that favor maintenance and repair. Interestingly, different types…
Citation impact
- FWCI
- 11.26
- Percentile
- 100%
- References
- 52
Authors
6- MHMalene HansenCorresponding
University of California, San Francisco
- STStefan Taubert
University of California, San Francisco
- DKDouglas K. Crawford
Institute of Molecular Biology and Biophysics
- NLNataliya Libina
Institute of Molecular Biology and Biophysics
- SLSeung‐Jae Lee
Institute of Molecular Biology and Biophysics
Topics & keywords
- Biology
- Caenorhabditis elegans
- Longevity
- Ribosomal s6 kinase
- Translation (biology)
- Cell biology
- Protein biosynthesis
- Ribosomal protein