September 13, 2016
Journal Article

FOXO/DAF-16 Activation Slows Down Turnover of the Majority of Proteins in C. elegans

Abstract

Cellular protein quality can be maintained by proteolytic elimination of damaged proteins and replacing them with newly synthesized copies, a process called protein turnover (Ward, 2000). Protein turnover rates have been estimated using SILAC (stable isotope labeling by amino acids in cell culture) in prokaryotes and eukaryotes. The last decade has witnessed a growing interest in the analysis of whole-organism proteome dynamics in metazoans using the same approach (Claydon and Beynon, 2012). In recent work, SILAC was applied to monitor protein synthesis throughout life in adult Caenorhabditis elegans (Vukoti et al., 2015) and to investigate food intake (Gomez-Amaro et al., 2015

Revised: April 13, 2020 | Published: September 13, 2016

Citation

Dhondt I., V.A. Petyuk, H. Cai, L. Vandemeulebroucke, A. Vierstraete, R.D. Smith, and G.G. Depuydt, et al. 2016. FOXO/DAF-16 Activation Slows Down Turnover of the Majority of Proteins in C. elegans. Cell Reports 16, no. 11:3028-3040. PNNL-SA-121059. doi:10.1016/j.celrep.2016.07.088