Increased Protein Stability and Decreased Protein Turnover in the Caenorhabditis elegans Ins/IGF-1 daf-2 Mutant.

Depuydt, Geert; Shanmugam, Nilesh; Rasulova, Madina; Dhondt, Ineke; Braeckman, Bart P.

In Caenorhabditis elegans, cellular proteostasis is likely essential for longevity. Autophagy has been shown to be essential for lifespan extension of daf-2 insulin/IGF mutants. Therefore, it can be hypothesized that daf-2 mutants achieve this phenotype by increasing protein turnover. However, such a mechanism would exert a substantial energy cost. By using classical 35S pulse-chase labeling, we observed that protein synthesis and degradation rates are decreased in young adults of the daf-2 insulin/IGF mutants. Although reduction of protein turnover may be energetically favorable, it may lead to accumulation and aggregation of damaged proteins. As this has been shown not to be the case in daf-2 mutants, another mechanism must exist to maintain proteostasis in this strain. We observed that proteins isolated from daf-2 mutants are more soluble in acidic conditions due to increased levels of trehalose. This suggests that trehalose may decrease the potential for protein aggregation and increases proteostasis in the daf-2 mutants. We postulate that daf-2 mutants save energy by decreasing protein turnover rates and instead stabilize their proteome by trehalose.

CAENORHABDITIS elegans; CAENORHABDITIS; PROTEIN stability; PROTEIN metabolism; TREHALOSE; RADIOLABELING; AMINO acid metabolism; ANIMAL experimentation; BIOCHEMISTRY; DISACCHARIDES; GLUTATHIONE; HIGH performance liquid chromatography; LONGEVITY; PHENOMENOLOGY; GENETIC mutation; NEMATODES; PROTEINS; RESEARCH funding; PHENOTYPES

Journals of Gerontology Series A: Biological Sciences & Medical Sciences, 2016, Vol 71, Issue 12, p1553

1079-5006

Academic Journal

10.1093/gerona/glv221