<i>daf-16</i>/FoxO promotes gluconeogenesis and trehalose synthesis during starvation to support survival.

Abstract

<i>daf-16</i>/FoxO is required to survive starvation in <i>Caenorhabditis elegans</i>, but how <i>daf-16I</i>FoxO promotes starvation resistance is unclear. We show that <i>daf-16</i>/FoxO restructures carbohydrate metabolism by driving carbon flux through the glyoxylate shunt and gluconeogenesis and into synthesis of trehalose, a disaccharide of glucose. Trehalose is a well-known stress protectant, capable of preserving membrane organization and protein structure during abiotic stress. Metabolomic, genetic, and pharmacological analyses confirm increased trehalose synthesis and further show that trehalose not only supports survival as a stress protectant but also serves as a glycolytic input. Furthermore, we provide evidence that metabolic cycling between trehalose and glucose is necessary for this dual function of trehalose. This work demonstrates that <i>daf-16</i>/FoxO promotes starvation resistance by shifting carbon metabolism to drive trehalose synthesis, which in turn supports survival by providing an energy source and acting as a stress protectant.