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MDT-15/MED15 permits longevity at low temperature via enhancing lipidostasis and proteostasis.

Dongyeop LeeSeon Woo A AnYoonji JungYasuyo YamaokaYoungjae RyuGrace Ying Shyen GohArshia BeigiJae-Seong YangGyoo Yeol JungDengke K MaChang Man HaStefan TaubertYoungsook LeeSeung-Jae V Lee
Published in: PLoS biology (2019)
Low temperatures delay aging and promote longevity in many organisms. However, the metabolic and homeostatic aspects of low-temperature-induced longevity remain poorly understood. Here, we show that lipid homeostasis regulated by Caenorhabditis elegans Mediator 15 (MDT-15 or MED15), a transcriptional coregulator, is essential for low-temperature-induced longevity and proteostasis. We find that inhibition of mdt-15 prevents animals from living long at low temperatures. We show that MDT-15 up-regulates fat-7, a fatty acid desaturase that converts saturated fatty acids (SFAs) to unsaturated fatty acids (UFAs), at low temperatures. We then demonstrate that maintaining a high UFA/SFA ratio is essential for proteostasis at low temperatures. We show that dietary supplementation with a monounsaturated fatty acid, oleic acid (OA), substantially mitigates the short life span and proteotoxicity in mdt-15(-) animals at low temperatures. Thus, lipidostasis regulated by MDT-15 appears to be a limiting factor for proteostasis and longevity at low temperatures. Our findings highlight the crucial roles of lipid regulation in maintaining normal organismal physiology under different environmental conditions.
Keyphrases
  • fatty acid
  • drosophila melanogaster
  • high glucose
  • diabetic rats
  • gene expression
  • oxidative stress
  • drug induced
  • endothelial cells
  • radiation induced
  • risk assessment
  • climate change
  • heat shock