Methionine restriction constrains lipoylation and activates mitochondria for nitrogenic synthesis of amino acids.
Wen FangLiu JiangYibing ZhuSen YangHong QiuJiou ChengQingxi LiangZong-Cai TuCunqi YePublished in: Nature communications (2023)
Methionine restriction (MR) provides metabolic benefits in many organisms. However, mechanisms underlying the MR-induced effect remain incompletely understood. Here, we show in the budding yeast S. cerevisiae that MR relays a signal of S-adenosylmethionine (SAM) deprivation to adapt bioenergetic mitochondria to nitrogenic anabolism. In particular, decreases in cellular SAM constrain lipoate metabolism and protein lipoylation required for the operation of the tricarboxylic acid (TCA) cycle in the mitochondria, leading to incomplete glucose oxidation with an exit of acetyl-CoA and α-ketoglutarate from the TCA cycle to the syntheses of amino acids, such as arginine and leucine. This mitochondrial response achieves a trade-off between energy metabolism and nitrogenic anabolism, which serves as an effector mechanism promoting cell survival under MR.
Keyphrases
- amino acid
- contrast enhanced
- cell death
- magnetic resonance
- reactive oxygen species
- endoplasmic reticulum
- oxidative stress
- insulin resistance
- metabolic syndrome
- small molecule
- adipose tissue
- dendritic cells
- high glucose
- regulatory t cells
- gram negative
- saccharomyces cerevisiae
- cell wall
- protein protein
- stress induced
- immune response