Mitochondrial SENP2 regulates the assembly of SDH complex under metabolic stress

作者：Liu, Ying; Liu, Kejia; Thorne, Rick F.; Shi, Ronghua; Zhang, Qingyuan^*; Wu, Mian^*; Liu, Lianxin^*

来源：Cell Reports, 2023, 42(2): 112041.

DOI：10.1016/j.celrep.2023.112041

• SUMO
• CANCER
• DESUMOYLATION
• ACETYLATION
• SUMOYLATION
• EXPRESSION
• GLUTAMINE
• PROTEINS
• GLUCOSE

Succinate dehydrogenase (SDH) is a heterotetrameric enzyme complex belonging to the mitochondrial respiratory chain and uniquely links the tricarboxylic acid (TCA) cycle with oxidative phosphorylation. Can-cer-related SDH mutations promote succinate accumulation, which is regarded as an oncometabolite. Post-translational modifications of SDH complex components are known to regulate SDH activity, although the contribution of SUMOylation remains unclear. Here, we show that SDHA is SUMOylated by PIAS3 and deSUMOylated by SENP2, events dictating the assembly and activity of the SDH complex. Moreover, CBP acetylation of SENP2 negatively regulates its deSUMOylation activity. Under glutamine deprivation, CBP levels decrease, and the ensuing SENP2 activation and SDHA deSUMOylation serve to concurrently dampen the TCA cycle and electron transport chain (ETC) activity. Along with succinate accumulation, this mecha-nism avoids excessive reactive oxygen species (ROS) production to promote cancer cell survival. This study elucidates a major function of mitochondrial-localized SENP2 and expands our understanding of the role of SUMOylation in resolving metabolic stress.

• 单位
  1; 哈尔滨医科大学; 郑州大学