School of Medical Sciences, Griffith University, Southport, 4222, Qld, Australia.
Clem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, University of Queensland, Brisbane, 4072, Qld, Australia.
Nat Commun. 2018 Jun 7;9(1):2221. doi: 10.1038/s41467-018-04603-z.
Cell growth and survival depend on a delicate balance between energy production and synthesis of metabolites. Here, we provide evidence that an alternative mitochondrial complex II (CII) assembly, designated as CII, serves as a checkpoint for metabolite biosynthesis under bioenergetic stress, with cells suppressing their energy utilization by modulating DNA synthesis and cell cycle progression. Depletion of CII leads to an imbalance in energy utilization and metabolite synthesis, as evidenced by recovery of the de novo pyrimidine pathway and unlocking cell cycle arrest from the S-phase. In vitro experiments are further corroborated by analysis of paraganglioma tissues from patients with sporadic, SDHA and SDHB mutations. These findings suggest that CII is a core complex inside mitochondria that provides homeostatic control of cellular metabolism depending on the availability of energy.
细胞的生长和存活依赖于能量产生和代谢物合成之间的微妙平衡。在这里,我们提供的证据表明,一种替代的线粒体复合物 II(CII)组装,称为 CII,作为代谢物生物合成的检查点,在生物能量应激下,细胞通过调节 DNA 合成和细胞周期进程来抑制能量利用。CII 的耗竭导致能量利用和代谢物合成的不平衡,这可以通过从头嘧啶途径的恢复和从 S 期释放细胞周期阻滞来证明。体外实验进一步通过分析来自散发、SDHA 和 SDHB 突变的副神经节瘤组织得到证实。这些发现表明,CII 是线粒体内部的核心复合物,根据能量的可用性提供细胞代谢的动态平衡控制。