Cell Biology Unit, Medical Research Council Laboratory for Molecular Cell Biology, and Department of Cell and Developmental Biology, University College London, Gower Street, London WC1E 6BT, UK.
Science. 2011 Nov 11;334(6057):802-5. doi: 10.1126/science.1211908.
With its high-energy phosphate bonds, adenosine triphosphate (ATP) is the main intracellular energy carrier. It also functions in most signaling pathways, as a phosphate donor or a precursor for cyclic adenosine monophosphate. We show here that inositol pyrophosphates participate in the control of intracellular ATP concentration. Yeasts devoid of inositol pyrophosphates have dysfunctional mitochondria but, paradoxically, contain four times as much ATP because of increased glycolysis. We demonstrate that inositol pyrophosphates control the activity of the major glycolytic transcription factor GCR1. Thus, inositol pyrophosphates regulate ATP concentration by altering the glycolytic/mitochondrial metabolic ratio. Metabolic reprogramming through inositol pyrophosphates is an evolutionary conserved mechanism that is also preserved in mammalian systems.
三磷酸腺苷(ATP)通过高能磷酸键成为细胞内主要的能量载体。它在大多数信号通路中也发挥作用,作为磷酸供体或环状单磷酸腺苷的前体。我们在这里表明,肌醇六磷酸参与了细胞内 ATP 浓度的控制。缺乏肌醇六磷酸的酵母线粒体功能失调,但由于糖酵解增加,它们的 ATP 含量却增加了四倍。我们证明肌醇六磷酸控制主要糖酵解转录因子 GCR1 的活性。因此,肌醇六磷酸通过改变糖酵解/线粒体代谢比率来调节 ATP 浓度。通过肌醇六磷酸进行的代谢重编程是一种进化上保守的机制,在哺乳动物系统中也得到了保留。