Ewald Jennifer C, Kuehne Andreas, Zamboni Nicola, Skotheim Jan M
Department of Biology, Stanford University, Stanford, CA 94305, USA.
Institute of Molecular Systems Biology, ETH Zurich, 8093 Zurich, Switzerland; PhD Program Systems Biology, Life Science Zurich Graduate School, 8057 Zurich, Switzerland.
Mol Cell. 2016 May 19;62(4):532-45. doi: 10.1016/j.molcel.2016.02.017.
Cell division entails a sequence of processes whose specific demands for biosynthetic precursors and energy place dynamic requirements on metabolism. However, little is known about how metabolic fluxes are coordinated with the cell division cycle. Here, we examine budding yeast to show that more than half of all measured metabolites change significantly through the cell division cycle. Cell cycle-dependent changes in central carbon metabolism are controlled by the cyclin-dependent kinase (Cdk1), a major cell cycle regulator, and the metabolic regulator protein kinase A. At the G1/S transition, Cdk1 phosphorylates and activates the enzyme Nth1, which funnels the storage carbohydrate trehalose into central carbon metabolism. Trehalose utilization fuels anabolic processes required to reliably complete cell division. Thus, the cell cycle entrains carbon metabolism to fuel biosynthesis. Because the oscillation of Cdk activity is a conserved feature of the eukaryotic cell cycle, we anticipate its frequent use in dynamically regulating metabolism for efficient proliferation.
细胞分裂涉及一系列过程,这些过程对生物合成前体和能量的特定需求对新陈代谢提出了动态要求。然而,对于代谢通量如何与细胞分裂周期协调,我们知之甚少。在这里,我们研究了芽殖酵母,结果表明,在所有测量的代谢物中,超过一半在细胞分裂周期中发生了显著变化。中心碳代谢中依赖细胞周期的变化由细胞周期蛋白依赖性激酶(Cdk1,一种主要的细胞周期调节因子)和代谢调节蛋白激酶A控制。在G1/S转换期,Cdk1磷酸化并激活Nth1酶,该酶将储存碳水化合物海藻糖导入中心碳代谢。海藻糖的利用为可靠完成细胞分裂所需的合成代谢过程提供能量。因此,细胞周期带动碳代谢为生物合成提供能量。由于Cdk活性的振荡是真核细胞周期的一个保守特征,我们预计它会经常用于动态调节新陈代谢以实现高效增殖。