
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.
DNA Replication, Saccharomyces cerevisiae Proteins, Time Factors, Cell Cycle, Trehalose, Saccharomyces cerevisiae, Cyclic AMP-Dependent Protein Kinases, G1 Phase Cell Cycle Checkpoints, Carbon, Enzyme Activation, CDC2 Protein Kinase, Trehalase, Phosphorylation, DNA, Fungal, Energy Metabolism, CDC28 Protein Kinase, S cerevisiae, Cell Proliferation, Signal Transduction
DNA Replication, Saccharomyces cerevisiae Proteins, Time Factors, Cell Cycle, Trehalose, Saccharomyces cerevisiae, Cyclic AMP-Dependent Protein Kinases, G1 Phase Cell Cycle Checkpoints, Carbon, Enzyme Activation, CDC2 Protein Kinase, Trehalase, Phosphorylation, DNA, Fungal, Energy Metabolism, CDC28 Protein Kinase, S cerevisiae, Cell Proliferation, Signal Transduction
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