ATM Is a Redox Sensor Linking Genome Stability and Carbon Metabolism

Antje Krüger¹ and Markus Ralser^1,2*

¹ Max Planck Institute for Molecular Genetics, Ihnestr 73, 14195 Berlin, Germany.
² Cambridge Systems Biology Centre and Department of Biochemistry, University of Cambridge, 50 Tennis Court Road, Cambridge CB2 1GA, UK.

Abstract: In response to oxidative stress, central carbohydrate metabolism is reconfigured so that the metabolic flux reroutes from glycolysis into the pentose phosphate pathway (PPP), which allows cells to mount an effective response to this cellular stress. The kinase ataxia telangiectasia mutated (ATM) regulates this metabolic shift in mammalian cells. Upon ATM activation, the rate-limiting PPP enzyme glucose 6-phosphate dehydrogenase (G6PDH) formed a complex with heat shock protein 27 that increased G6PDH activity, augmented NADP+ to NADPH reduction, and stimulated nucleotide synthesis. As such, ATM antagonizes the tumor suppressor p53, which is a direct inhibitor of G6PDH and the PPP. In addition to its role in DNA repair and the cell cycle, ATM is thus a component of the eukaryotic redox-sensing system. By linking genome stability, the cell cycle, and carbon catabolism, ATM emerges as a central regulator of cellular metabolism with implications for cancer.

* Corresponding author. E-mail, ralser{at}molgen.mpg.de

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