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bioRxiv · 10.1101/2024.02.06.578742

αKG-mediated carnitine synthesis promotes homologous recombination via histone acetylation

Abstract

Homologous recombination (HR) deficiency enhances sensitivity to DNA damaging agents commonly used to treat cancer. In HR-proficient cancers, metabolic mechanisms driving response or resistance to DNA damaging agents remain unclear. Here we identified that depletion of alpha-ketoglutarate (KG) sensitizes HR-proficient cells to DNA damaging agents by metabolic regulation of histone acetylation. KG is required for the activity of KG-dependent dioxygenases (KGDDs), and prior work has shown that changes in KGDD affect demethylases. Using a targeted CRISPR knockout library consisting of 64 KGDDs, we discovered that Trimethyllysine Hydroxylase Epsilon (TMLHE), the first and rate-limiting enzyme in de novo carnitine synthesis, is necessary for proliferation of HR-proficient cells in the presence of DNA damaging agents. Unexpectedly, KG-mediated TMLHE-dependent carnitine synthesis was required for histone acetylation, while histone methylation was affected but dispensable. The increase in histone acetylation via KG-dependent carnitine synthesis promoted HR-mediated DNA repair through site- and substrate-specific histone acetylation. These data demonstrate for the first time that HR-proficiency is mediated through KG directly influencing histone acetylation via carnitine synthesis and provide a metabolic avenue to induce HR-deficiency and sensitivity to DNA damaging agents.

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BibTeXRIS

Uboveja, A., Huang, Z., Buj, R., Amalric, A., Wang, H., Tangudu, N. K., Cole, A. R., Megill, E., Kantner, D., Chatoff, A., Ahmad, H., Marcinkiewicz, M. M., Disharoon, J. A., Graff, S., Dahl, E. S., Hempel, N., Stallaert, W., Sidoli, S., Bitler, B. G., Long, D. T., Snyder, N. W., Aird, K. M.. 2024-02-07. αKG-mediated carnitine synthesis promotes homologous recombination via histone acetylation. https://doi.org/10.1101/2024.02.06.578742

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