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bioRxiv · 10.1101/2022.12.28.522149

Dynamic protein deacetylation is a limited carbon source for acetyl-CoA-dependent metabolism

Soaita, I.·Megill, E.·Kantner, D.·Chatoff, A.·Arany, Z.·Snyder, N. W.·Wellen, K. E.·Trefely, S. W.
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Abstract

The ability of cells to store and rapidly mobilize energy reserves in response to nutrient availability is essential for survival. Breakdown of carbon stores produces acetyl-coenzyme-A (acetyl-CoA), which fuels various metabolic pathways and is also the acyl donor for protein lysine acetylation. Notably, histone acetylation is sensitive to acetyl-CoA availability and nutrient replete conditions induce a substantial accumulation of acetylation on histones. Deacetylation releases acetate, which can be recycled to acetyl-CoA, suggesting that deacetylation could be mobilized as an acetyl-CoA source to feed downstream metabolic processes under nutrient depletion. While the notion of histones as a metabolic reservoir has been frequently proposed, experimental evidence has been lacking. Therefore, to test this concept directly, we developed an experimental system to trace deacetylation-derived acetate and its incorporation into acetyl-CoA, using 13C2-acetate in ATP citrate lyase-deficient fibroblasts (Acly-/- MEFs), which are primarily dependent on acetate for protein acetylation. We find that dynamic protein deacetylation in Acly-/- MEFs contributes carbons to acetyl-CoA and proximal downstream metabolites. However, there is no significant effect on acyl-CoA pool sizes, and even at maximal acetylation, deacetylation transiently supplies approximately 9% of cellular acetyl-CoA. Together, our data reveal that although protein acetylation is dynamic and sensitive to nutrient availability, its potential for maintaining cellular acetyl-CoA-dependent metabolic pathways is limited compared to cellular demand.

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Soaita, I., Megill, E., Kantner, D., Chatoff, A., Arany, Z., Snyder, N. W., Wellen, K. E., Trefely, S. W.. 2022-12-29. Dynamic protein deacetylation is a limited carbon source for acetyl-CoA-dependent metabolism. https://doi.org/10.1101/2022.12.28.522149

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