Version 1
: Received: 25 October 2024 / Approved: 28 October 2024 / Online: 28 October 2024 (14:26:54 CET)
How to cite:
Zhang, Y.; Zhang, B. B.; Bharathi, S. S.; Bons, J.; Rose, J. P.; Shah, S.; Dobrowolski, S. F.; Sims-Lucas, S.; Schilling, B.; Goetzman, E. S. Sirtuin‐5 Is Recruited to Hepatic Peroxisomes in Mice Fed Dodecanedioic Acid but Has Little Impact on the Peroxisomal Succinylome. Preprints2024, 2024102196. https://doi.org/10.20944/preprints202410.2196.v1
Zhang, Y.; Zhang, B. B.; Bharathi, S. S.; Bons, J.; Rose, J. P.; Shah, S.; Dobrowolski, S. F.; Sims-Lucas, S.; Schilling, B.; Goetzman, E. S. Sirtuin‐5 Is Recruited to Hepatic Peroxisomes in Mice Fed Dodecanedioic Acid but Has Little Impact on the Peroxisomal Succinylome. Preprints 2024, 2024102196. https://doi.org/10.20944/preprints202410.2196.v1
Zhang, Y.; Zhang, B. B.; Bharathi, S. S.; Bons, J.; Rose, J. P.; Shah, S.; Dobrowolski, S. F.; Sims-Lucas, S.; Schilling, B.; Goetzman, E. S. Sirtuin‐5 Is Recruited to Hepatic Peroxisomes in Mice Fed Dodecanedioic Acid but Has Little Impact on the Peroxisomal Succinylome. Preprints2024, 2024102196. https://doi.org/10.20944/preprints202410.2196.v1
APA Style
Zhang, Y., Zhang, B. B., Bharathi, S. S., Bons, J., Rose, J. P., Shah, S., Dobrowolski, S. F., Sims-Lucas, S., Schilling, B., & Goetzman, E. S. (2024). Sirtuin‐5 Is Recruited to Hepatic Peroxisomes in Mice Fed Dodecanedioic Acid but Has Little Impact on the Peroxisomal Succinylome. Preprints. https://doi.org/10.20944/preprints202410.2196.v1
Chicago/Turabian Style
Zhang, Y., Birgit Schilling and Eric S. Goetzman. 2024 "Sirtuin‐5 Is Recruited to Hepatic Peroxisomes in Mice Fed Dodecanedioic Acid but Has Little Impact on the Peroxisomal Succinylome" Preprints. https://doi.org/10.20944/preprints202410.2196.v1
Abstract
Lysine succinylation, and its reversal by sirtuin-5 (SIRT5), is known to modulate mitochondrial fatty acid β-oxidation (FAO). We recently showed that feeding mice dodecanedioic acid, a 12-carbon dicarboxylic acid (DC12) that can be chain-shortened four rounds to succinyl-CoA, drives high-level protein hypersuccinylation in the peroxisome, particularly on peroxisomal FAO enzymes. But the ability of SIRT5 to reverse DC12-induced peroxisomal succinylation, or to regulate peroxisomal FAO in this context, remained unexplored. Here, we showed that feeding DC12 strongly recruits SIRT5 into hepatic peroxisomes. Knocking out SIRT5 impaired peroxisomal FAO as evidenced by reduced 14C-DC12 flux in liver homogenates and elevated levels of partially shortened DC12 catabolites in urine. Further, mass spectrometry revealed a trend toward less peroxisomal protein succinylation in SIRT5 knockout liver. This is consistent with reduced flux of DC12 through the peroxisomal FAO pathway, thereby reducing production of the succinyl-CoA that chemically reacts with lysine residues to produce protein succinylation. Mass spectrometry comparisons of site-level succinylation in wildtype and SIRT5 knockout liver did not reveal any clear pattern of SIRT5 target sites in the peroxisome after DC12 feeding. However, SIRT5 co-immunoprecipitated with 15 peroxisomal proteins including the key peroxisomal FAO enzymes acyl-CoA oxidase-1 and enoyl-CoA/3-hydroxyacyl-CoA dehydrogenase (EHHADH). In vitro, recombinant SIRT5 partially desuccinylated chemically modified recombinant ACOX1a, ACOX1b, and EHHADH. Desuccinylation by SIRT5 had no effect on enzyme activity for ACOX1a and EHHADH. For ACOX1b, SIRT5-mediated desuccinylation decreased activity by ~15%. Possible interpretations of this data are discussed.
Keywords
peroxisome; sirtuin-5; fatty acid oxidation
Subject
Biology and Life Sciences, Endocrinology and Metabolism
Copyright:
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
