Journal Article

SIRT4 positively regulates autophagy via ULK1, but independently of HDAC6 and OPA1

Nguyen, Jasmin Thuy Vy, Gabriel, Lydia, Stork, Björn, Hesse, Julia, Floss, Doreen M., Amin, Khawar, Lehmkuhl, Isabell, Hampel, Nils, Wiek, Constanze, Hanenberg, Helmut, Ahmadian, M. Reza, Piekorz, Roland P., Iram, Afshin, Scheller, Jürgen

2026

Overview

The sirtuin SIRT4 has been implicated in the control of autophagy and mitochondrial quality control via mitophagy. However, the role of SIRT4 in regulating autophagy/mitophagy induced by different stressors is unclear. Here, we show that cells expressing SIRT4(H161Y), a catalytically inactive, dominant‐negative mutant of SIRT4, fail to upregulate LC3B‐II. These cells also exhibit a reduced autophagic flux upon treatment with different inducers of mitophagy/autophagy, that is, CoCl2‐triggered pseudohypoxia, CCCP (carbonyl cyanide 3‐chlorophenylhydrazone)/oligomycin‐mediated respiratory chain inhibition, or rapamycin treatment. Interestingly, SIRT4(H161Y) expression upregulated protein levels of HDAC6, which is involved in mitochondrial trafficking and autophagosome‐lysosome fusion, and inhibited the conversion of OPA1‐L to OPA1‐S, which is associated with increased mitochondrial fusion and decreased mitophagy. Both HDAC6 and OPA1 are SIRT4 interactors. However, the pharmacological inhibition of HDAC6 using Tubacin or of OPA1 using MYLS22 did not restore the stress‐induced upregulation of LC3B‐II levels upon autophagy/mitophagy treatment in SIRT4(H161Y)‐expressing cells. Remarkably, inhibition of autophagosome–lysosome fusion and thus disruption of late autophagic flux by BafA1 treatment also failed to restore LC3B‐II levels upon autophagy/mitophagy treatment, suggesting an inhibitory effect of SIRT4(H161Y) on the initiation/early phase of autophagy. Consistent with this, we demonstrate that SIRT4(H161Y) promotes the phosphorylation of ULK1 at S638 and S758 (mTORC1 targets), both of which mediate an important inhibitory regulation of autophagy initiation. Thus, our data suggest a positive regulatory function of SIRT4 in the ULK1‐dependent early regulation/initiation of stress‐induced autophagic flux, presumably via modulation of AMPK/mTORC1 signaling. Cells expressing SIRT4 (H161Y), a catalytically inactive mutant of the sirtuin SIRT4, fail to upregulate LC3B‐II and exhibit a reduced autophagic flux under stress conditions. Interestingly, SIRT4(H161Y) promotes phosphorylation of ULK1 at S638 and S758 that are associated with inhibition of autophagy initiation. Thus, SIRT4 may function in ULK1‐dependent early regulation/initiation of autophagic flux, presumably via modulation of AMPK/mTORC1 signaling.

• Publisher: John Wiley & Sons, Inc,Wiley
• Subject: Autophagy / Autophagy - physiology / Autophagy-Related Protein-1 Homolog - metabolism / Electron transport / GTP Phosphohydrolases - metabolism / HDAC6 / Histone Deacetylase 6 - metabolism / Humans / Intracellular Signaling Peptides and Proteins / LC3 / Mitochondria / Mitochondria - metabolism / Mitochondrial Proteins / Mitophagy / Oligomycin / OPA1 / Phosphorylation / Protein transport / Quality control / Rapamycin / SIRT4 / Sirtuins - genetics / Sirtuins - metabolism / ULK1