KAT8 compound inhibition inhibits the initial steps of PINK1-dependant mitophagy

• Published in: Scientific reports 2024-05, Vol.14 (1), p.11721-11721, Article 11721
• Main Authors: de Talhouët, Capucine, Esteras, Noemi, Soutar, Marc P. M., O’Callaghan, Benjamin, Plun-Favreau, Helene
• Format: Article
• Language: English
• Subjects: 631/80/304; 631/80/39; 631/80/39/2348; Acetyltransferase; Autophagy; Epigenetics; Genome-wide association studies; Genomes; HeLa Cells; Histone Acetyltransferases - antagonists & inhibitors; Histone Acetyltransferases - metabolism; Humanities and Social Sciences; Humans; KAT8; Lysosomes; Membrane Potential, Mitochondrial - drug effects; MG149; Mitochondria; Mitochondria - drug effects; Mitochondria - metabolism; Mitophagy; Mitophagy - drug effects; multidisciplinary; Neurodegenerative diseases; Parkin protein; Parkinson's disease; Phosphorylation; Phosphorylation - drug effects; Protein Kinases - genetics; Protein Kinases - metabolism; PTEN-induced putative kinase; Science; Science (multidisciplinary); Toxins; Ubiquitin; Ubiquitin-Protein Ligases - genetics; Ubiquitin-Protein Ligases - metabolism
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-60602-9

It has recently been shown that KAT8 , a genome-wide association study candidate risk gene for Parkinson’s Disease, is involved in PINK1/Parkin-dependant mitophagy. The KAT8 gene encodes a lysine acetyltransferase and represents the catalytically active subunit of the non-specific lethal epigenetic remodelling complex. In the current study, we show that contrary to KAT5 inhibition, dual inhibition of KAT5 and KAT8 via the MG149 compound inhibits the initial steps of the PINK1-dependant mitophagy process. More specifically, our study shows that following mitochondrial depolarisation induced by mitochondrial toxins, MG149 treatment inhibits PINK1-dependant mitophagy initiation by impairing PINK1 activation, and subsequent phosphorylation of Parkin and ubiquitin. While this inhibitory effect of MG149 on PINK1-activation is potent, MG149 treatment in the absence of mitochondrial toxins is sufficient to depolarise the mitochondrial membrane, recruit PINK1 and promote partial downstream recruitment of the autophagy receptor p62, leading to an increase in mitochondrial delivery to the lysosomes. Altogether, our study provides additional support for KAT8 as a regulator of mitophagy and autophagy processes.