The PARK10 gene USP24 is a negative regulator of autophagy and ULK1 protein stability.

ABSTRACT

Recent studies indicate a causative relationship between defects in autophagy and dopaminergic neuron degeneration in Parkinson disease (PD). However, it is not fully understood how autophagy is regulated in the context of PD. Here we identify USP24 (ubiquitin specific peptidase 24), a gene located in the PARK10 (Parkinson disease 10 [susceptibility]) locus associated with late onset PD, as a novel negative regulator of autophagy. Our data indicate that USP24 regulates autophagy by affecting ubiquitination and stability of the ULK1 protein. Knockdown of USP24 in cell lines and in human induced-pluripotent stem cells (iPSC) differentiated into dopaminergic neurons resulted in elevated ULK1 protein levels and increased autophagy flux in a manner independent of MTORC1 but dependent on the class III phosphatidylinositol 3-kinase (PtdIns3K) activity. Surprisingly, USP24 knockdown also improved neurite extension and/or maintenance in aged iPSC-derived dopaminergic neurons. Furthermore, we observed elevated levels of USP24 in the substantia nigra of a subpopulation of idiopathic PD patients, suggesting that USP24 may negatively regulate autophagy in PD.Abbreviations Bafilomycin/BafA bafilomycin A1; DUB deubiquitinating enzyme; iPSC induced pluripotent stem cells; MTOR mechanistic target of rapamycin kinase; MTORC1 MTOR complex 1; nt non-targeting; PD Parkinson disease; p-ATG13 phospho-ATG13; PtdIns3P phosphatidylinositol 3-phosphate; RPS6 ribosomal protein S6; SNPs single nucleotide polymorphisms; TH tyrosine hydroxylase; USP24 ubiquitin specific peptidase 24.