Abstract
Peroxisomes are organelles with key roles in metabolism including long-chain fatty acid production. Their metabolic functions overlap and interconnect with mitochondria, with which they share an overlapping but distinct proteome. Both organelles are degraded by selective autophagy processes termed pexophagy and mitophagy. Whilst mitophagy has received intense attention, the pathways linked to pexophagy and associated tools are less well developed. We have identified the neddylation inhibitor, MLN4924, as a potent activator of pexophagy and show that this is mediated by the HIF1α-dependent upregulation of BNIP3L/NIX, a known adaptor for mitophagy. We show that this pathway is distinct from pexophagy induced by the USP30 deubiquitylase inhibitor, CMPD-39, for which we identify the adaptor NBR1 as a central player. Our work suggests a level of complexity to the regulation of peroxisome turnover that includes the capacity to co-ordinate with mitophagy, via NIX, which acts as a rheostat for both processes.
Competing Interest Statement
The authors have declared no competing interest.
Footnotes
Email urbe{at}liv.ac.uk
