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AAA+ ATPase chaperone p97/VCPFAF2 governs basal pexophagy
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AAA+ ATPase chaperone p97/VCPFAF2 governs basal pexophagy
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AAA+ ATPase chaperone p97/VCPFAF2 governs basal pexophagy
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Journal Article
AAA+ ATPase chaperone p97/VCPFAF2 governs basal pexophagy
2024
Overview
Peroxisomes are organelles that are central to lipid metabolism and chemical detoxification. Despite advances in our understanding of peroxisome biogenesis, the mechanisms maintaining peroxisomal membrane proteins remain to be fully elucidated. We show here that mammalian FAF2/UBXD8, a membrane-associated cofactor of p97/VCP, maintains peroxisomal homeostasis by modulating the turnover of peroxisomal membrane proteins such as PMP70. In FAF2-deficient cells, PMP70 accumulation recruits the autophagy adaptor OPTN (Optineurin) to peroxisomes and promotes their autophagic clearance (pexophagy). Pexophagy is also induced by p97/VCP inhibition. FAF2 functions together with p97/VCP to negatively regulate pexophagy rather than as a factor for peroxisome biogenesis. Our results strongly suggest that p97/VCP
FAF2
-mediated extraction of ubiquitylated peroxisomal membrane proteins (e.g., PMP70) prevents peroxisomes from inducing nonessential autophagy under steady state conditions. These findings provide insight into molecular mechanisms underlying the regulation of peroxisomal integrity by p97/VCP and its associated cofactors.
The mechanisms maintaining peroxisomal membrane proteins remain to be fully elucidated. Here, the authors report that p97/VCP and FAF2/UBXD8 modulate the turnover of peroxisomal membrane proteins to prevent autophagic degradation of peroxisomes.
