pexophagy
traitmech:000640 · CLASS · PROPOSED
An autophagy phenotype in which a microbial cell selectively degrades its peroxisomes by delivering them to lysosomal or vacuolar compartments.
Trait evidence
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DOI:10.1038/emboj.2012.151Peroxisomes undergo rapid, selective autophagic degradation (pexophagy) when the metabolic pathways they contain are no longer required for cellular metabolism.
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DOI:10.1016/j.devcel.2007.12.011It is necessary for pexophagy, but not for other selective and nonselective autophagy-related processes.
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DOI:10.1242/jcs.108.1.25there exist in P. pastoris at least two pathways for the sequestration of peroxisomes into the vacuole for degradation.
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DOI:10.1080/15548627.2019.1603546the cytosolic pools of PTS receptors and their cargoes are degraded via a pexophagy-independent, selective autophagy pathway under pexophagy conditions.
Provenance
- Identifier source
- TraitMech local identifier
- Definition source
DOI:10.1038/emboj.2012.151
Parent traits (1)
kg-microbe context
No kg-microbe node embedding matched this record in the 2026-04-25 deepwalk.
Discussions and Knowledge Gaps
Review route-inclusive phenotype against narrower GO terminology.
Use autophagy traitmech:000638 as the direct broader phenotype. The 2008 PpAtg30 scientific abstract uses pexophagy for both micropexophagy and macropexophagy. In contrast, issuing GO:0000425 names pexophagy specifically for selective macroautophagy and lists macropexophagy as exact; GO:0000426 micropexophagy is its sibling under GO:0030242 autophagy of peroxisome, which lists pexophagy as related. These nonobsolete biological-process records were resolved at https://www.ebi.ac.uk/QuickGO/services/ontology/go/terms/GO%3A0000425,GO%3A0000426,GO%3A0030242. Retain the source-attributed route-inclusive interpretation for human review and omit exact phenotype xrefs and synonyms. Bulk incidental capture, peroxisome presence, import defects, puncta, protein abundance and delivery without degradation alone are insufficient. Cytosolic peroxisomal-protein autophagy is a separate endpoint. The microbial cell doing the degradation carries the trait, not an organism merely inducing an animal host response.
Resolve strain provenance and taxon-paired mechanisms before expansion.
The evidence uses reporter and perturbation strains; natural strain provenance is not independently established. Keep canonical examples unset rather than presenting deficient mutants as positive exemplars. Historical Pichia names also need strain-specific taxonomic review. Atg36 in budding yeast and PpAtg30 do not define a universal receptor inventory; putative BLAST orthologues are not functional protein examples. Require native taxon-paired protein accession checks and direct functional evidence before a causal graph. Neither an ATG locus nor a detector profile is the phenotype, and neither starvation nor damaged cargo is universally required.
Curation history
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MINTED_TRAITMECH_ID · codex
Added pexophagy as selective peroxisome degradation under autophagy, with four DOI-backed snippets and explicit route, flux and cytosolic-protein boundaries. Ignored-and-hidden searches and pinned METPO review found no exact record. Reserved METPO:1059300 in v516, carrying v514's unchanged parent row as context. Deferred unverified examples, mappings and protein graphs.