unconventional protein secretion
traitmech:000648 · CLASS · PROPOSED
A physiological phenotype in which a eukaryotic microbial cell delivers protein cargo to the plasma membrane or extracellular space by a route that bypasses part or all of the conventional endoplasmic-reticulum-Golgi-plasma-membrane secretory itinerary.
Trait evidence
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DOI:10.3389/fcell.2022.852028Our results show that neosynthesized PmaA and PalI are translocated to the PM via Golgi-bypass, similar to nutrient transporters.
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DOI:10.7554/eLife.16299Under these conditions Acb1, but not Cof1, was detected in the cell wall extract of starving cells
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DOI:10.1083/jcb.201407119Altogether our findings indicate that CUPS are not specialized autophagosomes as suggested previously.
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DOI:10.1083/jcb.202312120Notably, while CUPS remain stable, the modified TGN undergoes remodeling during the later stages of unconventional secretion.
Provenance
- Identifier source
- TraitMech local identifier
- Definition source
DOI:10.3389/fcell.2022.852028
Parent traits (1)
kg-microbe context
No kg-microbe node embedding matched this record in the 2026-04-25 deepwalk.
Discussions and Knowledge Gaps
Keep cargo destinations and route-specific meanings distinct.
The broad usage in DOI:10.3389/fcell.2022.852028 includes plasma-membrane delivery after ER entry; DOI:10.7554/eLife.16299 describes an ER-bypassing soluble-cargo route. Preserve both, rather than treating leaderless secretion, Golgi bypass or secretory autophagy as exact synonyms. This concerns traffic performed by a eukaryotic microbe, not its animal or plant host. An absent predicted signal peptide, ATG dependence, CUPS formation or protein detected after lysis alone is insufficient. Membrane localization does not establish soluble release. The degradative autophagy record traitmech:000638 is not a broader parent; exocytosis traitmech:000637 specifies fusion-pore release rather than an unconventional itinerary. Overlap is not disjointness. Obsolete METPO secretion classes do not supply an active exact term. Keep METPO:1000059 as parent and leave ontology equivalences and finer route hierarchy for human review.
Resolve natural exemplars and mechanisms separately for each route.
Retain qualified laboratory observations without labeling engineered fluorescent cargo or conditional trafficking mutants as natural canonical exemplars. Natural strain provenance, source figures and accession-level functional evidence need further review before adding examples or a protein-resolved graph. The three CUPS papers share investigators and are not independent-laboratory replications; the Aspergillus study supports a different route, not replication of CUPS. No universal starvation trigger, signal-peptide absence, COPII independence, autophagosome or conserved export apparatus is asserted. ATG-dependent export remains a possible narrower research target, not an allocated additional trait.
Curation history
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MINTED_TRAITMECH_ID · codex
Added unconventional protein secretion with four DOI-backed snippets and explicit soluble-export, membrane-delivery, route and assay limits. Ignored-and-hidden searches and pinned METPO review found no exact record. Reserved METPO:1060100 in v524. Deferred unverified mappings, natural exemplars and protein mechanisms; existing records remain unchanged.
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CURATED_WITH_LITERATURE · codex
Clarified the conventional itinerary through plasma-membrane delivery (#1760), preserving the definition source's inclusion of unconventional post-Golgi export. No new route, cargo, taxon or universal mechanism is inferred.