nucleophagy
traitmech:000643 · CLASS · PROPOSED
An autophagy phenotype in which a microbial cell degrades parts of its nucleus or an entire nucleus by delivering nuclear material to lysosomal or vacuolar compartments.
Trait evidence
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DOI:10.1091/mbc.e02-08-0483During PMN, teardrop-like blebs are pinched from the nucleus, released into the vacuole lumen, and degraded by soluble hydrolases.
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DOI:10.1091/mbc.e08-04-0363We conclude that a spectrum of ATG genes is required for the terminal vacuole enclosure and fusion stages of PMN.
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DOI:10.1007/s00284-024-03838-yThese results indicate that nuclei are engulfed in the autophagosomes as a whole and transported/released into the vacuolar lumen where they are degraded.
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DOI:10.1371/journal.pone.0033270infection-associated nuclear degeneration in M. oryzae instead occurs by non-selective macroautophagy, which is necessary for rice blast disease.
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DOI:10.1242/jcs.133090A selective form of autophagy, known as nucleophagy, can be used to accomplish the degradation of nucleus-derived material.
Provenance
- Identifier source
- TraitMech local identifier
- Definition source
DOI:10.1007/s00284-024-03838-y
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 nuclear-cargo scope and source-specific selectivity.
Include nuclear portions and entire nuclei, micro and macro routes. The 2013 review defines nucleophagy as selective, whereas the 2024 Discussion includes the 2012 nonselective Magnaporthe route. The present cargo-defined phenotype does not require universal selectivity; preserve this attributed difference for human review. GO:0044804, resolved at https://www.ebi.ac.uk/QuickGO/services/ontology/go/terms/GO%3A0044804, is nonobsolete and includes nuclear parts or entire nuclei without an explicit selectivity restriction. Its biological process scope is not an exact organismal-phenotype xref. The autophagy parent traitmech:000638 is corrected to intracellular cargo in this change (#1754). Nuclear-envelope overlap with ER-phagy traitmech:000642 does not make the records equivalent. No exact synonyms or SSSOM mapping are asserted. Nuclear damage, loss of fluorescence or DNA degradation alone does not prove autophagic delivery and flux.
Resolve native exemplars and route-specific mechanisms.
The microbial cell carrying out degradation has the phenotype, not a bacterium eliciting an animal-host response. Whole-nucleus turnover in multinucleate cells need not cause cell death. Do not equate blebs, puncta, inhibited autophagic bodies, gene presence or partial rate reductions with completed flux or total absence. The 2003/2008 PMN dependence conflict needs full-text assay reconciliation before protein-resolved causal claims. Canonical examples remain unset pending independent natural-strain provenance; do not infer origin from a mutant label. Native taxon-paired protein accessions and functional evidence are required before adding a causal graph.
Curation history
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MINTED_TRAITMECH_ID · codex
Added nuclear-cargo autophagy with five DOI-backed snippets, source-attributed selectivity and flux limits. Corrected its autophagy parent's cytoplasmic-only wording (#1754). Ignored-and-hidden novelty checks found no exact record; reserved METPO:1059600 in v519. Deferred unverified exemplars, mappings and protein graphs.