ribophagy
traitmech:000641 · CLASS · PROPOSED
An autophagy phenotype in which a microbial cell selectively degrades mature ribosomes or their subunits through macroautophagic delivery to lysosomal or vacuolar compartments.
Trait evidence
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DOI:10.1038/ncb1723A genetic screen revealed that selective degradation of ribosomes requires catalytic activity of the Ubp3p/Bre5p ubiquitin protease.
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DOI:10.1083/jcb.201308139Its ubiquitylation is Ltn1 dependent and Ubp3 reversed, and mutation of its ubiquitylation site rendered ribophagy less dependent on Ubp3.
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DOI:10.15252/embj.201489083Under nutrient starvation, a portion of the cytoplasm is non-selectively sequestered into autophagosomes.
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DOI:10.1016/j.jbc.2025.108554We discovered that most ribosomes are selectively degraded, whose mechanism differs from the previously reported selective degradation process called "ribophagy."
Provenance
- Identifier source
- TraitMech local identifier
- Definition source
DOI:10.1038/ncb1723
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 cargo selectivity and mechanism-dependent terminology.
Use autophagy traitmech:000638 as the broader phenotype. The 2008 paper names selective mature-ribosome turnover ribophagy; the 2014 paper explicitly includes 60S subunits. Neither ribosome protection in dormancy nor bulk RNA decay, free ribosomal-protein degradation, ribosome biogenesis, gene presence or puncta alone establishes this phenotype. The 2025 Rsa1 paper distinguishes its pathway from known ribophagy and notes differing mammalian usage. Retain that source-attributed distinction for human review; do not silently equate Rsa1-dependent turnover with the historically named pathway or make Ubp3 universal. GO:0034517, resolved at https://www.ebi.ac.uk/QuickGO/services/ontology/go/terms/GO%3A0034517, is a nonobsolete biological process for selective mature ribosome degradation by macroautophagy, not an exact organismal phenotype. Preserve that route qualifier and omit exact xrefs and synonyms.
Resolve natural exemplars and subunit-specific mechanisms.
Canonical examples remain unset: the experiments use laboratory reporter and perturbation strains, and natural strain provenance has not been independently verified. The microbial cell doing the degradation carries the phenotype, not bacteria expressing purified yeast proteins or organisms eliciting an animal host response. Require native taxon-paired protein accessions and functional evidence before a causal graph; do not impose the 60S Ubp3/Bre5 mechanism on 40S turnover or all microbial taxa. Preserve the difference between normal rates, residual activity and complete absence of degradation. A predicted binding motif is not a separate trait or a proven causal contact.
Curation history
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MINTED_TRAITMECH_ID · codex
Added ribophagy as selective mature ribosome or subunit degradation under autophagy, with four DOI-backed snippets and explicit bulk-turnover, source-access and terminology limits. Ignored-and-hidden searches and pinned METPO review found no exact record. Reserved METPO:1059400 in v517 with v514's unchanged parent context. Deferred unverified examples, mappings and protein graphs.