Evidence map›Paper›PMID 30700497›Full record

ArticleThe Journal of cell biology2019

Deubiquitinating enzyme USP30 maintains basal peroxisome abundance by regulating pexophagy.

Victoria Riccio, Nicholas Demers, Rong Hua, Miluska Vissa, Derrick T Cheng, Amy Wong Strilchuk, Yuqing Wang, G Angus McQuibban, Peter Kijun Kim

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 2 pooled it
7.0field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 2 syntheses or guidelines pooled it, 74 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. AAA+ ATPase chaperone p97/VCPNature communications · 2024
    Article
  12. Review
  13. Article
  14. Mammalian pexophagy at a glance.Journal of cell science · 2024
    Review
  15. Article
  16. Article
  17. Fluorescence Methods to Measure Pexophagy.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Victoria RiccioBiochemistry Department, University of Toronto, Canada.ORCID 0000-0001-6111-4085
Nicholas DemersBiochemistry Department, University of Toronto, Canada.
Rong HuaCell Biology Department, Hospital for Sick Children, Toronto, Canada.
Miluska VissaCell Biology Department, Hospital for Sick Children, Toronto, Canada.
Derrick T ChengBiochemistry Department, University of Toronto, Canada.
Amy Wong StrilchukBiochemistry Department, University of Toronto, Canada.
Yuqing WangBiochemistry Department, University of Toronto, Canada.
G Angus McQuibbanBiochemistry Department, University of Toronto, Canada angus.mcquibban@utoronto.ca.
Peter Kijun KimBiochemistry Department, University of Toronto, Canada pkim@sickkids.ca.ORCID 0000-0001-6626-0575
University of Toronto · CAHospital for Sick Children · CA

Funding

CIHR MOP-130281CIHR PJT156196
6 · The paper itself

Abstract

The regulation of organelle abundance is critical for cell function and survival; however, the mechanisms responsible are not fully understood. In this study, we characterize a role of the deubiquitinating enzyme USP30 in peroxisome maintenance. Peroxisomes are highly dynamic, changing in abundance in response to metabolic stress. In our recent study identifying the role of USP30 in mitophagy, we observed USP30 to be localized to punctate structures resembling peroxisomes. We report here that USP30, best known as a mitophagy regulator, is also necessary for regulating pexophagy, the selective autophagic degradation of peroxisomes. We find that overexpressing USP30 prevents pexophagy during amino acid starvation, and its depletion results in pexophagy induction under basal conditions. We demonstrate that USP30 prevents pexophagy by counteracting the action of the peroxisomal E3 ubiquitin ligase PEX2. Finally, we show that USP30 can rescue the peroxisome loss observed in some disease-causing peroxisome mutations, pointing to a potential therapeutic target.

Indexed as

MitophagyStress, PhysiologicalAnimalsChlorocebus aethiopsCOS CellsHeLa CellsHumansMiceMitochondrial ProteinsMutationPeroxisomal Biogenesis Factor 2PeroxisomesThiolester HydrolasesMitochondrial ProteinsPeroxisomal Biogenesis Factor 2PEX2 protein, humanPEX2 protein, mouseThiolester HydrolasesUsp30 protein, human

Identifiers

PMID30700497
PMCPMC6400567
OpenAlexW2911686738

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.