Evidence map›Paper›PMID 35159231›Full record

ReviewCells2022

Functional Differences between Proteasome Subtypes.

Joanna Abi Habib, Julie Lesenfants, Nathalie Vigneron, Benoit J Van den Eynde

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
6.0field-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

50 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Oligomerization of PER2 as a dynamic mode of regulation of the mammalian circadian clock.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  10. Role of E5 from HPV16 in the Evasion of the Immune Response.International journal of molecular sciences · 2026
    Review
  11. Review
  12. PSMB8 stratifies therapy response in eosinophilic esophagitis.Clinical and experimental immunology · 2026
    Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Ubiquitin-proteasome system in the different stages of dominantly inherited Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  19. The Role of the Ubiquitin System in Eye Diseases.Life (Basel, Switzerland) · 2025
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 4 institutions in 2 countries.

Joanna Abi HabibLudwig Institute for Cancer Research, 1200 Brussels, Belgium.
Julie LesenfantsLudwig Institute for Cancer Research, 1200 Brussels, Belgium.
Nathalie VigneronLudwig Institute for Cancer Research, 1200 Brussels, Belgium.
Benoit J Van den EyndeLudwig Institute for Cancer Research, 1200 Brussels, Belgium.
de Duve Institute · BELudwig Cancer Research · BEUniversity of Oxford · GBWalloon Excellence in Lifesciences and Biotechnology · BE

Funding

Fonds National de la Recherche Scientifique (F.N.R.S.) PDR T.0091.18Fonds National de la Recherche Scientifique (F.N.R.S), Fonds Wetenschappelijk Onderzoek- Vlaanderen (F.W.O) EOS: 30837538Fonds National de la Recherche Scientifique (F.N.R.S.-Télévie) 7650819F
6 · The paper itself

Abstract

Four proteasome subtypes are commonly present in mammalian tissues: standard proteasomes, which contain the standard catalytic subunits β1, β2 and β5; immunoproteasomes containing the immuno-subunits β1i, β2i and β5i; and two intermediate proteasomes, containing a mix of standard and immuno-subunits. Recent studies revealed the expression of two tissue-specific proteasome subtypes in cortical thymic epithelial cells and in testes: thymoproteasomes and spermatoproteasomes. In this review, we describe the mechanisms that enable the ATP- and ubiquitin-dependent as well as the ATP- and ubiquitin-independent degradation of proteins by the proteasome. We focus on understanding the role of the different proteasome subtypes in maintaining protein homeostasis in normal physiological conditions through the ATP- and ubiquitin-dependent degradation of proteins. Additionally, we discuss the role of each proteasome subtype in the ATP- and ubiquitin-independent degradation of disordered proteins. We also discuss the role of the proteasome in the generation of peptides presented by MHC class I molecules and the implication of having different proteasome subtypes for the peptide repertoire presented at the cell surface. Finally, we discuss the role of the immunoproteasome in immune cells and its modulation as a potential therapy for autoimmune diseases.

Indexed as

Proteasome Endopeptidase ComplexUbiquitinAdenosine TriphosphateAnimalsCytoplasmHistocompatibility Antigens Class IMammalsPeptidesAdenosine TriphosphateHistocompatibility Antigens Class IPeptidesProteasome Endopeptidase ComplexUbiquitinATP- and ubiquitin-dependent degradationATP- and ubiquitin-independent degradationautoimmune diseasesMHC class I peptidesproteasome subtypesprotein degradation

Identifiers

PMID35159231
PMCPMC8834425
OpenAlexW4210413648

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.