Evidence map›Paper›PMID 21427232›Full record

ArticleMolecular & cellular proteomics : MCP2011

A perturbed ubiquitin landscape distinguishes between ubiquitin in trafficking and in proteolysis.

Inbal Ziv, Yulia Matiuhin, Donald S Kirkpatrick, Zoi Erpapazoglou, Sebastien Leon, Marina Pantazopoulou, Woong Kim, Steven P Gygi, Rosine Haguenauer-Tsapis, Noa Reis and 2 more

Abstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
–field-weighted citation impact
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

82 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. The Molecular Toolbox for Linkage Type-Specific Analysis of Ubiquitin Signaling.Chembiochem : a European journal of chemical biology · 2025
    Review
  5. Light-Activatable Ubiquitin for Studying Linkage-Specific Ubiquitin Chain Formation Kinetics.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Ubiquitination and Metabolic Disease.Advances in experimental medicine and biology · 2024
    Review
  11. Article
  12. The Ubiquitin-like Proteins ofBiomolecules · 2023
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Insights in Post-Translational Modifications: Ubiquitin and SUMO.International journal of molecular sciences · 2022
    Review
  18. Emerging Roles of Non-proteolytic Ubiquitination in Tumorigenesis.Frontiers in cell and developmental biology · 2022
    Review
  19. Review
  20. Structural Diversity of Ubiquitin E3 Ligase.Molecules (Basel, Switzerland) · 2021
    Review

22 more citing papers are in PubMed but not listed here.

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

12 authors.

Inbal ZivDepartment of Biology, Technion Israel institute of Technology, Haifa 32000, Israel.
Yulia Matiuhin
Donald S Kirkpatrick
Zoi Erpapazoglou
Sebastien Leon
Marina Pantazopoulou
Woong Kim
Steven P Gygi
Rosine Haguenauer-Tsapis
Noa Reis
Michael H Glickman
Oded Kleifeld

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Any of seven lysine residues on ubiquitin can serve as the base for chain-extension, resulting in a sizeable spectrum of ubiquitin modifications differing in chain length or linkage type. By optimizing a procedure for rapid lysis, we charted the profile of conjugated cellular ubiquitin directly from whole cell extract. Roughly half of conjugated ubiquitin (even at high molecular weights) was nonextended, consisting of monoubiquitin modifications and chain terminators (endcaps). Of extended ubiquitin, the primary linkages were via Lys48 and Lys63. All other linkages were detected, contributing a relatively small portion that increased at lower molecular weights. In vivo expression of lysineless ubiquitin (K0 Ub) perturbed the ubiquitin landscape leading to elevated levels of conjugated ubiquitin, with a higher mono-to-poly ratio. Affinity purification of these trapped conjugates identified a comprehensive list of close to 900 proteins including novel targets. Many of the proteins enriched by K0 ubiquitination were membrane-associated, or involved in cellular trafficking. Prime among them are components of the ESCRT machinery and adaptors of the Rsp5 E3 ubiquitin ligase. Ubiquitin chains associated with these substrates were enriched for Lys63 linkages over Lys48, indicating that K0 Ub is unevenly distributed throughout the ubiquitinome. Biological assays validated the interference of K0 Ub with protein trafficking and MVB sorting, minimally affecting Lys48-dependent turnover of proteasome substrates. We conclude that despite the shared use of the ubiquitin molecule, the two branches of the ubiquitin machinery--the ubiquitin-proteasome system and the ubiquitin trafficking system--were unevenly perturbed by expression of K0 ubiquitin.

Indexed as

LysineMutant ProteinsMutation, MissenseProteasome Endopeptidase ComplexProtein TransportProteomeSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsUbiquitinUbiquitinated ProteinsUbiquitinationLysineMutant ProteinsProteasome Endopeptidase ComplexProteomeSaccharomyces cerevisiae ProteinsUbiquitinUbiquitinated Proteins

Identifiers

PMID21427232
PMCPMC3098606

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Registered trials

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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.