Evidence map›Paper›PMID 26917723›Full record

ArticleThe Journal of biological chemistry2016

USP5 Is Dispensable for Monoubiquitin Maintenance in Drosophila.

Gorica Ristic, Wei-Ling Tsou, Ermal Guzi, Adam J Kanack, Kenneth Matthew Scaglione, Sokol V Todi

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Unanchored Ubiquitin Chains, Revisited.Frontiers in cell and developmental biology · 2020
    Review
  5. Article
  6. Article
  7. Article
  8. 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

6 authors at 2 institutions in 1 country.

Gorica RisticFrom the Departments of Pharmacology and.
Wei-Ling TsouFrom the Departments of Pharmacology and.
Ermal GuziFrom the Departments of Pharmacology and.
Adam J Kanackthe Department of Biochemistry and the Neuroscience Research Center, Medical College of Wisconsin, Milwaukee Wisconsin 53226.
Kenneth Matthew Scaglionethe Department of Biochemistry and the Neuroscience Research Center, Medical College of Wisconsin, Milwaukee Wisconsin 53226.
Sokol V TodiFrom the Departments of Pharmacology and Neurology, Wayne State University School of Medicine, Detroit, Michigan 48201 and stodi@med.wayne.edu.
Wayne State University · USMedical College of Wisconsin · US

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
Drosophila Transgenic RNAi Resource ProjectR01GM084947 · NIGMS · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2008 to 2019
$9.8M
Protection against Alzheimer's Disease proteins by novel ubiquitin processesR01NS086778 · NINDS · WAYNE STATE UNIVERSITY · PI Sokol Todi · 2014 to 2026
$4.9M
Protein fate in neurodegeneration: Investigations of novel regulatory mechanismsR00NS073936 · NINDS · MEDICAL COLLEGE OF WISCONSIN · PI SCAGLIONE, KENNETH MATTHEW · 2014 to 2016
$741k
NIGMS NIH HHS R01 GM084947NIH HHS P40 OD018537NINDS NIH HHS R00 NS073936NINDS NIH HHS R01 NS086778
6 · The paper itself

Abstract

Ubiquitination is a post-translational modification that regulates most cellular pathways and processes, including degradation of proteins by the proteasome. Substrate ubiquitination is controlled at various stages, including through its reversal by deubiquitinases (DUBs). A critical outcome of this process is the recycling of monoubiquitin. One DUB whose function has been proposed to include monoubiquitin recycling is USP5. Here, we investigated whether Drosophila USP5 is important for maintaining monoubiquitin in vivo We found that the fruit fly orthologue of USP5 has catalytic preferences similar to its human counterpart and that this DUB is necessary during fly development. Our biochemical and genetic experiments indicate that reduction of USP5 does not lead to monoubiquitin depletion in developing flies. Also, introduction of exogenous ubiquitin does not suppress developmental lethality caused by loss of endogenous USP5. Our work indicates that a primary physiological role of USP5 is not to recycle monoubiquitin for reutilization, but that it may involve disassembly of conjugated ubiquitin to maintain proteasome function.

Indexed as

AnimalsDrosophila melanogasterDrosophila ProteinsProteasome Endopeptidase ComplexUbiquitinUbiquitinationUbiquitin-Specific ProteasesDrosophila ProteinsProteasome Endopeptidase ComplexUbiquitinUbiquitin-Specific ProteasesUSP5 protein, Drosophila70 kilodalton heat shock protein (Hsp70)CHIPdeubiquitylation (deubiquitination)Drosophilapost-translational modification (PTM)proteaseproteasomeubiquitin

Identifiers

PMID26917723
PMCPMC4861482
OpenAlexW2285209545

What OpenQuestion holds

Textmetadata
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.