Evidence map›Paper›PMID 26934049›Full record

ArticlePloS one2016

Expression Atlas of the Deubiquitinating Enzymes in the Adult Mouse Retina, Their Evolutionary Diversification and Phenotypic Roles.

Mariona Esquerdo, Xavier Grau-Bové, Alejandro Garanto, Vasileios Toulis, Sílvia Garcia-Monclús, Erica Millo, Ma José López-Iniesta, Víctor Abad-Morales, Iñaki Ruiz-Trillo, Gemma Marfany

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Candidate Genetic Modifiers for RPGR Retinal Degeneration.Investigative ophthalmology & visual science · 2020
    Article
  4. Article
  5. Article
  6. 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

10 authors at 5 institutions in 1 country.

Mariona EsquerdoDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
Xavier Grau-BovéDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
Alejandro GarantoDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
Vasileios ToulisDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
Sílvia Garcia-MonclúsDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
Erica MilloDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
Ma José López-IniestaDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
Víctor Abad-MoralesDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
Iñaki Ruiz-TrilloDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
Gemma MarfanyDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
Universitat de Barcelona · ESCentre for Biomedical Network Research on Rare Diseases · ESInstitució Catalana de Recerca i Estudis Avançats · ESInstituto de Salud Carlos III · ESPompeu Fabra University · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ubiquitination is a relevant cell regulatory mechanism to determine protein fate and function. Most data has focused on the role of ubiquitin as a tag molecule to target substrates to proteasome degradation, and on its impact in the control of cell cycle, protein homeostasis and cancer. Only recently, systematic assays have pointed to the relevance of the ubiquitin pathway in the development and differentiation of tissues and organs, and its implication in hereditary diseases. Moreover, although the activity and composition of ubiquitin ligases has been largely addressed, the role of the deubiquitinating enzymes (DUBs) in specific tissues, such as the retina, remains mainly unknown. In this work, we undertook a systematic analysis of the transcriptional levels of DUB genes in the adult mouse retina by RT-qPCR and analyzed the expression pattern by in situ hybridization and fluorescent immunohistochemistry, thus providing a unique spatial reference map of retinal DUB expression. We also performed a systematic phylogenetic analysis to understand the origin and the presence/absence of DUB genes in the genomes of diverse animal taxa that represent most of the known animal diversity. The expression landscape obtained supports the potential subfunctionalization of paralogs in those families that expanded in vertebrates. Overall, our results constitute a reference framework for further characterization of the DUB roles in the retina and suggest new candidates for inherited retinal disorders.

Indexed as

UbiquitinationAnimalsGene Expression RegulationImmunohistochemistryIn Situ HybridizationMiceMice, Inbred C57BLPhylogenyRetinaReverse Transcriptase Polymerase Chain Reaction

Identifiers

PMID26934049
PMCPMC4774998
OpenAlexW2294587004

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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.