Evidence map›Paper›PMID 26573619›Full record

ArticleBMC genomics2015

EWS and FUS bind a subset of transcribed genes encoding proteins enriched in RNA regulatory functions.

Yonglun Luo, Jenny Blechingberg, Ana Miguel Fernandes, Shengting Li, Tue Fryland, Anders D Børglum, Lars Bolund, Anders Lade Nielsen

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. METTL3-mediated SNHG1 mFrontiers in oncology · 2025
    Article
  5. International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Biomolecules · 2023
    Review
  11. Article
  12. Article
  13. A subset of epithelioid and spindle cell rhabdomyosarcomas is associated with TFCP2 fusions and common ALK upregulation.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2020
    Article
  14. TheJournal of virology · 2020
    Article
  15. Article
  16. Article
  17. ALS mutations of FUS suppress protein translation and disrupt the regulation of nonsense-mediated decay.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  18. Article
  19. 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

8 authors at 2 institutions in 1 country.

Yonglun LuoDepartment of Biomedicine, Aarhus University, The Bartholin Building, Aarhus, DK-8000, Denmark. alun@biomed.au.dk.
Jenny BlechingbergDepartment of Biomedicine, Aarhus University, The Bartholin Building, Aarhus, DK-8000, Denmark. Jenny.Friis@rsyd.dk.
Ana Miguel FernandesDepartment of Biomedicine, Aarhus University, The Bartholin Building, Aarhus, DK-8000, Denmark. anamiguel.fernandes@mdc-berlin.de.
Shengting LiDepartment of Biomedicine, Aarhus University, The Bartholin Building, Aarhus, DK-8000, Denmark. shengting@biomed.au.dk.
Tue FrylandDepartment of Biomedicine, Aarhus University, The Bartholin Building, Aarhus, DK-8000, Denmark. tue@biomed.au.dk.
Anders D BørglumDepartment of Biomedicine, Aarhus University, The Bartholin Building, Aarhus, DK-8000, Denmark. anders@biomed.au.dk.
Lars BolundDepartment of Biomedicine, Aarhus University, The Bartholin Building, Aarhus, DK-8000, Denmark. bolund@biomed.au.dk.
Anders Lade NielsenDepartment of Biomedicine, Aarhus University, The Bartholin Building, Aarhus, DK-8000, Denmark. aln@biomed.au.dk.
Aarhus University · DKLundbeck Foundation · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFUS (TLS) and EWS (EWSR1) belong to the FET-protein family of RNA and DNA binding proteins. FUS and EWS are structurally and functionally related and participate in transcriptional regulation and RNA processing. FUS and EWS are identified in translocation generated cancer fusion proteins and involved in the human neurological diseases amyotrophic lateral sclerosis and fronto-temporal lobar degeneration.

resultsTo determine the gene regulatory functions of FUS and EWS at the level of chromatin, we have performed chromatin immunoprecipitation followed by next generation sequencing (ChIP-seq). Our results show that FUS and EWS bind to a subset of actively transcribed genes, that binding often is downstream the poly(A)-signal, and that binding overlaps with RNA polymerase II. Functional examinations of selected target genes identified that FUS and EWS can regulate gene expression at different levels. Gene Ontology analyses showed that FUS and EWS target genes preferentially encode proteins involved in regulatory processes at the RNA level.

conclusionsThe presented results yield new insights into gene interactions of EWS and FUS and have identified a set of FUS and EWS target genes involved in pathways at the RNA regulatory level with potential to mediate normal and disease-associated functions of the FUS and EWS proteins.

Indexed as

ChromatinChromatin ImmunoprecipitationHEK293 CellsHumansProtein BindingRNARNA-Binding Protein EWSRNA-Binding Protein FUSRNA Processing, Post-TranscriptionalTranscription, GeneticChromatinFUS protein, humanRNARNA-Binding Protein EWSRNA-Binding Protein FUS

Identifiers

PMID26573619
PMCPMC4647676
OpenAlexW2178875635

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.