Evidence map›Paper›PMID 20062082›Full record

ArticleOncogene2010

The E3 ubiquitin ligase complex component COP1 regulates PEA3 group member stability and transcriptional activity.

J-L Baert, D Monte, K Verreman, C Degerny, L Coutte, Y de Launoit

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

37 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. ETS factors in prostate cancer.Cancer letters · 2022
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. The Journal of biological chemistry · 2019
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Transcription factor Etv5 is essential for the maintenance of alveolar type II cells.Proceedings of the National Academy of Sciences of the United States of America · 2017
    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 3 institutions in 1 country.

J-L BaertCNRS UMR 8161, Institut de Biologie de Lille, Université de Lille-Nord de France, Institut Pasteur de Lille, Lille Cedex 59021, France. jean-luc.baert@ibl.fr
D Monte
K Verreman
C Degerny
L Coutte
Y de Launoit
Centre National de la Recherche Scientifique · FRInstitut Pasteur de Lille · FRUniversité de Lille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we report that the PEA3 group members interact with the mammalian really interesting new gene (RING) E3 ubiquitin ligase constitutive photomorphogenetic 1 (COP1), which mediates ubiquitylation and subsequent proteasome degradation of the p53 and c-Jun transcription factors. This interaction is mediated by the central region of COP1 including the coiled-coil domain and two COP1-interacting consensus motifs localized in the well-conserved N-terminal transactivation domain of the PEA3 group members. At the transcriptional level, COP1 reduces the transcriptional activity of ERM and the two other PEA3 group proteins on Ets-responsive reporter genes; this effect being dependent on the RING domain of COP1 and the two COP1-interacting motifs of ERM. Reduced transcriptional activity was, however, not related to COP1-induced changes in ERM stability. In fact, increased ubiquitylation and subsequent proteasome-mediated degradation of ERM is achieved only when COP1 is expressed with DET1, a key COP1 partner within the ubiquitylation complex. Conversely, we show that the depletion of COP1 or DET1 by small interference RNA (siRNA) in U2OS cells stabilizes endogenous ERM whereas only COP1 knockdown enhances expression of ICAM-1, a gene regulated by this transcription factor. These results indicate that COP1 is a complex regulator of ERM and the two other PEA3 group members.

Indexed as

Transcription, GeneticAmino Acid SequenceAnimalsChlorocebus aethiopsConserved SequenceCOS CellsDNA-Binding ProteinsGene Expression Regulation, NeoplasticGenetic VariationHomeostasisHumansMolecular Sequence DataNeoplasmsRNA InterferenceRNA, Small InterferingSequence AlignmentCOP1 protein, humanDNA-Binding ProteinsETV1 protein, humanRNA, Small InterferingTrans-ActivatorsTranscription FactorsUbiquitin-Protein Ligases

Identifiers

PMID20062082
OpenAlexW2079126104

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.