Evidence map›Paper›PMID 28378812›Full record

ArticleNature communications2017

EcR recruits dMi-2 and increases efficiency of dMi-2-mediated remodelling to constrain transcription of hormone-regulated genes.

Judith Kreher, Kristina Kovač, Karim Bouazoune, Igor Mačinković, Anna Luise Ernst, Erik Engelen, Roman Pahl, Florian Finkernagel, Magdalena Murawska, Ikram Ullah and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Coregulators Reside withinInternational journal of molecular sciences · 2023
    Article
  3. Article
  4. Opportunistic binding of EcR to open chromatin drives tissue-specific developmental responses.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  5. Article
  6. Direct and indirect gene repression by the ecdysone cascade during mosquito reproductive cycle.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Direct and widespread role for the nuclear receptor EcR in mediating the response to ecdysone inProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  12. Article
  13. Article
  14. 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

11 authors at 2 institutions in 1 country.

Judith KreherInstitute of Molecular Biology and Tumour Research, Philipps University Marburg, Marburg 35037, Germany.
Kristina KovačInstitute of Molecular Biology and Tumour Research, Philipps University Marburg, Marburg 35037, Germany.
Karim BouazouneInstitute of Molecular Biology and Tumour Research, Philipps University Marburg, Marburg 35037, Germany.
Igor MačinkovićInstitute of Molecular Biology and Tumour Research, Philipps University Marburg, Marburg 35037, Germany.
Anna Luise ErnstInstitute of Molecular Biology and Tumour Research, Philipps University Marburg, Marburg 35037, Germany.
Erik EngelenInstitute of Molecular Biology and Tumour Research, Philipps University Marburg, Marburg 35037, Germany.
Roman PahlInstitute of Medical Biometry and Epidemiology, Philipps University Marburg, Marburg 35037, Germany.
Florian FinkernagelCenter for Tumour Biology and Immunology, Philipps University Marburg, Marburg 35043, Germany.
Magdalena MurawskaInstitute of Molecular Biology and Tumour Research, Philipps University Marburg, Marburg 35037, Germany.
Ikram UllahInstitute of Molecular Biology and Tumour Research, Philipps University Marburg, Marburg 35037, Germany.
Alexander BrehmInstitute of Molecular Biology and Tumour Research, Philipps University Marburg, Marburg 35037, Germany.
Philipps University of Marburg · DEInstitute of Molecular Biology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene regulation by steroid hormones plays important roles in health and disease. In Drosophila, the hormone ecdysone governs transitions between key developmental stages. Ecdysone-regulated genes are bound by a heterodimer of ecdysone receptor (EcR) and Ultraspiracle. According to the bimodal switch model, steroid hormone receptors recruit corepressors in the absence of hormone and coactivators in its presence. Here we show that the nucleosome remodeller dMi-2 is recruited to ecdysone-regulated genes to limit transcription. Contrary to the prevalent model, recruitment of the dMi-2 corepressor increases upon hormone addition to constrain gene activation through chromatin remodelling. Furthermore, EcR and dMi-2 form a complex that is devoid of Ultraspiracle. Unexpectedly, EcR contacts the dMi-2 ATPase domain and increases the efficiency of dMi-2-mediated nucleosome remodelling. This study identifies a non-canonical EcR-corepressor complex with the potential for a direct regulation of ATP-dependent nucleosome remodelling by a nuclear hormone receptor.

Indexed as

Adenosine TriphosphatasesAnimalsAutoantigensChromatinDrosophilaDrosophila ProteinsEcdysoneGene Expression RegulationKineticsReceptors, SteroidTranscriptional ActivationTranscription, GeneticAdenosine TriphosphatasesAutoantigensChromatinDrosophila ProteinsEcdysoneecdysone receptorMi-2 protein, DrosophilaReceptors, Steroid

Identifiers

PMID28378812
PMCPMC5382322
OpenAlexW2604132347

What OpenQuestion holds

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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.