Evidence map›Paper›PMID 29155828›Full record

ArticlePLoS genetics2017

Role of co-repressor genomic landscapes in shaping the Notch response.

Stephen K K Chan, Gustavo Cerda-Moya, Robert Stojnic, Kat Millen, Bettina Fischer, Silvie Fexova, Lenka Skalska, Maria Gomez-Lamarca, Zoe Pillidge, Steven Russell and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  7. Positive autoregulation ofDevelopment (Cambridge, England) · 2020
    Article
  8. Article
  9. An RBPJ-Cells · 2019
    Article
  10. 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
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 1 institution in 1 country.

Stephen K K ChanDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Gustavo Cerda-MoyaDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Robert StojnicDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.ORCID http://orcid.org/0000-0002-6458-0273
Kat MillenDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Bettina FischerCambridge Systems Biology Centre, University of Cambridge, Cambridge, United Kingdom.ORCID http://orcid.org/0000-0003-2821-6287
Silvie FexovaDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Lenka SkalskaDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Maria Gomez-LamarcaDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Zoe PillidgeDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Steven RussellCambridge Systems Biology Centre, University of Cambridge, Cambridge, United Kingdom.ORCID http://orcid.org/0000-0003-0546-3031
Sarah J BrayDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.ORCID http://orcid.org/0000-0002-1642-599X
University of Cambridge · GB

Funding

Medical Research Council G0800034Medical Research Council MR/L007177/1
6 · The paper itself

Abstract

Repressors are frequently deployed to limit the transcriptional response to signalling pathways. For example, several co-repressors interact directly with the DNA-binding protein CSL and are proposed to keep target genes silenced in the absence of Notch activity. However, the scope of their contributions remains unclear. To investigate co-repressor activity in the context of this well defined signalling pathway, we have analysed the genome-wide binding profile of the best-characterized CSL co-repressor in Drosophila, Hairless, and of a second CSL interacting repressor, SMRTER. As predicted there was significant overlap between Hairless and its CSL DNA-binding partner, both in Kc cells and in wing discs, where they were predominantly found in chromatin with active enhancer marks. However, while the Hairless complex was widely present at some Notch regulated enhancers in the wing disc, no binding was detected at others, indicating that it is not essential for silencing per se. Further analysis of target enhancers confirmed differential requirements for Hairless. SMRTER binding significantly overlapped with Hairless, rather than complementing it, and many enhancers were apparently co-bound by both factors. Our analysis indicates that the actions of Hairless and SMRTER gate enhancers to Notch activity and to Ecdysone signalling respectively, to ensure that the appropriate levels and timing of target gene expression are achieved.

Indexed as

AnimalsBinding SitesCo-Repressor ProteinsDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsEcdysoneGene Expression Regulation, DevelopmentalGenomicsProtein BindingReceptors, NotchRegulatory Sequences, Nucleic AcidRepressor ProteinsSignal TransductionTranscription FactorsCo-Repressor ProteinsDNA-Binding ProteinsDrosophila ProteinsEcdysoneH protein, DrosophilaReceptors, NotchRepressor ProteinsSmr protein, DrosophilaTranscription Factors

Identifiers

PMID29155828
PMCPMC5714389
OpenAlexW2769811918

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.