Evidence map›Paper›PMID 17023429›Full record

ArticleThe Journal of biological chemistry2006

BRG1 chromatin remodeling activity is required for efficient chromatin binding by repressor element 1-silencing transcription factor (REST) and facilitates REST-mediated repression.

Lezanne Ooi, Nikolai D Belyaev, Katsuhide Miyake, Ian C Wood, Noel J Buckley

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

57 citing papers in PubMed, 106 citations in OpenAlex.

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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

5 authors at 2 institutions in 2 countries.

Lezanne OoiInstitute of Membrane and Systems Biology, University of Leeds, Leeds LS2 9JT, United Kingdom. L.Ooi@leeds.ac.uk
Nikolai D Belyaev
Katsuhide Miyake
Ian C Wood
Noel J Buckley
University of Leeds · GBNagoya University · JP

Funding

Wellcome Trust 075168Wellcome Trust 076391
6 · The paper itself

Abstract

Chromatin remodeling enzymes such as SWI/SNF use the hydrolysis of ATP to power the movement of nucleosomes with respect to DNA. BRG1, one of the ATPases of the SWI/SNF complex, can be recruited by both activators and repressors, although the precise role of BRG1 in mechanisms of repression has thus far remained unclear. One transcription factor that recruits BRG1 as a corepressor is the repressor element 1-silencing transcription factor (REST). Here we address for the first time the mechanism of BRG1 activity in gene repression. We found that BRG1 enhanced REST-mediated repression at some REST target genes by increasing the interaction of REST with the local chromatin at its binding sites. Furthermore, REST-chromatin interactions, mediated by BRG1, were enhanced following an increase in histone acetylation in a manner dependent on the BRG1 bromodomain. Our data suggest that BRG1 facilitates REST repression by increasing the interaction between REST and chromatin. Such a mechanism may be applicable to other transcriptional repressors that utilize BRG1.

Indexed as

AcetylationAdenosine TriphosphateBinding SitesCell LineCell NucleusChromatinDNA HelicasesHistonesHumansHydroxamic AcidsNuclear ProteinsPlasmidsProtein BindingRE1-Silencing Transcription FactorRepressor ProteinsTranscription FactorsAdenosine TriphosphateChromatinDNA HelicasesHistonesHydroxamic AcidsNuclear ProteinsRE1-Silencing Transcription FactorRepressor ProteinsSMARCA4 protein, humanTranscription Factorstrichostatin A

Identifiers

PMID17023429
PMCPMC1820614
OpenAlexW2029925836

What OpenQuestion holds

Textmetadata
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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.