Evidence map›Paper›PMID 38149716›Full record

ArticleBiology open2024

The Nucleosome Remodelling and Deacetylation complex coordinates the transcriptional response to lineage commitment in pluripotent cells.

Bertille Montibus, Ramy Ragheb, Evangelia Diamanti, Sara-Jane Dunn, Nicola Reynolds, Brian Hendrich

Open access · goldAbstract read
In one paragraph

Article in Biology open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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  3. Review
  4. 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 2 institutions in 1 country.

Bertille MontibusWellcome - MRC Stem Cell Institute, University of Cambridge, Cambridge CB2 0AW, United Kingdom.ORCID 0000-0002-6895-3954
Ramy RaghebWellcome - MRC Stem Cell Institute, University of Cambridge, Cambridge CB2 0AW, United Kingdom.ORCID 0000-0001-5892-1767
Evangelia DiamantiWellcome - MRC Stem Cell Institute, University of Cambridge, Cambridge CB2 0AW, United Kingdom.
Sara-Jane DunnMicrosoft Research, 21 Station Road, Cambridge CB1 2FB, UK.ORCID 0000-0002-5964-1043
Nicola ReynoldsWellcome - MRC Stem Cell Institute, University of Cambridge, Cambridge CB2 0AW, United Kingdom.ORCID 0000-0003-1620-2750
Brian HendrichWellcome - MRC Stem Cell Institute, University of Cambridge, Cambridge CB2 0AW, United Kingdom.ORCID 0000-0002-0231-3073
Wellcome/MRC Cambridge Stem Cell Institute · GBMicrosoft Research (United Kingdom) · GB

Funding

Medical Research Council MC_PC_17230Medical Research Council MR/P019471/1Medical Research Council MR/R009759/1Wellcome TrustWellcome Trust 206291/Z/17/Z
6 · The paper itself

Abstract

As cells exit the pluripotent state and begin to commit to a specific lineage they must activate genes appropriate for that lineage while silencing genes associated with pluripotency and preventing activation of lineage-inappropriate genes. The Nucleosome Remodelling and Deacetylation (NuRD) complex is essential for pluripotent cells to successfully undergo lineage commitment. NuRD controls nucleosome density at regulatory sequences to facilitate transcriptional responses, and also has been shown to prevent unscheduled transcription (transcriptional noise) in undifferentiated pluripotent cells. How these activities combine to ensure cells engage a gene expression program suitable for successful lineage commitment has not been determined. Here, we show that NuRD is not required to silence all genes. Rather, it restricts expression of genes primed for activation upon exit from the pluripotent state, but maintains them in a transcriptionally permissive state in self-renewing conditions, which facilitates their subsequent activation upon exit from naïve pluripotency. We further show that NuRD coordinates gene expression changes, which acts to maintain a barrier between different stable states. Thus NuRD-mediated chromatin remodelling serves multiple functions, including reducing transcriptional noise, priming genes for activation and coordinating the transcriptional response to facilitate lineage commitment.

Indexed as

DNA-Binding ProteinsTranscription FactorsCell DifferentiationMi-2 Nucleosome Remodeling and Deacetylase ComplexNucleosomesDNA-Binding ProteinsMi-2 Nucleosome Remodeling and Deacetylase ComplexNucleosomesTranscription FactorsChromatinEmbryonic stem cellLineage commitmentMBD3NuRDTranscription

Identifiers

PMID38149716
PMCPMC10836651
OpenAlexW4390273787

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.