Evidence map›Paper›PMID 30389936›Full record

ArticleNature communications2018

NuRD-interacting protein ZFP296 regulates genome-wide NuRD localization and differentiation of mouse embryonic stem cells.

Susan L Kloet, Ino D Karemaker, Lisa van Voorthuijsen, Rik G H Lindeboom, Marijke P Baltissen, Raghu R Edupuganti, Deepani W Poramba-Liyanage, Pascal W T C Jansen, Michiel Vermeulen

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

16 citing papers in PubMed, 32 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

9 authors at 1 institution in 1 country.

Susan L KloetDepartment of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, 6500 HB, The Netherlands.ORCID http://orcid.org/0000-0001-9189-0640
Ino D KaremakerDepartment of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Oncode Institute, Radboud University Nijmegen, Nijmegen, 6500 HB, The Netherlands.ORCID http://orcid.org/0000-0002-6528-9330
Lisa van VoorthuijsenDepartment of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Oncode Institute, Radboud University Nijmegen, Nijmegen, 6500 HB, The Netherlands.ORCID http://orcid.org/0000-0003-4822-185X
Rik G H LindeboomDepartment of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Oncode Institute, Radboud University Nijmegen, Nijmegen, 6500 HB, The Netherlands.ORCID http://orcid.org/0000-0002-3660-504X
Marijke P BaltissenDepartment of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Oncode Institute, Radboud University Nijmegen, Nijmegen, 6500 HB, The Netherlands.
Raghu R EdupugantiDepartment of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, 6500 HB, The Netherlands.
Deepani W Poramba-LiyanageDepartment of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, 6500 HB, The Netherlands.ORCID http://orcid.org/0000-0003-3717-4787
Pascal W T C JansenDepartment of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Oncode Institute, Radboud University Nijmegen, Nijmegen, 6500 HB, The Netherlands.
Michiel VermeulenDepartment of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Oncode Institute, Radboud University Nijmegen, Nijmegen, 6500 HB, The Netherlands. michiel.vermeulen@science.ru.nl.ORCID http://orcid.org/0000-0003-0836-6894
Radboud University Nijmegen · NL

Funding

European Research Council 309384
6 · The paper itself

Abstract

The nucleosome remodeling and deacetylase (NuRD) complex plays an important role in gene expression regulation, stem cell self-renewal, and lineage commitment. However, little is known about the dynamics of NuRD during cellular differentiation. Here, we study these dynamics using genome-wide profiling and quantitative interaction proteomics in mouse embryonic stem cells (ESCs) and neural progenitor cells (NPCs). We find that the genomic targets of NuRD are highly dynamic during differentiation, with most binding occurring at cell-type specific promoters and enhancers. We identify ZFP296 as an ESC-specific NuRD interactor that also interacts with the SIN3A complex. ChIP-sequencing in Zfp296 knockout (KO) ESCs reveals decreased NuRD binding both genome-wide and at ZFP296 binding sites, although this has little effect on the transcriptome. Nevertheless, Zfp296 KO ESCs exhibit delayed induction of lineage-specific markers upon differentiation to embryoid bodies. In summary, we identify an ESC-specific NuRD-interacting protein which regulates genome-wide NuRD binding and cellular differentiation.

Indexed as

Cell DifferentiationGenomeAnimalsDNA-Binding ProteinsEnhancer Elements, GeneticGene Expression RegulationMi-2 Nucleosome Remodeling and Deacetylase ComplexMiceMice, KnockoutMouse Embryonic Stem CellsPromoter Regions, GeneticProtein BindingProtein TransportRepressor ProteinsSin3 Histone Deacetylase and Corepressor ComplexDNA-Binding ProteinsMi-2 Nucleosome Remodeling and Deacetylase ComplexRepressor ProteinsSIN3A transcription factorSin3 Histone Deacetylase and Corepressor Complexzinc finger protein 296, mouse

Identifiers

PMID30389936
PMCPMC6214896
OpenAlexW2898651882

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.