Evidence map›Paper›PMID 29779894›Full record

ArticleStem cell reports2018

Epigenetic Regulation by BAF Complexes Limits Neural Stem Cell Proliferation by Suppressing Wnt Signaling in Late Embryonic Development.

Huong Nguyen, Cemil Kerimoglu, Mehdi Pirouz, Linh Pham, Kamila A Kiszka, Godwin Sokpor, M Sadman Sakib, Joachim Rosenbusch, Ulrike Teichmann, Rho H Seong and 4 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

38 citing papers in PubMed, 59 citations in OpenAlex.

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  8. Chromatin remodeling in tissue stem cell fate determination.Cell regeneration (London, England) · 2024
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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

14 authors at 5 institutions in 2 countries.

Huong NguyenInstitute of Neuroanatomy, University Medical Center, Georg-August- University, 37075 Goettingen, Germany.
Cemil KerimogluDepartment of Psychiatry and Psychotherapy, University Medical Center, Georg- August-University Goettingen, 37077 Goettingen, Germany; Department for Systems Medicine and Epigenetics, German Center for Neurodegenerative Diseases, 37075 Goettingen, Germany.
Mehdi PirouzMax-Planck-Institute for Biophysical Chemistry, 37077 Goettingen, Germany.
Linh PhamInstitute of Neuroanatomy, University Medical Center, Georg-August- University, 37075 Goettingen, Germany.
Kamila A KiszkaInstitute of Neuroanatomy, University Medical Center, Georg-August- University, 37075 Goettingen, Germany; DFG Center for Nanoscale Microscopy & Molecular Physiology of the Brain (CNMPB), 37075 Goettingen, Germany.
Godwin SokporInstitute of Neuroanatomy, University Medical Center, Georg-August- University, 37075 Goettingen, Germany.
M Sadman SakibDepartment of Psychiatry and Psychotherapy, University Medical Center, Georg- August-University Goettingen, 37077 Goettingen, Germany; Department for Systems Medicine and Epigenetics, German Center for Neurodegenerative Diseases, 37075 Goettingen, Germany.
Joachim RosenbuschInstitute of Neuroanatomy, University Medical Center, Georg-August- University, 37075 Goettingen, Germany.
Ulrike TeichmannMax-Planck-Institute for Biophysical Chemistry, 37077 Goettingen, Germany.
Rho H SeongDepartment of Biological Sciences, Institute of Molecular Biology and Genetics, Research Center for Functional Cellulomics, Seoul National University, Seoul 151- 742, Korea.
Anastassia StoykovaMax-Planck-Institute for Biophysical Chemistry, 37077 Goettingen, Germany; DFG Center for Nanoscale Microscopy & Molecular Physiology of the Brain (CNMPB), 37075 Goettingen, Germany.
Andre FischerDepartment of Psychiatry and Psychotherapy, University Medical Center, Georg- August-University Goettingen, 37077 Goettingen, Germany; Department for Systems Medicine and Epigenetics, German Center for Neurodegenerative Diseases, 37075 Goettingen, Germany.
Jochen F StaigerInstitute of Neuroanatomy, University Medical Center, Georg-August- University, 37075 Goettingen, Germany; DFG Center for Nanoscale Microscopy & Molecular Physiology of the Brain (CNMPB), 37075 Goettingen, Germany.
Tran TuocInstitute of Neuroanatomy, University Medical Center, Georg-August- University, 37075 Goettingen, Germany; DFG Center for Nanoscale Microscopy & Molecular Physiology of the Brain (CNMPB), 37075 Goettingen, Germany. Electronic address: tran.tuoc@med.uni-goettingen.de.
University of Göttingen · DEMax Planck Institute for Biophysical Chemistry · DEGerman Center for Neurodegenerative Diseases · DENanoscale Microscopy and Molecular Physiology of the Brain Cluster of Excellence 171 — DFG Research Center 103 · DESeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During early cortical development, neural stem cells (NSCs) divide symmetrically to expand the progenitor pool, whereas, in later stages, NSCs divide asymmetrically to self-renew and produce other cell types. The timely switch from such proliferative to differentiative division critically determines progenitor and neuron numbers. However, the mechanisms that limit proliferative division in late cortical development are not fully understood. Here, we show that the BAF (mSWI/SNF) complexes restrict proliferative competence and promote neuronal differentiation in late corticogenesis. Inactivation of BAF complexes leads to H3K27me3-linked silencing of neuronal differentiation-related genes, with concurrent H3K4me2-mediated activation of proliferation-associated genes via de-repression of Wnt signaling. Notably, the deletion of BAF complexes increased proliferation of neuroepithelial cell-like NSCs, impaired neuronal differentiation, and exerted a Wnt-dependent effect on neocortical and hippocampal development. Thus, these results demonstrate that BAF complexes act as both activators and repressors to control global epigenetic and gene expression programs in late corticogenesis.

Indexed as

Epigenesis, GeneticWnt Signaling PathwayAnimalsCell DifferentiationCell ProliferationChromatin Assembly and DisassemblyChromosomal Proteins, Non-HistoneEmbryonic DevelopmentFluorescent Antibody TechniqueGene Expression Regulation, DevelopmentalGene Knockout TechniquesHippocampusMiceNeural Stem CellsNeurogenesisNeuronsChromosomal Proteins, Non-HistoneRibonucleoproteinsBAF (mSWI/SNF) complexeschromatin remodelingcortical developmentepigeneticsH3K27me3H3K4me2hippocampal developmentneural stem cellsneurogenesis

Identifiers

PMID29779894
PMCPMC5993560
OpenAlexW2803438168

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.