Evidence map›Paper›PMID 27694995›Full record

ArticleNature neuroscience2016

Chd8 mediates cortical neurogenesis via transcriptional regulation of cell cycle and Wnt signaling.

Omer Durak, Fan Gao, Yea Jin Kaeser-Woo, Richard Rueda, Anthony J Martorell, Alexi Nott, Carol Y Liu, L Ashley Watson, Li-Huei Tsai

Open access · greenAbstract read
In one paragraph

Article in Nature neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 152 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
152citing papers in PubMed, 2 pooled it
24.9field-weighted citation impact, top 1% 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

152 citing papers in PubMed, 2 syntheses or guidelines pooled it, 240 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Molecular Acrobats: How CHD Remodelers Shape the Genetic Playground to License Cell Identity.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
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  10. Chromodomain helicase DNA-binding proteins and orofacial cleft.Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2026
    Review
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92 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Omer DurakPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts USA.
Fan GaoPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts USA.
Yea Jin Kaeser-WooPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts USA.
Richard RuedaPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts USA.
Anthony J MartorellPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts USA.
Alexi NottPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts USA.
Carol Y LiuPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts USA.
L Ashley WatsonPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts USA.
Li-Huei TsaiPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts USA.
Massachusetts Institute of Technology · USBroad Institute · USInstitute of Cognitive and Brain Sciences · US

Funding

Novel technologies for nontoxic transsynaptic tracingU01MH106018 · NIMH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI WICKERSHAM, IAN R · 2014 to 2016
$2.5M
NIMH NIH HHS U01 MH106018
6 · The paper itself

Abstract

De novo mutations in CHD8 are strongly associated with autism spectrum disorder, but the basic biology of CHD8 remains poorly understood. Here we report that Chd8 knockdown during cortical development results in defective neural progenitor proliferation and differentiation that ultimately manifests in abnormal neuronal morphology and behaviors in adult mice. Transcriptome analysis revealed that while Chd8 stimulates the transcription of cell cycle genes, it also precludes the induction of neural-specific genes by regulating the expression of PRC2 complex components. Furthermore, knockdown of Chd8 disrupts the expression of key transducers of Wnt signaling, and enhancing Wnt signaling rescues the transcriptional and behavioral deficits caused by Chd8 knockdown. We propose that these roles of Chd8 and the dynamics of Chd8 expression during development help negotiate the fine balance between neural progenitor proliferation and differentiation. Together, these observations provide new insights into the neurodevelopmental role of Chd8.

Indexed as

NeurogenesisTranscription, GeneticAnimalsAutism Spectrum DisorderCell CycleCell DifferentiationCell DivisionDNA-Binding ProteinsFemaleGene Expression Regulation, DevelopmentalMiceNeural Stem CellsWnt Signaling PathwayDNA-Binding Proteinsduplin protein, mouse

Identifiers

PMID27694995
PMCPMC5386887
OpenAlexW2528582931

What OpenQuestion holds

Textmetadata
LicenceTDM
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.