Evidence map›Paper›PMID 32647123›Full record

ArticleNature communications2020

The chromatin remodeling enzyme Chd4 regulates genome architecture in the mouse brain.

Jared V Goodman, Tomoko Yamada, Yue Yang, Lingchun Kong, Dennis Y Wu, Guoyan Zhao, Harrison W Gabel, Azad Bonni

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.3field-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

42 citing papers in PubMed, 58 citations in OpenAlex.

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  16. Cells and Molecules Underpinning Cannabis-Related Variations in Cortical Thickness during Adolescence.The Journal of neuroscience : the official journal of the Society for Neuroscience · 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

8 authors at 2 institutions in 2 countries.

Jared V GoodmanDepartment of Neuroscience, Washington University School of Medicine, St. Louis, MO, USA.ORCID http://orcid.org/0000-0003-2235-5673
Tomoko Yamada *Department of Neuroscience, Washington University School of Medicine, St. Louis, MO, USA.
Yue Yang *Department of Neuroscience, Washington University School of Medicine, St. Louis, MO, USA.
Lingchun KongDepartment of Neuroscience, Washington University School of Medicine, St. Louis, MO, USA.
Dennis Y WuDepartment of Neuroscience, Washington University School of Medicine, St. Louis, MO, USA.
Guoyan ZhaoDepartment of Neuroscience, Washington University School of Medicine, St. Louis, MO, USA.
Harrison W GabelDepartment of Neuroscience, Washington University School of Medicine, St. Louis, MO, USA.
Azad BonniDepartment of Neuroscience, Washington University School of Medicine, St. Louis, MO, USA. bonni@wustl.edu.ORCID http://orcid.org/0000-0003-1391-1500
Washington University in St. Louis · USNorthwestern University · US

Funding

SIGNAL TRANSDUCTION PATHWAYS REGULATING NEURON SURVIVALR01NS041021 · NINDS · WASHINGTON UNIVERSITY · PI GABEL, HARRISON W · 2001 to 2023
$7.7M
MECHANISMS OF EPIGENETIC REGULATION IN NERVOUS SYSTEM DEVELOPMENTR01MH117405 · NIMH · WASHINGTON UNIVERSITY · PI Harrison W Gabel · 2019 to 2026
$3.9M
Elucidating the Roles of Mbd3 during Cerebellar DevelopmentF30HD094447 · NICHD · WASHINGTON UNIVERSITY · PI GOODMAN, JARED VEGA · 2018 to 2020
$107k
NICHD NIH HHS F30 HD094447NIMH NIH HHS R01 MH117405NINDS NIH HHS R01 NS041021
6 · The paper itself

Abstract

The development and function of the brain require tight control of gene expression. Genome architecture is thought to play a critical regulatory role in gene expression, but the mechanisms governing genome architecture in the brain in vivo remain poorly understood. Here, we report that conditional knockout of the chromatin remodeling enzyme Chd4 in granule neurons of the mouse cerebellum increases accessibility of gene regulatory sites genome-wide in vivo. Conditional knockout of Chd4 promotes recruitment of the architectural protein complex cohesin preferentially to gene enhancers in granule neurons in vivo. Importantly, in vivo profiling of genome architecture reveals that conditional knockout of Chd4 strengthens interactions among developmentally repressed contact domains as well as genomic loops in a manner that tightly correlates with increased accessibility, enhancer activity, and cohesin occupancy at these sites. Collectively, our findings define a role for chromatin remodeling in the control of genome architecture organization in the mammalian brain.

Indexed as

Chromatin Assembly and DisassemblyGenomeAnimalsBrainCell Cycle ProteinsChromatinChromosomal Proteins, Non-HistoneChromosomes, MammalianCohesinsDNA HelicasesEnhancer Elements, GeneticEpigenesis, GeneticMice, KnockoutModels, GeneticProtein BindingCell Cycle ProteinsChromatinChromosomal Proteins, Non-HistoneCohesinsDNA HelicasesMi-2beta protein, mouse

Identifiers

PMID32647123
PMCPMC7347877
OpenAlexW3041221842

What OpenQuestion holds

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Registered trials

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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.