Evidence map›Paper›PMID 35468895›Full record

ArticleNature communications2022

Reduced chromatin accessibility correlates with resistance to Notch activation.

Jelle van den Ameele, Robert Krautz, Seth W Cheetham, Alex P A Donovan, Oriol Llorà-Batlle, Rebecca Yakob, Andrea H Brand

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  11. Notch Signaling Plays a Dual Role in Regulating the Neuron-to-Oligodendrocyte Switch in the Developing Dorsal Forebrain.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
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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

7 authors at 3 institutions in 3 countries.

Jelle van den Ameele *The Gurdon Institute and Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.ORCID 0000-0002-2744-0810
Robert Krautz *The Gurdon Institute and Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.ORCID 0000-0003-0457-1348
Seth W Cheetham *The Gurdon Institute and Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.ORCID 0000-0001-6428-3175
Alex P A DonovanThe Gurdon Institute and Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
Oriol Llorà-BatlleThe Gurdon Institute and Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.ORCID 0000-0002-8424-9705
Rebecca YakobThe Gurdon Institute and Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.ORCID 0000-0003-4275-5519
Andrea H BrandThe Gurdon Institute and Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK. a.brand@gurdon.cam.ac.uk.ORCID 0000-0002-2089-6954
University of Cambridge · GBThe University of Queensland · AUUniversity of Copenhagen · DK

Funding

Cancer Research UK C6946/A24843Wellcome Trust 103792Wellcome Trust 103792/Z/14/ZWellcome Trust 105839Wellcome Trust 105839/Z/14/ZWellcome Trust 203144/A/16/Z
6 · The paper itself

Abstract

The Notch signalling pathway is a master regulator of cell fate transitions in development and disease. In the brain, Notch promotes neural stem cell (NSC) proliferation, regulates neuronal migration and maturation and can act as an oncogene or tumour suppressor. How NOTCH and its transcription factor RBPJ activate distinct gene regulatory networks in closely related cell types in vivo remains to be determined. Here we use Targeted DamID (TaDa), requiring only thousands of cells, to identify NOTCH and RBPJ binding in NSCs and their progeny in the mouse embryonic cerebral cortex in vivo. We find that NOTCH and RBPJ associate with a broad network of NSC genes. Repression of NSC-specific Notch target genes in intermediate progenitors and neurons correlates with decreased chromatin accessibility, suggesting that chromatin compaction may contribute to restricting NOTCH-mediated transactivation.

Indexed as

ChromatinNeural Stem CellsAnimalsCell DifferentiationMiceReceptors, NotchSignal TransductionChromatinReceptors, Notch

Identifiers

PMID35468895
PMCPMC9039071
OpenAlexW4224926149

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.