Evidence map›Paper›PMID 30849367›Full record

ArticleCell stem cell2019

Mapping the Global Chromatin Connectivity Network for Sox2 Function in Neural Stem Cell Maintenance.

Jessica A Bertolini, Rebecca Favaro, Yanfen Zhu, Miriam Pagin, Chew Yee Ngan, Chee Hong Wong, Harianto Tjong, Marit W Vermunt, Ben Martynoga, Cristiana Barone and 13 more

Open access · hybridAbstract read
In one paragraph

Article in Cell stem cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

62 citing papers in PubMed, 96 citations in OpenAlex.

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2 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 8 institutions in 6 countries.

Jessica A BertoliniDepartment of Biotechnology and Biosciences, University Milano-Bicocca, 20126 Milano, Italy.
Rebecca FavaroDepartment of Biotechnology and Biosciences, University Milano-Bicocca, 20126 Milano, Italy.
Yanfen ZhuThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Miriam PaginDepartment of Biotechnology and Biosciences, University Milano-Bicocca, 20126 Milano, Italy.
Chew Yee NganThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Chee Hong WongThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Harianto TjongThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Marit W VermuntHubrecht Institute-KNAW and University Medical Center Utrecht 3584CT, Utrecht, the Netherlands.
Ben MartynogaThe Francis Crick Institute, Midland Road, London NW 1AT, UK.
Cristiana BaroneDepartment of Biotechnology and Biosciences, University Milano-Bicocca, 20126 Milano, Italy.
Jessica MarianiDepartment of Biotechnology and Biosciences, University Milano-Bicocca, 20126 Milano, Italy.
Marcos Julián CardozoCentro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid and Ciber de Enfermedades Raras (CIBERER), ISCIII Madrid, Spain.
Noemi TabaneraCentro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid and Ciber de Enfermedades Raras (CIBERER), ISCIII Madrid, Spain.
Federico ZambelliDepartment of Biosciences, University of Milano, 20133 Milano, Italy.
Sara MercurioDepartment of Biotechnology and Biosciences, University Milano-Bicocca, 20126 Milano, Italy.
Sergio OttolenghiDepartment of Biotechnology and Biosciences, University Milano-Bicocca, 20126 Milano, Italy.
Paul RobsonThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA; Stem Cell and Regenerative Biology, Genome Institute of Singapore, Singapore.
Menno P CreyghtonHubrecht Institute-KNAW and University Medical Center Utrecht 3584CT, Utrecht, the Netherlands.
Paola BovolentaCentro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid and Ciber de Enfermedades Raras (CIBERER), ISCIII Madrid, Spain.
Giulio PavesiDepartment of Biosciences, University of Milano, 20133 Milano, Italy.
Francois GuillemotThe Francis Crick Institute, Midland Road, London NW 1AT, UK.
Silvia K NicolisDepartment of Biotechnology and Biosciences, University Milano-Bicocca, 20126 Milano, Italy. Electronic address: silvia.nicolis@unimib.it.
Chia-Lin WeiThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA. Electronic address: chia-lin.wei@jax.org.
University of Milano-Bicocca · ITJackson Laboratory · USHubrecht Institute for Developmental Biology and Stem Cell Research · NLInstituto de Salud Carlos III · ESThe Francis Crick Institute · GBUniversity of Milan · ITGenome Institute of Singapore · SGUniversidad Autónoma de Madrid · ES

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
Comprehensive Mapping of Long-Range Chromatin Interactions in Humanand Mouse GenomesUM1HG009409 · NHGRI · JACKSON LABORATORY · PI LEE, CHARLES · 2017 to 2021
$9.8M
Nucleome Positioning System for Spatiotemporal Genome Organization and RegulationU54DK107967 · NIDDK · JACKSON LABORATORY · PI WEI, CHIA-LIN · 2015 to 2019
$3.6M
Biotechnology and Biological Sciences Research Council BB/K005316/1Cancer Research UK FC0010089Medical Research Council FC0010089NCI NIH HHS P30 CA034196NHGRI NIH HHS UM1 HG009409NIDDK NIH HHS U54 DK107967Wellcome TrustWellcome Trust FC0010089
6 · The paper itself

Abstract

The SOX2 transcription factor is critical for neural stem cell (NSC) maintenance and brain development. Through chromatin immunoprecipitation (ChIP) and chromatin interaction analysis (ChIA-PET), we determined genome-wide SOX2-bound regions and Pol II-mediated long-range chromatin interactions in brain-derived NSCs. SOX2-bound DNA was highly enriched in distal chromatin regions interacting with promoters and carrying epigenetic enhancer marks. Sox2 deletion caused widespread reduction of Pol II-mediated long-range interactions and decreased gene expression. Genes showing reduced expression in Sox2-deleted cells were significantly enriched in interactions between promoters and SOX2-bound distal enhancers. Expression of one such gene, Suppressor of Cytokine Signaling 3 (Socs3), rescued the self-renewal defect of Sox2-ablated NSCs. Our work identifies SOX2 as a major regulator of gene expression through connections to the enhancer network in NSCs. Through the definition of such a connectivity network, our study shows the way to the identification of genes and enhancers involved in NSC maintenance and neurodevelopmental disorders.

Indexed as

AnimalsCells, CulturedChromatinGene Regulatory NetworksMiceMice, KnockoutMice, TransgenicMutationNeural Stem CellsSOXB1 Transcription FactorsZebrafishChromatinSox2 protein, mouseSOXB1 Transcription FactorsChIA-PETchromatin connectivityneural stem cellsSOX2transcription factors

Identifiers

PMID30849367
PMCPMC6506828
OpenAlexW2920879405

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.