Evidence map›Paper›PMID 29432416›Full record

ArticlePLoS genetics2018

SOX2 regulates common and specific stem cell features in the CNS and endoderm derived organs.

Daniel W Hagey, Susanne Klum, Idha Kurtsdotter, Cecile Zaouter, Danijal Topcic, Olov Andersson, Maria Bergsland, Jonas Muhr

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed, 64 citations in OpenAlex.

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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 1 institution in 1 country.

Daniel W HageyLudwig Institute for Cancer Research, Karolinska Institutet, Stockholm, Sweden.
Susanne KlumLudwig Institute for Cancer Research, Karolinska Institutet, Stockholm, Sweden.
Idha KurtsdotterLudwig Institute for Cancer Research, Karolinska Institutet, Stockholm, Sweden.
Cecile ZaouterLudwig Institute for Cancer Research, Karolinska Institutet, Stockholm, Sweden.
Danijal TopcicLudwig Institute for Cancer Research, Karolinska Institutet, Stockholm, Sweden.
Olov AnderssonDepartment of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden.
Maria BergslandLudwig Institute for Cancer Research, Karolinska Institutet, Stockholm, Sweden.
Jonas MuhrLudwig Institute for Cancer Research, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0003-0704-0788
Karolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stem cells are defined by their capacities to self-renew and generate progeny of multiple lineages. The transcription factor SOX2 has key roles in the regulation of stem cell characteristics, but whether SOX2 achieves these functions through similar mechanisms in distinct stem cell populations is not known. To address this question, we performed RNA-seq and SOX2 ChIP-seq on embryonic mouse cortex, spinal cord, stomach and lung/esophagus. We demonstrate that, although SOX2 binds a similar motif in the different cell types, its target regions are primarily cell-type-specific and enriched for the distinct binding motifs of appropriately expressed interacting co-factors. Furthermore, cell-type-specific SOX2 binding in endodermal and neural cells is most often found around genes specifically expressed in the corresponding tissue. Consistent with this, we demonstrate that SOX2 target regions can act as cis-regulatory modules capable of directing reporter expression to appropriate tissues in a zebrafish reporter assay. In contrast, SOX2 binding sites found in both endodermal and neural tissues are associated with genes regulating general stem cell features, such as proliferation. Notably, we provide evidence that SOX2 regulates proliferation through conserved mechanisms and target genes in both germ layers examined. Together, these findings demonstrate how SOX2 simultaneously regulates cell-type-specific, as well as core transcriptional programs in neural and endodermal stem cells.

Indexed as

AnimalsCell DifferentiationCell ProliferationCentral Nervous SystemEmbryo, NonmammalianEndodermGene Expression Regulation, DevelopmentalMiceMice, TransgenicMouse Embryonic Stem CellsNeural Stem CellsOrganogenesisPromoter Regions, GeneticProtein BindingSOXB1 Transcription FactorsSox2 protein, mouseSOXB1 Transcription Factors

Identifiers

PMID29432416
PMCPMC5825159
OpenAlexW2788070727

What OpenQuestion holds

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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.