Evidence map›Paper›PMID 26314899›Full record

ArticleScientific reports2015

Dissecting the role of distinct OCT4-SOX2 heterodimer configurations in pluripotency.

Natalia Tapia, Caitlin MacCarthy, Daniel Esch, Adele Gabriele Marthaler, Ulf Tiemann, Marcos J Araúzo-Bravo, Ralf Jauch, Vlad Cojocaru, Hans R Schöler

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

41 citing papers in PubMed, 71 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

9 authors at 4 institutions in 3 countries.

Natalia TapiaHeinrich Heine University, Faculty of Medicine, Moorenstraße 5, 40225 Düsseldorf, Germany.
Caitlin MacCarthyMax Planck Institute for Molecular Biomedicine, Department of Cell and Developmental Biology, Röntgentstraße, 20, Münster 48149, Germany.
Daniel EschMax Planck Institute for Molecular Biomedicine, Department of Cell and Developmental Biology, Röntgentstraße, 20, Münster 48149, Germany.
Adele Gabriele MarthalerMax Planck Institute for Molecular Biomedicine, Department of Cell and Developmental Biology, Röntgentstraße, 20, Münster 48149, Germany.
Ulf TiemannHeinrich Heine University, Faculty of Medicine, Moorenstraße 5, 40225 Düsseldorf, Germany.
Marcos J Araúzo-BravoGroup of Computational Biology and Systems Biomedicine, Biodonostia Health Research Institute, Doctor Begiristain s/n, 20014 San Sebastián, Spain.
Ralf JauchKey Laboratory of Regenerative Biology, South China Institute for Stem Cell Biology and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China.
Vlad CojocaruMax Planck Institute for Molecular Biomedicine, Department of Cell and Developmental Biology, Röntgentstraße, 20, Münster 48149, Germany.
Hans R SchölerMax Planck Institute for Molecular Biomedicine, Department of Cell and Developmental Biology, Röntgentstraße, 20, Münster 48149, Germany.
Max Planck Institute for Molecular Biomedicine · DEHeinrich Heine University Düsseldorf · DEGuangzhou Institutes of Biomedicine and Health · CNIkerbasque · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transcription factors OCT4 and SOX2 are required for generating induced pluripotent stem cells (iPSCs) and for maintaining embryonic stem cells (ESCs). OCT4 and SOX2 associate and bind to DNA in different configurations depending on the arrangement of their individual DNA binding elements. Here we have investigated the role of the different OCT4-SOX2-DNA assemblies in regulating and inducing pluripotency. To this end, we have generated SOX2 mutants that interfere with specific OCT4-SOX2 heterodimer configurations and assessed their ability to generate iPSCs and to rescue ESC self-renewal. Our results demonstrate that the OCT4-SOX2 configuration that dimerizes on a Hoxb1-like composite, a canonical element with juxtaposed individual binding sites, plays a more critical role in the induction and maintenance of pluripotency than any other OCT4-SOX2 configuration. Overall, the results of this study provide new insight into the protein interactions required to establish a de novo pluripotent network and to maintain a true pluripotent cell fate.

Indexed as

Protein MultimerizationAnimalsCell DifferentiationCellular ReprogrammingHuman Embryonic Stem CellsHumansMice, TransgenicModels, MolecularOctamer Transcription Factor-3Pluripotent Stem CellsSOXB1 Transcription FactorsOctamer Transcription Factor-3SOXB1 Transcription Factors

Identifiers

PMID26314899
PMCPMC4551974
OpenAlexW2129148890

What OpenQuestion holds

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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.