Evidence map›Paper›PMID 25875616›Full record

ArticlePloS one2015

ChIP-Seq and RNA-Seq analyses identify components of the Wnt and Fgf signaling pathways as Prep1 target genes in mouse embryonic stem cells.

Audrey Laurent, Manuela Calabrese, Hans-Jörg Warnatz, Marie-Laure Yaspo, Vsevolod Tkachuk, Miguel Torres, Francesco Blasi, Dmitry Penkov

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.6field-weighted citation impact, top 6% 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

10 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
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 4 institutions in 4 countries.

Audrey LaurentIFOM (FIRC Institute of Molecular Oncology), IFOM-IEO-Campus, Milan, Italy.
Manuela CalabreseIFOM (FIRC Institute of Molecular Oncology), IFOM-IEO-Campus, Milan, Italy.
Hans-Jörg WarnatzDepartment of Vertebrate Genomics, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Marie-Laure YaspoDepartment of Vertebrate Genomics, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Vsevolod TkachukFaculty of Basic Medicine, Lomonosov Moscow State University, Moscow, Russia.
Miguel TorresDepartment of Cardiovascular Development and Repair, Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain.
Francesco BlasiIFOM (FIRC Institute of Molecular Oncology), IFOM-IEO-Campus, Milan, Italy.
Dmitry PenkovIFOM (FIRC Institute of Molecular Oncology), IFOM-IEO-Campus, Milan, Italy; Department of Experimental Cardiology, Russian Cardiology Research and Production Complex, Moscow, Russia.
FIRC Institute of Molecular Oncology · ITMax Planck Institute for Molecular Genetics · DEInstitute of Physiology and Basic Medicine · RUSpanish National Centre for Cardiovascular Research · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Prep1 (Pknox1) homeodomain transcription factor is essential at multiple stages of embryo development. In the E11.5 embryo trunk, we previously estimated that Prep1 binds about 3,300 genomic sites at a highly specific decameric consensus sequence, mainly governing basal cellular functions. We now show that in embryonic stem (ES) cells Prep1 binding pattern only partly overlaps that of the embryo trunk, with about 2,000 novel sites. Moreover, in ES cells Prep1 still binds mostly to promoters, as in total embryo trunk but, among the peaks bound exclusively in ES cells, the percentage of enhancers was three-fold higher. RNA-seq identifies about 1800 genes down-regulated in Prep1-/- ES cells which belong to gene ontology categories not enriched in the E11.5 Prep1i/i differentiated embryo, including in particular essential components of the Wnt and Fgf pathways. These data agree with aberrant Wnt and Fgf expression levels in the Prep1-/- ES cells with a deficient embryoid bodies (EBs) formation and differentiation. Re-establishment of the Prep1 level rescues the phenotype.

Indexed as

Mouse Embryonic Stem CellsAnimalsBinding SitesCell DifferentiationDNA-Binding ProteinsEmbryo, MammalianEmbryonic DevelopmentFibroblast Growth FactorsGene Expression Regulation, DevelopmentalGenomeHomeodomain ProteinsMiceWnt Signaling PathwayDNA-Binding ProteinsFibroblast Growth FactorsHomeodomain ProteinsPknox1 protein, mouse

Identifiers

PMID25875616
PMCPMC4395233
OpenAlexW1983026664

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.