Evidence map›Paper›PMID 25912690›Full record

ArticleDevelopmental biology2015

Imprinted expression in cystic embryoid bodies shows an embryonic and not an extra-embryonic pattern.

Tomasz M Kulinski, M Rita T Casari, Philipp M Guenzl, Daniel Wenzel, Daniel Andergassen, Anastasiya Hladik, Paul Datlinger, Matthias Farlik, H-Christian Theussl, Josef M Penninger and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Developmental biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 7 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

14 authors at 5 institutions in 1 country.

Tomasz M KulinskiCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, AKH-BT25.3, 1090 Vienna, Austria. Electronic address: tkulinski@ibb.waw.pl.
M Rita T CasariCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, AKH-BT25.3, 1090 Vienna, Austria. Electronic address: rcasari@cemm.oeaw.ac.at.
Philipp M GuenzlCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, AKH-BT25.3, 1090 Vienna, Austria. Electronic address: pguenzl@cemm.oeaw.ac.at.
Daniel WenzelIMBA, Institute of Molecular Biotechnology of the Austrian Academy of Sciences, Dr. Bohr Gasse 3, 1030 Vienna, Austria. Electronic address: daniel.wenzel@imba.oeaw.ac.at.
Daniel AndergassenCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, AKH-BT25.3, 1090 Vienna, Austria. Electronic address: dandergassen@cemm.oeaw.ac.at.
Anastasiya HladikCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, AKH-BT25.3, 1090 Vienna, Austria; Department of Medicine 1, Laboratory of Infection Biology, Medical University of Vienna, 1090 Vienna, Austria. Electronic address: ahladik@cemm.oeaw.ac.at.
Paul DatlingerCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, AKH-BT25.3, 1090 Vienna, Austria. Electronic address: pdatlinger@cemm.oeaw.ac.at.
Matthias FarlikCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, AKH-BT25.3, 1090 Vienna, Austria. Electronic address: mfarlik@cemm.oeaw.ac.at.
H-Christian TheusslIMP/IMBA Transgenic Service, Institute of Molecular Pathology (IMP), Dr. Bohr Gasse 7, 1030 Vienna, Austria. Electronic address: christian.theussl@imp.ac.at.
Josef M PenningerIMBA, Institute of Molecular Biotechnology of the Austrian Academy of Sciences, Dr. Bohr Gasse 3, 1030 Vienna, Austria. Electronic address: josef.penninger@imba.oeaw.ac.at.
Sylvia KnappCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, AKH-BT25.3, 1090 Vienna, Austria; Department of Medicine 1, Laboratory of Infection Biology, Medical University of Vienna, 1090 Vienna, Austria. Electronic address: sknapp@cemm.oeaw.ac.at.
Christoph BockCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, AKH-BT25.3, 1090 Vienna, Austria. Electronic address: cbock@cemm.oeaw.ac.at.
Denise P BarlowCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, AKH-BT25.3, 1090 Vienna, Austria. Electronic address: dbarlow@cemm.oeaw.ac.at.
Quanah J HudsonCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, AKH-BT25.3, 1090 Vienna, Austria. Electronic address: qhudson@cemm.oeaw.ac.at.
Austrian Academy of Sciences · ATCeMM Research Center for Molecular Medicine · ATInstitute of Molecular Biotechnology · ATMedical University of Vienna · ATResearch Institute of Molecular Pathology · AT

Funding

Austrian Science Fund FWF P 25185
6 · The paper itself

Abstract

A large subset of mammalian imprinted genes show extra-embryonic lineage (EXEL) specific imprinted expression that is restricted to placental trophectoderm lineages and to visceral yolk sac endoderm (ysE). Isolated ysE provides a homogenous in vivo model of a mid-gestation extra-embryonic tissue to examine the mechanism of EXEL-specific imprinted gene silencing, but an in vitro model of ysE to facilitate more rapid and cost-effective experiments is not available. Reports indicate that ES cells differentiated into cystic embryoid bodies (EBs) contain ysE, so here we investigate if cystic EBs model ysE imprinted expression. The imprinted expression pattern of cystic EBs is shown to resemble fetal liver and not ysE. To investigate the reason for this we characterized the methylome and transcriptome of cystic EBs in comparison to fetal liver and ysE, by whole genome bisulphite sequencing and RNA-seq. Cystic EBs show a fetal liver pattern of global hypermethylation and low expression of repeats, while ysE shows global hypomethylation and high expression of IAPEz retroviral repeats, as reported for placenta. Transcriptome analysis confirmed that cystic EBs are more similar to fetal liver than ysE and express markers of early embryonic endoderm. Genome-wide analysis shows that ysE shares epigenetic and repeat expression features with placenta. Contrary to previous reports, we show that cystic EBs do not contain ysE, but are more similar to the embryonic endoderm of fetal liver. This explains why cystic EBs reproduce the imprinted expression seen in the embryo but not that seen in the ysE.

Indexed as

DNA MethylationModels, BiologicalAnimalsBase SequenceCell DifferentiationChromatin ImmunoprecipitationComputational BiologyEmbryoid BodiesEndodermGene Expression ProfilingGene Expression Regulation, DevelopmentalGenomic ImprintingHistological TechniquesIn Situ HybridizationMiceMolecular Sequence DataCystic embryoid bodies (EBs)DNA methylationGenomic imprintingVisceral endoderm (VE)Visceral yolk sac Endoderm (ysE)Visceral yolk sac (VYS)

Identifiers

PMID25912690
PMCPMC4454777
OpenAlexW1987395135

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Registered trials

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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.