Evidence map›Paper›PMID 23469192›Full record

ArticlePloS one2013

Dullard/Ctdnep1 modulates WNT signalling activity for the formation of primordial germ cells in the mouse embryo.

Satomi S Tanaka, Akihiro Nakane, Yasuka L Yamaguchi, Takeshi Terabayashi, Takaya Abe, Kazuki Nakao, Makoto Asashima, Kirsten A Steiner, Patrick P L Tam, Ryuichi Nishinakamura

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Current progress onFrontiers in cell and developmental biology · 2023
    Review
  8. Observational
  9. Article
  10. Mammalian primordial germ cell specification.Development (Cambridge, England) · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. BMP signaling and its modifiers in kidney development.Pediatric nephrology (Berlin, Germany) · 2014
    Review
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

10 authors at 4 institutions in 2 countries.

Satomi S TanakaDepartment of Kidney Development, Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, Japan.
Akihiro Nakane
Yasuka L Yamaguchi
Takeshi Terabayashi
Takaya Abe
Kazuki Nakao
Makoto Asashima
Kirsten A Steiner
Patrick P L Tam
Ryuichi Nishinakamura
Kumamoto University · JPChildren's Medical Research Institute · AUGenetic Resources Center · JPNational Institute of Advanced Industrial Science and Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dullard/Ctdnep1 is a member of the serine/threonine phosphatase family of the C-terminal domain of eukaryotic RNA polymerase II. Embryos lacking Dullard activity fail to form primordial germ cells (PGCs). In the mouse, the formation of PGCs is influenced by BMP4 and WNT3 activity. Although Dullard is reputed to negatively regulate BMP receptor function, in this study we found mutations in Dullard had no detectable effect on BMP4 and p-Smad activity. Furthermore Dullard mutations did not influence the dosage-dependent inductive effect of Bmp4 in PGC formation. However, Dullard may function as a positive regulator of WNT signalling. Combined loss of one copy each of Dullard and Wnt3 had a synergistic effect on the reduction of PGC numbers in the compound heterozygous embryo. In addition, loss of Dullard function was accompanied by down-regulation of WNT/β-catenin signalling activity and a reduction in the level of Dishevelled 2 (Dvl2). Therefore, Dullard may play a role in the fine-tuning of WNT signalling activity by modulating the expression of ligands/antagonists and the availability of Dvl2 protein during specification of the germ cell lineage.

Indexed as

Gene Expression Regulation, DevelopmentalAdaptor Proteins, Signal TransducingAnimalsbeta CateninBone Morphogenetic Protein 4Cell LineageDishevelled ProteinsEmbryo, MammalianGerm CellsHeterozygoteHomozygoteMiceMorphogenesisMutationPhosphoprotein PhosphatasesPhosphoproteinsAdaptor Proteins, Signal Transducingbeta CateninBmp4 protein, mouseBone Morphogenetic Protein 4Dishevelled ProteinsDullard protein, mouseDvl2 protein, mousePhosphoprotein PhosphatasesPhosphoproteinsSmad ProteinsWnt3 ProteinWnt3 protein, mouse

Identifiers

PMID23469192
PMCPMC3587611
OpenAlexW2020632841

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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.