Evidence map›Paper›PMID 23739662›Full record

ArticleNature communications2013

Zscan4 restores the developmental potency of embryonic stem cells.

Tomokazu Amano, Tetsuya Hirata, Geppino Falco, Manuela Monti, Lioudmila V Sharova, Misa Amano, Sarah Sheer, Hien G Hoang, Yulan Piao, Carole A Stagg and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Nature communications, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
4.0field-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

70 citing papers in PubMed, 109 citations in OpenAlex.

  1. Article
  2. In thePNAS nexus · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Genes as Genome Stabilizers in Pluripotent Stem Cells.Advances in experimental medicine and biology · 2025
    Review
  8. Review
  9. Reprogramming Chromosome Ends by Functional Histone Acetylation.International journal of molecular sciences · 2024
    Article
  10. Article
  11. ZSCAN4-binding motif-TGCACAC is conserved and enriched in CA/TG microsatellites in both mouse and human genomes.DNA research : an international journal for rapid publication of reports on genes and genomes · 2024
    Article
  12. Review
  13. International journal of molecular sciences · 2023
    Article
  14. Article
  15. Article
  16. Review
  17. Identification ofGenes · 2022
    Article
  18. Article
  19. Article
  20. Article

10 more citing papers are in PubMed but not listed here.

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

13 authors at 3 institutions in 3 countries.

Tomokazu AmanoDevelopmental Genomics and Aging Section, Laboratory of Genetics, National Institute on Aging, NIH, Baltimore, Maryland 21224, USA.
Tetsuya Hirata
Geppino Falco
Manuela Monti
Lioudmila V Sharova
Misa Amano
Sarah Sheer
Hien G Hoang
Yulan Piao
Carole A Stagg
Kohei Yamamizu
Tomohiko Akiyama
Minoru S H Ko
National Institute on Aging · USNational Institutes of Health · USUniversity of Sannio · IT

Funding

Development and maintenance of bioinformatics tools for mouse biologyZIAAG000702 · NIA · NATIONAL INSTITUTE ON AGING · PI SCHLESSINGER, DAVID · 2009 to 2016
$4.1M
Cellular commitment to mortality: analyses of mouse early embryoZIAAG000655 · NIA · NATIONAL INSTITUTE ON AGING · PI SCHLESSINGER, DAVID · 2009 to 2013
$2.8M
Function of Zscan4 in ES cells and early embryosZIAAG000706 · NIA · NATIONAL INSTITUTE ON AGING · PI KO, MINORU · 2009 to 2011
$1.4M
Transcription factor-manipulable mouse ES cell bankZIAAG000700 · NIA · NATIONAL INSTITUTE ON AGING · PI KO, MINORU · 2009 to 2011
$1.3M
Intramural NIH HHS ZIA AG000655Intramural NIH HHS ZIA AG000700Intramural NIH HHS ZIA AG000702Intramural NIH HHS ZIA AG000706
6 · The paper itself

Abstract

The developmental potency of mouse embryonic stem (ES) cells, which is the ability to contribute to a whole embryo, is known to deteriorate during long-term cell culture. Previously, we have shown that ES cells oscillate between Zscan4(-) and Zscan4(+) states, and the transient activation of Zscan4 is required for the maintenance of telomeres and genome stability of ES cells. Here we show that increasing the frequency of Zscan4 activation in mouse ES cells restores and maintains their developmental potency in long-term cell culture. Injection of a single ES cell with such increased potency into a tetraploid blastocyst gives rise to an entire embryo with a higher success rate. These results not only provide a means to rejuvenate ES cells by manipulating Zscan4 expression, but also indicate the active roles of Zscan4 in the long-term maintenance of ES cell potency.

Indexed as

AnimalsCell LineEmbryonic Stem CellsFemaleMaleMiceMice, Inbred C57BLPolyploidyRecombinant Fusion ProteinsReproducibility of ResultsTelomereTranscription FactorsRecombinant Fusion ProteinsTranscription Factors

Identifiers

PMID23739662
PMCPMC3682791
OpenAlexW1984802615

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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.