Evidence map›Paper›PMID 30728412›Full record

ArticleScientific reports2019

Robust and efficient knock-in in embryonic stem cells and early-stage embryos of the common marmoset using the CRISPR-Cas9 system.

Sho Yoshimatsu, Junko Okahara, Takefumi Sone, Yuta Takeda, Mari Nakamura, Erika Sasaki, Noriyuki Kishi, Seiji Shiozawa, Hideyuki Okano

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Non-human primate: the new frontier model of female reproductive engineering.Frontiers in bioengineering and biotechnology · 2025
    Review
  4. Marmosets as models of infectious diseases.Frontiers in cellular and infection microbiology · 2024
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. The dawn of non-human primate models for neurodevelopmental disorders.Current opinion in genetics & development · 2020
    Review
  16. Article
  17. Opportunities and limitations of genetically modified nonhuman primate models for neuroscience research.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Review
  18. Review
  19. Article
  20. 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

9 authors at 3 institutions in 1 country.

Sho YoshimatsuDepartment of Physiology, School of Medicine, Keio University, Shinjuku-ku, Tokyo, 160-8582, Japan.
Junko OkaharaLaboratory for Marmoset Neural Architecture, RIKEN Center for Brain Science, Wako City, Saitama, 351-0198, Japan.
Takefumi SoneDepartment of Physiology, School of Medicine, Keio University, Shinjuku-ku, Tokyo, 160-8582, Japan.ORCID 0000-0003-3467-679X
Yuta TakedaLaboratory for Marmoset Neural Architecture, RIKEN Center for Brain Science, Wako City, Saitama, 351-0198, Japan.
Mari NakamuraDepartment of Physiology, School of Medicine, Keio University, Shinjuku-ku, Tokyo, 160-8582, Japan.
Erika SasakiCentral Institute for Experimental Animals, Kawasaki, Kanagawa, 210-0821, Japan.
Noriyuki KishiLaboratory for Marmoset Neural Architecture, RIKEN Center for Brain Science, Wako City, Saitama, 351-0198, Japan.
Seiji ShiozawaDepartment of Physiology, School of Medicine, Keio University, Shinjuku-ku, Tokyo, 160-8582, Japan. shiozawa@a7.keio.jp.
Hideyuki OkanoDepartment of Physiology, School of Medicine, Keio University, Shinjuku-ku, Tokyo, 160-8582, Japan. hidokano@a2.keio.jp.
Keio University · JPCentral Institute for Experimental Animals · JPRIKEN Center for Brain Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome editing technology greatly facilitates the genetic modification of various cells and animals. The common marmoset (Callithrix jacchus), a small non-human primate which exhibits high reproductive efficiency, is a widely used animal model in biomedical research. Developing genome editing techniques in the common marmoset will further enhance its utility. Here, we report the successful establishment of a knock-in (KI) method for marmoset embryonic stem cells (ESCs), which is based on the CRISPR-Cas9 system. The use of CRISPR-Cas9, mediated by homologous recombination (HR), enhanced the KI efficiency in marmoset ESCs. Furthermore, we succeeded in performing KI in early-stage marmoset embryos. In the course of the experiments, we found that HR in the marmoset ESCs is innately highly efficient. This suggested that the marmoset possesses a repair mechanism for DNA double-strand breaks. The current study will facilitate the generation of genetically modified marmosets and gene function analysis in the marmoset.

Indexed as

CRISPR-Cas SystemsDNA Breaks, Double-StrandedGene EditingAnimalsCallithrixEmbryo, MammalianEmbryonic Stem CellsFemaleForkhead Transcription FactorsGene Knock-In TechniquesGene TargetingHomologous RecombinationHumansMaleModels, AnimalMyelin Proteolipid ProteinForkhead Transcription FactorsFOXP2 protein, humanMyelin Proteolipid Protein

Identifiers

PMID30728412
PMCPMC6365532
OpenAlexW2911472137

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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.