Evidence map›Paper›PMID 32092049›Full record

ArticlePLoS genetics2020

Sycp2 is essential for synaptonemal complex assembly, early meiotic recombination and homologous pairing in zebrafish spermatocytes.

Kazumasa Takemoto, Yukiko Imai, Kenji Saito, Toshihiro Kawasaki, Peter M Carlton, Kei-Ichiro Ishiguro, Noriyoshi Sakai

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
7.9field-weighted citation impact, top 3% 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

38 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Article
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  4. The DNA mismatch repair protein Msh4 is essential for meiosis of male but not for female in zebrafish.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2026
    Article
  5. Exploration of Novel Markers in Tan Sheep Spermatogenesis.Animals : an open access journal from MDPI · 2026
    Article
  6. Meiotic Recombination in Teleosts.Advances in experimental medicine and biology · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. A novel loss-of-functionFrontiers in genetics · 2025
    Article
  17. Article
  18. Review
  19. Article
  20. 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

7 authors at 4 institutions in 1 country.

Kazumasa TakemotoDepartment of Genetics, School of Life Science, SOKENDAI (The Graduate University for Advanced Studies), Mishima, Japan.
Yukiko ImaiDepartment of Gene Function and Phenomics, National Institute of Genetics, Mishima, Japan.ORCID 0000-0002-4716-2563
Kenji SaitoDepartment of Gene Function and Phenomics, National Institute of Genetics, Mishima, Japan.
Toshihiro KawasakiDepartment of Genetics, School of Life Science, SOKENDAI (The Graduate University for Advanced Studies), Mishima, Japan.
Peter M CarltonRadiation Biology Center and Graduate School of Biostudies, Kyoto University, Kyoto, Japan.ORCID 0000-0002-5320-6024
Kei-Ichiro IshiguroDepartment of Chromosome Biology, Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, Japan.ORCID 0000-0002-7515-1511
Noriyoshi SakaiDepartment of Genetics, School of Life Science, SOKENDAI (The Graduate University for Advanced Studies), Mishima, Japan.ORCID 0000-0001-8403-8281
National Institute of Genetics · JPKumamoto University · JPKyoto University · JPThe Graduate University for Advanced Studies, SOKENDAI · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Meiotic recombination is essential for faithful segregation of homologous chromosomes during gametogenesis. The progression of recombination is associated with dynamic changes in meiotic chromatin structures. However, whether Sycp2, a key structural component of meiotic chromatin, is required for the initiation of meiotic recombination is still unclear in vertebrates. Here, we describe that Sycp2 is required for assembly of the synaptonemal complex and early meiotic events in zebrafish spermatocytes. Our genetic screening by N-ethyl-N-nitrosourea mutagenesis revealed that ietsugu (its), a mutant zebrafish line with an aberrant splice site in the sycp2 gene, showed a defect during meiotic prophase I. The its mutation appeared to be a hypomorphic mutation compared to sycp2 knockout mutations generated by TALEN mutagenesis. Taking advantage of these sycp2 hypomorphic and knockout mutant lines, we demonstrated that Sycp2 is required for the assembly of the synaptonemal complex that is initiated in the vicinity of telomeres in wild-type zebrafish spermatocytes. Accordingly, homologous pairing, the foci of the meiotic recombinases Dmc1/Rad51 and RPA, and γH2AX signals were largely diminished in sycp2 knockout spermatocytes. Taken together, our data indicate that Sycp2 plays a critical role in not only the assembly of the synaptonemal complex, but also early meiotic recombination and homologous pairing, in vertebrates.

Indexed as

Homologous RecombinationAnimalsAnimals, Genetically ModifiedCell Cycle ProteinsGene Knockout TechniquesMaleMutationNuclear ProteinsSpermatocytesSynaptonemal ComplexZebrafishZebrafish ProteinsCell Cycle ProteinsNuclear ProteinsSycp2 protein, zebrafishZebrafish Proteins

Identifiers

PMID32092049
PMCPMC7062287
OpenAlexW3007472818

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.