Evidence map›Paper›PMID 34075040›Full record

ArticleNature communications2021

Meiosis-specific ZFP541 repressor complex promotes developmental progression of meiotic prophase towards completion during mouse spermatogenesis.

Yuki Horisawa-Takada, Chisato Kodera, Kazumasa Takemoto, Akihiko Sakashita, Kenichi Horisawa, Ryo Maeda, Ryuki Shimada, Shingo Usuki, Sayoko Fujimura, Naoki Tani and 10 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 36 citations in OpenAlex.

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  12. Epigenetic priming in the male germline.Current opinion in genetics & development · 2024
    Review
  13. Article
  14. Gene regulation during meiosis.Trends in genetics : TIG · 2024
    Review
  15. Article
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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

20 authors at 5 institutions in 2 countries.

Yuki Horisawa-TakadaDepartment of Chromosome Biology, Institute of Molecular Embryology and Genetics (IMEG), Kumamoto University, Kumamoto, Japan.ORCID 0000-0003-1083-997X
Chisato Kodera *Department of Chromosome Biology, Institute of Molecular Embryology and Genetics (IMEG), Kumamoto University, Kumamoto, Japan.
Kazumasa Takemoto *Department of Chromosome Biology, Institute of Molecular Embryology and Genetics (IMEG), Kumamoto University, Kumamoto, Japan.ORCID 0000-0003-3028-8685
Akihiko SakashitaDepartment of Molecular Biology, Keio University School of Medicine, Tokyo, Japan.
Kenichi HorisawaDivision of Organogenesis and Regeneration, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Ryo MaedaGraduate School of Frontier Biosciences, Osaka University, Osaka, Japan.
Ryuki ShimadaDepartment of Chromosome Biology, Institute of Molecular Embryology and Genetics (IMEG), Kumamoto University, Kumamoto, Japan.ORCID 0000-0001-6724-0875
Shingo UsukiLiaison Laboratory Research Promotion Center, IMEG, Kumamoto University, Kumamoto, Japan.
Sayoko FujimuraLiaison Laboratory Research Promotion Center, IMEG, Kumamoto University, Kumamoto, Japan.
Naoki TaniLiaison Laboratory Research Promotion Center, IMEG, Kumamoto University, Kumamoto, Japan.
Kumi MatsuuraDepartment of Pluripotent Stem Cell Biology, IMEG, Kumamoto University, Kumamoto, Japan.
Tomohiko AkiyamaDepartment of Systems Medicine, Keio University School of Medicine, Tokyo, Japan.
Atsushi SuzukiDivision of Organogenesis and Regeneration, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.ORCID 0000-0002-6347-5498
Hitoshi NiwaDepartment of Pluripotent Stem Cell Biology, IMEG, Kumamoto University, Kumamoto, Japan.
Makoto TachibanaGraduate School of Frontier Biosciences, Osaka University, Osaka, Japan.
Takashi OhbaDepartment of Obstetrics and Gynecology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Hidetaka KatabuchiDepartment of Obstetrics and Gynecology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Satoshi H NamekawaDepartment of Microbiology and Molecular Genetics, University of California, Davis, CA, USA.
Kimi ArakiInstitute of Resource Development and Analysis, and Center for Metabolic Regulation of Healthy Aging, Kumamoto University, Kumamoto, Japan.ORCID 0000-0002-1396-1527
Kei-Ichiro IshiguroDepartment of Chromosome Biology, Institute of Molecular Embryology and Genetics (IMEG), Kumamoto University, Kumamoto, Japan. ishiguro@kumamoto-u.ac.jp.ORCID 0000-0002-7515-1511
Kumamoto University · JPKeio University · JPKyushu University · JPUbe Frontier University · JPUniversity of California, Davis · US

Funding

Epigenetic Regulation of Gene Expression during SpermatogenesisR01GM122776 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI NAMEKAWA, SATOSHI · 2018 to 2021
$1.4M
NIGMS NIH HHS R01 GM122776
6 · The paper itself

Abstract

During spermatogenesis, meiosis is accompanied by a robust alteration in gene expression and chromatin status. However, it remains elusive how the meiotic transcriptional program is established to ensure completion of meiotic prophase. Here, we identify a protein complex that consists of germ-cell-specific zinc-finger protein ZFP541 and its interactor KCTD19 as the key transcriptional regulators in mouse meiotic prophase progression. Our genetic study shows that ZFP541 and KCTD19 are co-expressed from pachytene onward and play an essential role in the completion of the meiotic prophase program in the testis. Furthermore, our ChIP-seq and transcriptome analyses identify that ZFP541 binds to and suppresses a broad range of genes whose function is associated with biological processes of transcriptional regulation and covalent chromatin modification. The present study demonstrates that a germ-cell specific complex that contains ZFP541 and KCTD19 promotes the progression of meiotic prophase towards completion in male mice, and triggers the reconstruction of the transcriptional network and chromatin organization leading to post-meiotic development.

Indexed as

AnimalsCell Cycle ProteinsChromatin Immunoprecipitation SequencingChromosomal Proteins, Non-HistoneDisease Models, AnimalFemaleHistone Deacetylase 1Histone Deacetylase 2HumansInfertility, MaleMaleMiceMice, KnockoutNuclear ProteinsOocytesPachytene StageCell Cycle ProteinsChromosomal Proteins, Non-HistoneHdac1 protein, mouseHdac2 protein, mouseHistone Deacetylase 1Histone Deacetylase 2Kctd19 protein, mouseNuclear ProteinsPotassium Channels, Voltage-GatedTranscription FactorsZFP541 protein, mouse

Identifiers

PMID34075040
PMCPMC8169937
OpenAlexW3165228199

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.