Evidence map›Paper›PMID 37542070›Full record

ArticleCell death & disease2023

PRC1 suppresses a female gene regulatory network to ensure testicular differentiation.

So Maezawa, Masashi Yukawa, Kazuteru Hasegawa, Ryo Sugiyama, Mizuho Iizuka, Mengwen Hu, Akihiko Sakashita, Miguel Vidal, Haruhiko Koseki, Artem Barski and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

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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

12 authors at 4 institutions in 6 countries.

So MaezawaReproductive Sciences Center, Division of Developmental Biology, Perinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, 45229, USA. s-maezawa@rs.tus.ac.jp.
Masashi YukawaDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, 45229, USA.
Kazuteru HasegawaReproductive Sciences Center, Division of Developmental Biology, Perinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, 45229, USA.
Ryo SugiyamaDepartment of Applied Biological Science, Faculty of Science and Technology, Tokyo University of Science, Chiba, 278-8510, Japan.
Mizuho IizukaDepartment of Applied Biological Science, Faculty of Science and Technology, Tokyo University of Science, Chiba, 278-8510, Japan.
Mengwen HuReproductive Sciences Center, Division of Developmental Biology, Perinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, 45229, USA.ORCID 0000-0002-7480-6432
Akihiko SakashitaReproductive Sciences Center, Division of Developmental Biology, Perinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, 45229, USA.
Miguel VidalCentro de Investigaciones Biológicas Margarita Salas, Department of Cellular and Molecular Biology, Madrid, 28040, Spain.
Haruhiko KosekiDevelopmental Genetics Laboratory, RIKEN Center for Allergy and Immunology, Yokohama, Kanagawa, Japan.
Artem BarskiDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, 45229, USA.
Tony DeFalcoReproductive Sciences Center, Division of Developmental Biology, Perinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, 45229, USA.ORCID 0000-0003-4133-7040
Satoshi H NamekawaReproductive Sciences Center, Division of Developmental Biology, Perinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, 45229, USA. snamekawa@ucdavis.edu.ORCID 0000-0002-1052-943X
Cincinnati Children's Hospital Medical Center · USTokyo University of Science · JPCentro de Investigaciones Biológicas Margarita Salas · ESRIKEN Center for Integrative Medical Sciences · JP

Funding

Epigenetic gene regulations in the germlineR35GM141085 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Satoshi Namekawa · 2021 to 2026
$4.4M
DNA Damage Response Pathways in Meiotic Sex Chromosome InactivationR01GM098605 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI NAMEKAWA, SATOSHI · 2011 to 2020
$3.3M
Direct Epigenetic Reprogramming of T CellsDP2GM119134 · NIGMS · CINCINNATI CHILDRENS HOSP MED CTR · PI BARSKI, ARTEM · 2015 to 2015
$2.3M
Macrophage regulation of the spermatogonial stem cell nicheR35GM119458 · NIGMS · CINCINNATI CHILDRENS HOSP MED CTR · PI DEFALCO, TONY J. · 2016 to 2020
$1.9M
Exploring vascular-mesenchymal interactions in the stem cell nicheR01HD094698 · NICHD · CINCINNATI CHILDRENS HOSP MED CTR · PI DEFALCO, TONY J. · 2018 to 2022
$1.6M
Epigenetic Regulation of Gene Expression during SpermatogenesisR01GM122776 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI NAMEKAWA, SATOSHI · 2018 to 2021
$1.4M
NICHD NIH HHS R01 HD094698NIGMS NIH HHS DP2GM119134NIGMS NIH HHS R01GM098605NIGMS NIH HHS R01GM122776NIGMS NIH HHS R35 GM119458NIGMS NIH HHS R35GM119458NIGMS NIH HHS R35 GM141085NIGMS NIH HHS R35GM141085
6 · The paper itself

Abstract

Gonadal sex determination and differentiation are controlled by somatic support cells of testes (Sertoli cells) and ovaries (granulosa cells). In testes, the epigenetic mechanism that maintains chromatin states responsible for suppressing female sexual differentiation remains unclear. Here, we show that Polycomb repressive complex 1 (PRC1) suppresses a female gene regulatory network in postnatal Sertoli cells. We genetically disrupted PRC1 function in embryonic Sertoli cells after sex determination, and we found that PRC1-depleted postnatal Sertoli cells exhibited defective proliferation and cell death, leading to the degeneration of adult testes. In adult Sertoli cells, PRC1 suppressed specific genes required for granulosa cells, thereby inactivating the female gene regulatory network. Chromatin regions associated with female-specific genes were marked by Polycomb-mediated repressive modifications: PRC1-mediated H2AK119ub and PRC2-mediated H3K27me3. Taken together, this study identifies a critical Polycomb-based mechanism that suppresses ovarian differentiation and maintains Sertoli cell fate in adult testes.

Indexed as

HistonesPolycomb Repressive Complex 1Cell DifferentiationChromatinFemaleGene Regulatory NetworksHumansMalePolycomb-Group ProteinsPolycomb Repressive Complex 2TestisChromatinHistonesPolycomb-Group ProteinsPolycomb Repressive Complex 1Polycomb Repressive Complex 2

Identifiers

PMID37542070
PMCPMC10403552
OpenAlexW4385568325

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.