Evidence map›Paper›PMID 41287933›Full record

ArticleDevelopment (Cambridge, England)2026

MEIOC prevents continued mitotic cycling and promotes meiotic entry during mouse oogenesis.

Esther G Ushuhuda, Jenniluyn T Nguyen, Natalie G Pfaltzgraff, Shelbie M Wenner, Matthew Kofron, Maria M Mikedis

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Esther G UshuhudaReproductive Sciences Center, Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Jenniluyn T NguyenWhitehead Institute, Cambridge, MA 02142, USA.
Natalie G PfaltzgraffReproductive Sciences Center, Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Shelbie M WennerReproductive Sciences Center, Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.ORCID 0000-0002-8951-9743
Matthew KofronDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA.
Maria M MikedisReproductive Sciences Center, Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.ORCID 0000-0001-7800-7120

Funding

Establishment of the meiotic cell cycle program through post-transcriptional regulation by MEIOC and YTHDC2R00HD097285 · NICHD · CINCINNATI CHILDRENS HOSP MED CTR · PI MIKEDIS, MARIA · 2022 to 2024
$727k
Establishment of the meiotic cell cycle program through post-transcriptional regulation by MEIOC and YTHDC2K99HD097285 · NICHD · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI MIKEDIS, MARIA · 2020 to 2022
$337k
National Institute of Child Health and Human DevelopmentNational Institute of Child Health and Human Development K99HD097285National Institute of Child Health and Human Development R00HD097285NIH HHS K99HD097285NIH HHS R00HD097285University of Cincinnati
6 · The paper itself

Abstract

To generate haploid gametes, germ cells must transition from mitosis to meiosis. In mammals, the transcriptional activator STRA8-MEIOSIN mediates the decision to enter the meiotic cell cycle, but how germ cells prevent continued mitotic cycling before meiotic entry remains unclear. MEIOC was previously shown to repress the mitotic program after meiotic entry. Here, we investigate the role of MEIOC in the mitosis-to-meiosis transition during mouse oogenesis. Using cell proliferation analysis and cell cycle transcriptomics, we demonstrate that MEIOC prevents continued mitotic cycling prior to meiotic entry in oogenic cells. We find that G1/S cyclin CCNA2 is downregulated during the mitosis-to-meiosis transition, and MEIOC contributes to this downregulation. MEIOC also promotes entry into meiosis by increasing Meiosin transcript abundance and consequently activating STRA8-MEIOSIN. Thus, in mouse oogenic cells, the transition from mitosis to meiosis occurs as two molecularly regulated steps - (1) the halt of mitotic cycling and (2) entry into the meiotic cell cycle - and that MEIOC modifies the cell cycle program to facilitate both steps in this transition.

Indexed as

MeiosisMitosisOogenesisAdaptor Proteins, Signal TransducingAnimalsCell ProliferationCyclin A2FemaleMiceAdaptor Proteins, Signal TransducingCCNA2 protein, mouseCyclin A2Stra8 protein, mouseFetal oocytesMEIOCMEIOSINMeiosisOvarian germ cellSTRA8

Identifiers

PMID41287933
PMCPMC12848572

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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.