Evidence map›Paper›PMID 40661394›Full record

ArticlebioRxiv : the preprint server for biology2025

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 readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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, United States.
Jenniluyn T NguyenWhitehead Institute, Cambridge, MA, United States.
Natalie G PfaltzgraffReproductive Sciences Center, Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Shelbie M WennerReproductive Sciences Center, Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.ORCID 0000-0002-7103-9928
Matthew KofronDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH United States.
Maria M MikedisReproductive Sciences Center, Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.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
NICHD NIH HHS K99 HD097285NICHD NIH HHS R00 HD097285
6 · The paper itself

Abstract

In multicellular organisms, germ cells' transformation into haploid gametes requires that they transition from mitosis to meiosis, whereby they stop mitotic cycling and enter the meiotic cell cycle. In mammals, transcriptional activator STRA8-MEIOSIN mediates the decision to enter the meiotic cell cycle by triggering the G1-to-meiotic S phase transition. However, the molecular basis by which mammalian germ cells prevent continued mitotic cycling before entering the meiotic cell cycle remains unclear. Here, we investigate MEIOC's role in the mitosis-to-meiosis transition during mouse oogenesis by analyzing proliferation, cell cycle transcriptomics, and cell cycle-associated protein expression. MEIOC was previously shown to destabilize mRNA and repress the mitotic program after meiotic entry. Here, we demonstrate that MEIOC prevents continued mitotic cycling prior to meiotic entry in oogenic cells. We find that the mitosis-to-meiosis transition involves the repression of G1/S cyclin CCNA2 at the transcript and protein levels, and that MEIOC downregulates CCNA2 protein expression. In addition, MEIOC promotes entry into meiotic S phase by increasing

Indexed as

fetal oocytesMEIOCMEIOSINmeiosisovarian germ cellSTRA8YTHDC2

Identifiers

PMID40661394
PMCPMC12258517

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.