Evidence map›Paper›PMID 39358443›Full record

ArticleCommunications biology2024

The mouse Balbiani body regulates primary oocyte quiescence via RNA storage.

Lei Lei, Kanako Ikami, Edgar Andres Diaz Miranda, Sooah Ko, Faith Wilson, Haley Abbott, Ronald Pandoy, Shiying Jin

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Building a resilient ovarian reserve: Early soma-oocyte interactions.Current topics in developmental biology · 2026
    Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. The dynamics of centromere assembly and disassembly during quiescence.bioRxiv : the preprint server for biology · 2025
    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

8 authors.

Lei LeiDepartment of Obstetrics, Gynecology and Women's Health, University of Missouri School of Medicine, Columbia, MO, 65211, USA. lln34@health.missouri.edu.ORCID 0000-0002-5594-5920
Kanako IkamiDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, 48109, USA.ORCID 0009-0008-6845-6078
Edgar Andres Diaz MirandaDepartment of Obstetrics, Gynecology and Women's Health, University of Missouri School of Medicine, Columbia, MO, 65211, USA.ORCID 0000-0001-6931-3767
Sooah KoDepartment of Obstetrics, Gynecology and Women's Health, University of Missouri School of Medicine, Columbia, MO, 65211, USA.
Faith WilsonDepartment of Obstetrics, Gynecology and Women's Health, University of Missouri School of Medicine, Columbia, MO, 65211, USA.
Haley AbbottDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, 48109, USA.
Ronald PandoyBuck Institute for Research on Aging, Novato, California, 94949, USA.ORCID 0000-0001-8184-7075
Shiying JinDepartment of Obstetrics, Gynecology and Women's Health, University of Missouri School of Medicine, Columbia, MO, 65211, USA.

Funding

Mouse oocyte fate determination via polarized cytoplasmic transport within germline cystsR01GM126028 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI LEI, LEI · 2019 to 2023
$1.8M
Epithelial stem cell regulation of pregnancy establishmentR56HD104821 · NICHD · UNIVERSITY OF MISSOURI-COLUMBIA · PI JIN, SHIYING · 2022 to 2022
$229k
NICHD NIH HHS R56 HD104821NIGMS NIH HHS R01 GM126028U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM126028
6 · The paper itself

Abstract

In mammalian females, the transition from dormancy in primordial follicles to follicular development is critical for maintaining ovarian function and reproductive longevity. In mice, the quiescent primary oocyte of the primordial follicle contains a Balbiani body (B-body), an organelle aggregate comprised of a spherical structure of Golgi complexes. Here we show that the structure of the B-body is maintained by microtubules and actin. The B-body stores mRNA-capping enzyme and 597 mRNAs associated with mRNA-decapping enzyme 1 A (DCP1A). Gene ontology analysis results indicate that proteins encoded by these mRNAs function in enzyme binding, cellular component organization and packing of telomere ends. Pharmacological depolymerization of microtubules or actin led to B-body disassociation and nascent protein synthesis around the dissociated B-bodies within three hours. An increased number of activated developing follicles were observed in ovaries with prolonged culture and the in vivo mouse model. Our results indicate that the mouse B-body is involved in the activation of dormant primordial follicles likely via translation of the B-body-associated RNAs in primary oocytes.

Indexed as

OocytesOvarian FollicleActinsAnimalsFemaleGolgi ApparatusMiceMicrotubulesRNARNA, MessengerActinsRNARNA, Messenger

Identifiers

PMID39358443
PMCPMC11447053

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.