Evidence map›Paper›PMID 34156079›Full record

ArticleBiology open2021

Altered germline cyst formation and oogenesis in Tex14 mutant mice.

Kanako Ikami, Nafisa Nuzhat, Haley Abbott, Ronald Pandoy, Lauren Haky, Allan C Spradling, Heather Tanner, Lei Lei

Open access · goldAbstract read
In one paragraph

Article in Biology open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Female Germline Cysts in Animals: Evolution and Function.Results and problems in cell differentiation · 2024
    Review
  11. Article
  12. Review
  13. Branched germline cysts and female-specific cyst fragmentation facilitate oocyte determination in mice.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  14. Article
  15. Review
  16. Review
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 at 3 institutions in 1 country.

Kanako IkamiBuck Institute for Research on Aging, 94949, Novato, CA, USA.
Nafisa NuzhatDepartment of Cell and Developmental Biology, University of Michigan Medical School, 48109, Ann Arbor, MI, USA.
Haley AbbottDepartment of Cell and Developmental Biology, University of Michigan Medical School, 48109, Ann Arbor, MI, USA.
Ronald PandoyBuck Institute for Research on Aging, 94949, Novato, CA, USA.
Lauren HakyBuck Institute for Research on Aging, 94949, Novato, CA, USA.
Allan C SpradlingDepartment of Embryology, Carnegie Institution for Science, 21218, Baltimore, MD, USA.
Heather TannerBuck Institute for Research on Aging, 94949, Novato, CA, USA.ORCID 0000-0002-5339-0044
Lei LeiBuck Institute for Research on Aging, 94949, Novato, CA, USA.ORCID 0000-0002-5594-5920
Buck Institute for Research on Aging · USUniversity of Michigan · USCarnegie Institution for Science · US

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
NIGMS NIH HHS R01 GM126028
6 · The paper itself

Abstract

During oocyte differentiation in mouse fetal ovaries, sister germ cells are connected by intercellular bridges, forming germline cysts. Within the cyst, primary oocytes form via gaining cytoplasm and organelles from sister germ cells through germ cell connectivity. To uncover the role of intercellular bridges in oocyte differentiation, we analyzed mutant female mice lacking testis-expressed 14 (TEX14), a protein involved in intercellular bridge formation and stabilization. In Tex14 homozygous mutant fetal ovaries, germ cells divide to form a reduced number of cysts in which germ cells remained connected via syncytia or fragmented cell membranes, rather than normal intercellular bridges. Compared with wild-type cysts, homozygous mutant cysts fragmented at a higher frequency and produced a greatly reduced number of primary oocytes with precocious cytoplasmic enrichment and enlarged volume. By contrast, Tex14 heterozygous mutant germline cysts were less fragmented and generate primary oocytes at a reduced size. Moreover, enlarged primary oocytes in homozygous mutants were used more efficiently to sustain folliculogenesis than undersized heterozygous mutant primary oocytes. Our observations directly link the nature of fetal germline cysts to oocyte differentiation and development.

Indexed as

MutationAnimalsCell DifferentiationCystsGene Expression Regulation, DevelopmentalGerm CellsHeterozygoteHomozygoteMiceOocytesOogenesisTranscription FactorsTEX14 protein, mouseTranscription FactorsGermline cystsOocytesOogenesisTEX14

Identifiers

PMID34156079
PMCPMC8249907
OpenAlexW3175806594

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.