Evidence map›Paper›PMID 27199373›Full record

ArticleJournal of cell science2016

Meiotic onset is reliant on spatial distribution but independent of germ cell number in the mouse ovary.

Ripla Arora, Emilie Abby, Adam D J Ross, Andrea V Cantu, Michael D Kissner, Vianca Castro, Hsin-Yi Henry Ho, Gabriel Livera, Diana J Laird

Open access · greenAbstract read
In one paragraph

Article in Journal of cell science, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Ovary Development: Insights From a Three-Dimensional Imaging Revolution.Frontiers in cell and developmental biology · 2021
    Review
  8. Article
  9. Two distinct pathways of pregranulosa cell differentiation support follicle formation in the mouse ovary.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  10. Article
  11. Article
  12. Heterogeneity of primordial germ cells.Current topics in developmental biology · 2019
    Review
  13. 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

9 authors at 3 institutions in 2 countries.

Ripla AroraDepartment of Ob/Gyn and Reproductive Sciences, Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California, San Francisco, 35 Medical Center Way, San Francisco, CA 94143, USA.
Emilie AbbyUniversity Paris Diderot, Sorbonne Paris Cite, Laboratory of Development of the Gonads; CEA, DSV, iRCM, SCSR, LDG; INSERM, Unit of Genetic Stability, Stem cells and Radiation, UMR-967; University Paris-Sud, Fontenay-aux-Roses F-92265, France.ORCID 0000-0003-0284-4760
Adam D J RossDepartment of Ob/Gyn and Reproductive Sciences, Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California, San Francisco, 35 Medical Center Way, San Francisco, CA 94143, USA.
Andrea V CantuDepartment of Ob/Gyn and Reproductive Sciences, Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California, San Francisco, 35 Medical Center Way, San Francisco, CA 94143, USA.
Michael D KissnerDepartment of Ob/Gyn and Reproductive Sciences, Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California, San Francisco, 35 Medical Center Way, San Francisco, CA 94143, USA.ORCID 0000-0001-7603-2402
Vianca CastroDepartment of Ob/Gyn and Reproductive Sciences, Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California, San Francisco, 35 Medical Center Way, San Francisco, CA 94143, USA.
Hsin-Yi Henry HoDepartment of Cell Biology and Human Anatomy, University of California, Davis School of Medicine, 4422 Tupper Hall, Davis, CA 95616, USA.
Gabriel LiveraUniversity Paris Diderot, Sorbonne Paris Cite, Laboratory of Development of the Gonads; CEA, DSV, iRCM, SCSR, LDG; INSERM, Unit of Genetic Stability, Stem cells and Radiation, UMR-967; University Paris-Sud, Fontenay-aux-Roses F-92265, France.
Diana J LairdDepartment of Ob/Gyn and Reproductive Sciences, Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California, San Francisco, 35 Medical Center Way, San Francisco, CA 94143, USA diana.laird@ucsf.edu.ORCID 0000-0002-4930-0560
Broad Center · USInserm · FRUniversity of California, Davis · US

Funding

PREDOCTORAL TRAINING IN DEVELOPMENTAL BIOLOGYT32HD007470 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Todd Nystul · 1994 to 2026
$7.7M
REPRODUCTIVE ENDOCRINOLOGYT32HD007263 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MELLON, SYNTHIA H · 1985 to 2023
$4.1M
Cell competition in the developing mouse germlineDP2OD007420 · OD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LAIRD, DIANA J · 2010 to 2014
$2.4M
Assessing transgenerational effects of Phthalates on primordial germ cellsR21ES023297 · NIEHS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LAIRD, DIANA J · 2013 to 2015
$944k
NICHD NIH HHS T32 HD007263NICHD NIH HHS T32 HD007470NIEHS NIH HHS R21 ES023297NIH HHS DP2 OD007420
6 · The paper itself

Abstract

Mouse ovarian germ cells enter meiosis in a wave that propagates from anterior to posterior, but little is known about contribution of germ cells to initiation or propagation of meiosis. In a Ror2 mutant with diminished germ cell number and migration, we find that overall timing of meiotic initiation is delayed at the population level. We use chemotherapeutic depletion to exclude a profoundly reduced number of germ cells as a cause for meiotic delay. We rule out sex reversal or failure to specify somatic support cells as contributors to the meiotic phenotype. Instead, we find that anomalies in the distribution of germ cells as well as gonad shape in mutants contribute to aberrant initiation of meiosis. Our analysis supports a model of meiotic initiation via diffusible signal(s), excludes a role for germ cells in commencing the meiotic wave and furnishes the first phenotypic demonstration of the wave of meiotic entry. Finally, our studies underscore the importance of considering germ cell migration defects while studying meiosis to discern secondary effects resulting from positioning versus primary meiotic entry phenotypes.

Indexed as

AnimalsCell CountCell MovementCell ShapeFemaleGerm CellsGonadsMeiosisMiceMutationOvaryReceptor Tyrosine Kinase-like Orphan ReceptorsSignal TransductionReceptor Tyrosine Kinase-like Orphan ReceptorsRor2 protein, mouseGerm cellGonadMeiosisMigrationRor2Wave

Identifiers

PMID27199373
PMCPMC5930833
OpenAlexW2397588214

What OpenQuestion holds

Textmetadata
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.