Evidence map›Paper›PMID 25848744›Full record

ArticleeLife2015

The asymmetry of female meiosis reduces the frequency of inheritance of unpaired chromosomes.

Daniel B Cortes, Karen L McNally, Paul E Mains, Francis J McNally

Open access · goldAbstract read
In one paragraph

Article in eLife, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.2field-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

26 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. An egg sabotaging mechanism drives non-Mendelian transmission in mice.bioRxiv : the preprint server for biology · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Versatility of multivalent orientation, inverted meiosis, and rescued fitness in holocentric chromosomal hybrids.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  16. Multiple Aspects of PIP2 Involvement inInternational journal of molecular sciences · 2018
    Article
  17. Article
  18. Manipulation of Ploidy in Caenorhabditis elegans.Journal of visualized experiments : JoVE · 2018
    Article
  19. Article
  20. 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

4 authors at 2 institutions in 2 countries.

Daniel B CortesDepartment of Molecular and Cellular Biology, University of California, Davis, Davis, United States.
Karen L McNallyDepartment of Molecular and Cellular Biology, University of California, Davis, Davis, United States.
Paul E MainsDepartment of Biochemistry and Molecular Biology, University of Calgary, Calgary, Canada.
Francis J McNallyDepartment of Molecular and Cellular Biology, University of California, Davis, Davis, United States.
University of California, Davis · USUniversity of Calgary · CA

Funding

UC Davis MCB T32 Administrative Supplement to Recognize Excellence in Diversity, Equity, Inclusion, and Accessibility (DEIA) MentorshipT32GM007377 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI CHEDIN, FREDERIC LOUIS · 1985 to 2023
$9.9M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Mechanisms of asymmetric cell division during female meiosis.R01GM079421 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI MCNALLY, FRANCIS J · 2007 to 2019
$3.8M
NIGMS NIH HHS R01 GM079421NIGMS NIH HHS T32 GM007377NIH HHS P40 OD010440
6 · The paper itself

Abstract

Trisomy, the presence of a third copy of one chromosome, is deleterious and results in inviable or defective progeny if passed through the germ line. Random segregation of an extra chromosome is predicted to result in a high frequency of trisomic offspring from a trisomic parent. Caenorhabditis elegans with trisomy of the X chromosome, however, have far fewer trisomic offspring than expected. We found that the extra X chromosome was preferentially eliminated during anaphase I of female meiosis. We utilized a mutant with a specific defect in pairing of the X chromosome as a model to investigate the apparent bias against univalent inheritance. First, univalents lagged during anaphase I and their movement was biased toward the cortex and future polar body. Second, late-lagging univalents were frequently captured by the ingressing polar body contractile ring. The asymmetry of female meiosis can thus partially correct pre-existing trisomy.

Indexed as

Inheritance PatternsTrisomyAnaphaseAnimalsAsymmetric Cell DivisionCaenorhabditis elegansChromosome SegregationFemaleOocytesX ChromosomeC. eleganscell biologychromosomesgenesmeiosispolar bodytrisomy

Identifiers

PMID25848744
PMCPMC4412107
OpenAlexW2061033061

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.