Evidence map›Paper›PMID 27335123›Full record

ArticleMolecular biology of the cell2016

A novel chromosome segregation mechanism during female meiosis.

Karen Perry McNally, Michelle T Panzica, Taekyung Kim, Daniel B Cortes, Francis J McNally

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 47 citations in OpenAlex.

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  10. Acentrosomal spindle assembly and maintenance inMolecular biology of the cell · 2022
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  18. Review
  19. Understanding the Genetic Code.Journal of bacteriology · 2019
    Review
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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

5 authors at 2 institutions in 1 country.

Karen Perry McNallyDepartment of Molecular and Cellular Biology, University of California, Davis, Davis, CA 95616.
Michelle T PanzicaDepartment of Molecular and Cellular Biology, University of California, Davis, Davis, CA 95616.
Taekyung KimLudwig Institute for Cancer Research, San Diego, CA 92093 Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA 92093.
Daniel B CortesDepartment of Molecular and Cellular Biology, University of California, Davis, Davis, CA 95616.
Francis J McNallyDepartment of Molecular and Cellular Biology, University of California, Davis, Davis, CA 95616 fjmcnally@ucdavis.edu.
University of California, Davis · USUniversity of California San Diego · US

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

In a wide range of eukaryotes, chromosome segregation occurs through anaphase A, in which chromosomes move toward stationary spindle poles, anaphase B, in which chromosomes move at the same velocity as outwardly moving spindle poles, or both. In contrast, Caenorhabditis elegans female meiotic spindles initially shorten in the pole-to-pole axis such that spindle poles contact the outer kinetochore before the start of anaphase chromosome separation. Once the spindle pole-to-kinetochore contact has been made, the homologues of a 4-μm-long bivalent begin to separate. The spindle shortens an additional 0.5 μm until the chromosomes are embedded in the spindle poles. Chromosomes then separate at the same velocity as the spindle poles in an anaphase B-like movement. We conclude that the majority of meiotic chromosome movement is caused by shortening of the spindle to bring poles in contact with the chromosomes, followed by separation of chromosome-bound poles by outward sliding.

Indexed as

AnaphaseAnimalsCaenorhabditis elegansChromosome SegregationFemaleKinetochoresMeiosisMicrotubulesSpindle ApparatusSpindle Poles

Identifiers

PMID27335123
PMCPMC4985259
OpenAlexW2474287543

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.