Evidence map›Paper›PMID 32053104›Full record

ArticleeLife2020

Mechanisms of chromosome biorientation and bipolar spindle assembly analyzed by computational modeling.

Christopher Edelmaier, Adam R Lamson, Zachary R Gergely, Saad Ansari, Robert Blackwell, J Richard McIntosh, Matthew A Glaser, Meredith D Betterton

Abstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. The kinetochore corona orchestrates chromosome congression through transient microtubule interactions.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Measuring and modeling the dynamics of mitotic error correction.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Article
  13. Distinct regions of the kinesin-5 C-terminal tail are essential for mitotic spindle midzone localization and sliding force.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

8 authors.

Christopher EdelmaierDepartment of Physics, University of Colorado Boulder, Boulder, United States.ORCID 0000-0002-3673-1310
Adam R LamsonDepartment of Physics, University of Colorado Boulder, Boulder, United States.
Zachary R GergelyDepartment of Physics, University of Colorado Boulder, Boulder, United States.
Saad AnsariDepartment of Physics, University of Colorado Boulder, Boulder, United States.
Robert BlackwellDepartment of Physics, University of Colorado Boulder, Boulder, United States.
J Richard McIntoshDepartment of Molecular, Cellular, and Developmental Biology, University of Colorado Boulder, Boulder, United States.
Matthew A GlaserDepartment of Physics, University of Colorado Boulder, Boulder, United States.
Meredith D BettertonDepartment of Physics, University of Colorado Boulder, Boulder, United States.ORCID 0000-0002-5430-5518

Funding

Mechanisms of Kinesin-5 Motors in Mitotic Spindle AssemblyR01GM124371 · NIGMS · UNIVERSITY OF COLORADO · PI BETTERTON, MEREDITH · 2018 to 2021
$1.3M
Assessing the Contributions of Microtubule Dynamic Instability and Microtubule RoK25GM110486 · NIGMS · UNIVERSITY OF COLORADO · PI BETTERTON, MEREDITH · 2014 to 2016
$439k
National Science Foundation ACI-153223National Science Foundation ACI153223National Science Foundation ACI-1532235National Science Foundation ACI1532235National Science Foundation DMR-1420736National Science Foundation DMR1420736National Science Foundation DMR-1725065National Science Foundation DMR1725065National Science Foundation DMS-1620003National Science Foundation DMS1620003NIGMS NIH HHS K25 GM110486NIGMS NIH HHS R01 GM124371NIH HHS R01GM124371
6 · The paper itself

Abstract

The essential functions required for mitotic spindle assembly and chromosome biorientation and segregation are not fully understood, despite extensive study. To illuminate the combinations of ingredients most important to align and segregate chromosomes and simultaneously assemble a bipolar spindle, we developed a computational model of fission-yeast mitosis. Robust chromosome biorientation requires progressive restriction of attachment geometry, destabilization of misaligned attachments, and attachment force dependence. Large spindle length fluctuations can occur when the kinetochore-microtubule attachment lifetime is long. The primary spindle force generators are kinesin-5 motors and crosslinkers in early mitosis, while interkinetochore stretch becomes important after biorientation. The same mechanisms that contribute to persistent biorientation lead to segregation of chromosomes to the poles after anaphase onset. This model therefore provides a framework to interrogate key requirements for robust chromosome biorientation, spindle length regulation, and force generation in the spindle.

Indexed as

Chromosome SegregationComputer SimulationSpindle ApparatusKinetochoresMitosisModels, Biologicalcell biologycomputationcomputational biologycytoskeletonmitosisspindleS. pombesystems biologysystems modeling

Identifiers

PMID32053104
PMCPMC7311174

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.