Evidence map›Paper›PMID 25683802›Full record

ArticleCurrent biology : CB2015

Scaling, selection, and evolutionary dynamics of the mitotic spindle.

Reza Farhadifar, Charles F Baer, Aurore-Cécile Valfort, Erik C Andersen, Thomas Müller-Reichert, Marie Delattre, Daniel J Needleman

Abstract read
In one paragraph

Article in Current biology : CB, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing 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

61 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Polarization as a Process: The Potential of Process Ontology for Understanding Cellular Symmetry Breaking.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  5. Evolutionary cell biology comes of age.Journal of cell science · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Evolution of developmental bias explains divergent patterns of phenotypic evolution in two nematode clades.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Variation in mutational (co)variances.G3 (Bethesda, Md.) · 2023
    Article
  19. Regulation of organelle size and organization during development.Seminars in cell & developmental biology · 2023
    Review
  20. Phenotypic stasis with genetic divergence.Peer community journal · 2023
    Article

1 more citing papers are in PubMed but not listed here.

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

7 authors.

Reza FarhadifarSchool of Engineering and Applied Sciences, Department of Molecular and Cellular Biology, FAS Center for Systems Biology, Harvard University, Cambridge, MA 02138, USA. Electronic address: rfarhadifar@cgr.harvard.edu.
Charles F BaerDepartment of Biology and University of Florida Genetics Institute, University of Florida, Gainesville, FL 32611, USA.
Aurore-Cécile ValfortLaboratory of Molecular Biology of the Cell, UMR 5239, Ecole Normale Supérieure de Lyon, Centre National de la Recherche Scientifique, 69007 Lyon, France.
Erik C AndersenDepartment of Molecular Biosciences, Northwestern University, Evanston, IL 60208, USA.
Thomas Müller-ReichertExperimental Center, Faculty of Medicine Carl Gustav Carus, Technische Universität Dresden, Fiedlerstrasse 42, 01307 Dresden, Germany.
Marie DelattreLaboratory of Molecular Biology of the Cell, UMR 5239, Ecole Normale Supérieure de Lyon, Centre National de la Recherche Scientifique, 69007 Lyon, France.
Daniel J NeedlemanSchool of Engineering and Applied Sciences, Department of Molecular and Cellular Biology, FAS Center for Systems Biology, Harvard University, Cambridge, MA 02138, USA.

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Evolutionary Causes and Consequences of Variation in the Rate of MutationR01GM072639 · NIGMS · UNIVERSITY OF FLORIDA · PI BAER, CHARLES F · 2006 to 2010
$1.5M
Determination of the distribution of fitness effects of mutations in C. elegansR01GM107227 · NIGMS · UNIVERSITY OF FLORIDA · PI BAER, CHARLES F · 2014 to 2017
$1.1M
NIGMS NIH HHS R01 GM072639NIGMS NIH HHS R01GM072639NIGMS NIH HHS R01 GM107227NIH HHS P40 OD010440
6 · The paper itself

Abstract

backgroundCellular structures such as the nucleus, Golgi, centrioles, and spindle show remarkable diversity between species, but the mechanisms that produce these variations in cell biology are not known.

resultsHere we investigate the mechanisms that contribute to variations in morphology and dynamics of the mitotic spindle, which orchestrates chromosome segregation in all Eukaryotes and positions the division plane in many organisms. We use high-throughput imaging of the first division in nematodes to demonstrate that the measured effects of spontaneous mutations, combined with stabilizing selection on cell size, are sufficient to quantitatively explain both the levels of within-species variation in the spindle and its diversity over ∼100 million years of evolution. Furthermore, our finding of extensive within-species variation for the spindle demonstrates that there is not just one "wild-type" form, rather that cellular structures can exhibit a surprisingly broad diversity of naturally occurring behaviors.

conclusionsOur results argue that natural selection acts predominantly on cell size and indirectly influences the spindle through the scaling of the spindle with cell size. Previous studies have shown that the spindle also scales with cell size during early development. Thus, the scaling of the spindle with cell size controls its variation over both ontogeny and phylogeny.

Indexed as

Biological EvolutionAnimalsCaenorhabditisCaenorhabditis elegansCell DivisionCell SizeChromosome SegregationModels, BiologicalMutationSelection, GeneticSpecies SpecificitySpindle Apparatus

Identifiers

PMID25683802
PMCPMC10504684

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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.