Evidence map›Paper›PMID 29642041›Full record

ArticleBiophysical journal2018

Mechanical Model of Nuclei Ordering in Drosophila Embryos Reveals Dilution of Stochastic Forces.

Franz Kaiser, Zhiyi Lv, Daniel Marques Rodrigues, Jan Rosenbaum, Timo Aspelmeier, Jörg Großhans, Karen Alim

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Nuclear movement in multinucleated cells.Development (Cambridge, England) · 2022
    Review
  6. Article
  7. Review
  8. Article
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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

7 authors at 3 institutions in 1 country.

Franz KaiserBiological Physics and Morphogenesis Group, Max Planck Institute for Dynamics and Self-Organization, Göttingen, Germany.
Zhiyi LvInstitute for Developmental Biochemistry, Medical School, University of Göttingen, Göttingen, Germany.
Daniel Marques RodriguesInstitute for Developmental Biochemistry, Medical School, University of Göttingen, Göttingen, Germany.
Jan RosenbaumInstitute for Mathematical Stochastics and Felix-Bernstein-Institute for Mathematical Statistics in the Biosciences, University of Göttingen, Göttingen, Germany.
Timo AspelmeierInstitute for Mathematical Stochastics and Felix-Bernstein-Institute for Mathematical Statistics in the Biosciences, University of Göttingen, Göttingen, Germany.
Jörg GroßhansInstitute for Developmental Biochemistry, Medical School, University of Göttingen, Göttingen, Germany.
Karen AlimBiological Physics and Morphogenesis Group, Max Planck Institute for Dynamics and Self-Organization, Göttingen, Germany. Electronic address: karen.alim@ds.mpg.de.
University of Göttingen · DEBernstein Center for Computational Neuroscience Göttingen · DEMax Planck Institute for Dynamics and Self-Organization · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the initial development of syncytial embryos, nuclei go through cycles of nuclear division and spatial rearrangement. The arising spatial pattern of nuclei is important for subsequent cellularization and morphing of the embryo. Although nuclei are contained within a common cytoplasm, cytoskeletal proteins are nonuniformly packaged into regions around every nucleus. In fact, cytoskeletal elements like microtubules and their associated motor proteins exert stochastic forces between nuclei, actively driving their rearrangement. Yet, it is unknown how the stochastic forces are balanced to maintain nuclear order in light of increased nuclear density upon every round of divisions. Here, we investigate the nuclear arrangements in Drosophila melanogaster over the course of several nuclear divisions starting from interphase 11. We develop a theoretical model in which we distinguish long-ranged passive forces due to the nuclei as inclusions in the elastic matrix, namely the cytoplasm, and active, stochastic forces arising from the cytoskeletal dynamics mediated by motor proteins. We perform computer simulations and quantify the observed degree of orientational and spatial order of nuclei. Solely doubling the nuclear density upon nuclear division, the model predicts a decrease in nuclear order. Comparing results to experimental recordings of tracked nuclei, we make contradictory observations, finding an increase in nuclear order upon nuclear divisions. Our analysis of model parameters resulting from this comparison suggests that overall motor protein density as well as relative active-force amplitude has to decrease by a factor of about two upon nuclear division to match experimental observations. We therefore expect a dilution of cytoskeletal motors during the rapid nuclear division to account for the increase in nuclear order during syncytial embryo development. Experimental measurements of kinesin-5 cluster lifetimes support this theoretical finding.

Indexed as

Mechanical PhenomenaAnimalsBiomechanical PhenomenaCell NucleusDrosophila melanogasterEmbryo, NonmammalianMicrotubulesStochastic Processes

Identifiers

PMID29642041
PMCPMC5954298
OpenAlexW2796959620

What OpenQuestion holds

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Registered trials

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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.