Evidence map›Paper›PMID 35794113›Full record

ArticleNature communications2022

Nuclear speed and cycle length co-vary with local density during syncytial blastoderm formation in a cricket.

Seth Donoughe, Jordan Hoffmann, Taro Nakamura, Chris H Rycroft, Cassandra G Extavour

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Progressive Cellularization of Blastoderm and Extraembryonic Tissue Formation in the Ant Camponotus floridanus.Journal of experimental zoology. Part B, Molecular and developmental evolution · 2026
    Article
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  9. Origin and development of primary animal epithelia.BioEssays : news and reviews in molecular, cellular and developmental biology · 2024
    Review
  10. Germline and Somatic Cell Syncytia in Insects.Results and problems in cell differentiation · 2024
    Review
  11. Collective effects of cell cleavage dynamics.Frontiers in cell and developmental biology · 2024
    Review
  12. Enucleation of theLife science alliance · 2024
    Article
  13. Review
  14. Cell cycle control during early embryogenesis.Development (Cambridge, England) · 2021
    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

5 authors at 2 institutions in 2 countries.

Seth DonougheDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, USA. donoughe@uchicago.edu.ORCID 0000-0002-4773-5739
Jordan HoffmannJohn A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
Taro NakamuraDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, USA.ORCID 0000-0001-8341-3115
Chris H RycroftJohn A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA. chr@math.wisc.edu.ORCID 0000-0003-4677-6990
Cassandra G ExtavourDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, USA. extavour@oeb.harvard.edu.ORCID 0000-0003-2922-5855
Harvard University · USHoward Hughes Medical Institute · US

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

The blastoderm is a broadly conserved stage of early animal development, wherein cells form a layer at the embryo's periphery. The cellular behaviors underlying blastoderm formation are varied and poorly understood. In most insects, the pre-blastoderm embryo is a syncytium: nuclei divide and move throughout the shared cytoplasm, ultimately reaching the cortex. In Drosophila melanogaster, some early nuclear movements result from pulsed cytoplasmic flows that are coupled to synchronous divisions. Here, we show that the cricket Gryllus bimaculatus has a different solution to the problem of creating a blastoderm. We quantified nuclear dynamics during blastoderm formation in G. bimaculatus embryos, finding that: (1) cytoplasmic flows are unimportant for nuclear movement, and (2) division cycles, nuclear speeds, and the directions of nuclear movement are not synchronized, instead being heterogeneous in space and time. Moreover, nuclear divisions and movements co-vary with local nuclear density. We show that several previously proposed models for nuclear movements in D. melanogaster cannot explain the dynamics of G. bimaculatus nuclei. We introduce a geometric model based on asymmetric pulling forces on nuclei, which recapitulates the patterns of nuclear speeds and orientations of both unperturbed G. bimaculatus embryos, and of embryos physically manipulated to have atypical nuclear densities.

Indexed as

BlastodermGryllidaeAnimalsCell NucleusDrosophila melanogaster

Identifiers

PMID35794113
PMCPMC9259616
OpenAlexW4284881536

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.