Evidence map›Paper›PMID 35102267›Full record

ArticleNature cell biology2022

A monoastral mitotic spindle determines lineage fate and position in the mouse embryo.

Oz Pomp, Hui Yi Grace Lim, Robin M Skory, Adam A Moverley, Piotr Tetlak, Stephanie Bissiere, Nicolas Plachta

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Nature cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.3field-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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
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  5. Article
  6. Review
  7. Review
  8. Osmotic Pressure and Its Biological Implications.International journal of molecular sciences · 2024
    Review
  9. Article
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  11. Review
  12. Article
  13. Protein phase separation: new insights into cell division.Acta biochimica et biophysica Sinica · 2023
    Article
  14. Article
  15. Review
  16. Review
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 2 institutions in 2 countries.

Oz PompDepartment of Cell and Developmental Biology, Institute for Regenerative Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Hui Yi Grace LimInstitute of Molecular and Cell Biology, ASTAR, Singapore, Singapore.
Robin M SkoryDepartment of Cell and Developmental Biology, Institute for Regenerative Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Adam A MoverleyDepartment of Cell and Developmental Biology, Institute for Regenerative Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Piotr TetlakDepartment of Cell and Developmental Biology, Institute for Regenerative Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Stephanie BissiereDepartment of Cell and Developmental Biology, Institute for Regenerative Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Nicolas PlachtaDepartment of Cell and Developmental Biology, Institute for Regenerative Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. nicolas.plachta@pennmedicine.upenn.edu.ORCID http://orcid.org/0000-0002-5035-7425
California Institute for Regenerative Medicine · USAgency for Science, Technology and Research · SG

Funding

Revealing how cytoskeletal dynamics form the early mammalian embryoR01HD102013 · NICHD · UNIVERSITY OF PENNSYLVANIA · PI PLACHTA, NICOLAS · 2021 to 2025
$2.5M
Revealing how the mitotic spindle controls asymmetric cell division in vivoR01GM139970 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI PLACHTA, NICOLAS DANIEL · 2020 to 2023
$1.8M
NICHD NIH HHS R01 HD102013NIGMS NIH HHS R01 GM139970
6 · The paper itself

Abstract

During mammalian development, the first asymmetric cell divisions segregate cells into inner and outer positions of the embryo to establish the pluripotent and trophectoderm lineages. Typically, polarity components differentially regulate the mitotic spindle via astral microtubule arrays to trigger asymmetric division patterns. However, early mouse embryos lack centrosomes, the microtubule-organizing centres (MTOCs) that usually generate microtubule asters. Thus, it remains unknown whether spindle organization regulates lineage segregation. Here we find that heterogeneities in cell polarity in the early 8-cell-stage mouse embryo trigger the assembly of a highly asymmetric spindle organization. This spindle arises in an unusual modular manner, forming a single microtubule aster from an apically localized, non-centrosomal MTOC, before joining it to the rest of the spindle apparatus. When fully assembled, this 'monoastral' spindle triggers spatially asymmetric division patterns to segregate cells into inner and outer positions. Moreover, the asymmetric inheritance of spindle components causes differential cell polarization to determine pluripotent versus trophectoderm lineage fate.

Indexed as

Cell DifferentiationCell DivisionCell LineageCell PolarityAnimalsCell Cycle ProteinsEmbryo, MammalianEmbryonic DevelopmentGene Expression Regulation, DevelopmentalGestational AgeMiceMicrotubule-Associated ProteinsSpindle ApparatusCell Cycle ProteinsMicrotubule-Associated Proteins

Identifiers

PMID35102267
PMCPMC12272045
OpenAlexW4210772277

What OpenQuestion holds

Textmetadata
LicenceTDM
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.