Evidence map›Paper›PMID 34812842›Full record

ArticleThe Journal of cell biology2022

Micron-scale supramolecular myosin arrays help mediate cytoskeletal assembly at mature adherens junctions.

Hui-Chia Yu-Kemp, Rachel A Szymanski, Daniel B Cortes, Nicole C Gadda, Madeline L Lillich, Amy S Maddox, Mark Peifer

Open access · greenAbstract read
In one paragraph

Article in The Journal of cell biology, 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
2.1field-weighted citation impact, top 14% 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, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Myosin 2 - A general contractor for the cytoskeleton.Current opinion in cell biology · 2025
    Review
  5. Structure, regulation, and mechanisms of nonmuscle myosin-2.Cellular and molecular life sciences : CMLS · 2024
    Review
  6. Article
  7. Too old for hide-and-seek; cell maturation reveals hidden apical junctional organization.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. 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 1 institution in 1 country.

Hui-Chia Yu-KempLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC.ORCID 0000-0002-4590-0892
Rachel A SzymanskiDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Daniel B CortesDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Nicole C GaddaDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC.ORCID 0000-0002-7493-8136
Madeline L LillichDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC.ORCID 0000-0002-5217-5393
Amy S MaddoxLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC.ORCID 0000-0002-4671-2949
Mark PeiferLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC.ORCID 0000-0003-1412-3987
University of North Carolina at Chapel Hill · US

Funding

Integrated Training in Cancer Model SystemsT32CA009156 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DER, CHANNING J. · 1985 to 2020
$19.7M
Regulating cell fate and shaping the body plan during morphogenesis and their alteration during oncogenesisR35GM118096 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Mark A. Peifer · 2016 to 2026
$6.5M
Super-resolution of the Mechanisms of Cell Shape Change in Cytokinesis - the Zeiss LSM800/AiryscanR01GM102390 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MADDOX, AMY SHAUB · 2012 to 2020
$2.9M
NCI NIH HHS T32 CA009156NIGMS NIH HHS R01 GM102390NIGMS NIH HHS R35 GM118096NIH HHS R01 GM102390NIH HHS R35 GM118096NIH HHS T32 CA009156
6 · The paper itself

Abstract

Epithelial cells assemble specialized actomyosin structures at E-Cadherin-based cell-cell junctions, and the force exerted drives cell shape change during morphogenesis. The mechanisms that build this supramolecular actomyosin structure remain unclear. We used ZO-knockdown MDCK cells, which assemble a robust, polarized, and highly organized actomyosin cytoskeleton at the zonula adherens, combining genetic and pharmacologic approaches with superresolution microscopy to define molecular machines required. To our surprise, inhibiting individual actin assembly pathways (Arp2/3, formins, or Ena/VASP) did not prevent or delay assembly of this polarized actomyosin structure. Instead, as junctions matured, micron-scale supramolecular myosin arrays assembled, with aligned stacks of myosin filaments adjacent to the apical membrane, overlying disorganized actin filaments. This suggested that myosin arrays might bundle actin at mature junctions. Consistent with this idea, inhibiting ROCK or myosin ATPase disrupted myosin localization/organization and prevented actin bundling and polarization. We obtained similar results in Caco-2 cells. These results suggest a novel role for myosin self-assembly, helping drive actin organization to facilitate cell shape change.

Indexed as

Actin CytoskeletonActin-Related Protein 2-3 ComplexActinsActomyosinAdherens JunctionsAnimalsCaco-2 CellsCytoskeletonDNA-Binding ProteinsDogsForminsHumansMadin Darby Canine Kidney CellsModels, BiologicalMyosin-Light-Chain KinaseMyosinsActin-Related Protein 2-3 ComplexActinsActomyosinDNA-Binding ProteinsENA-VASP proteinsForminsMyosin-Light-Chain KinaseMyosinsrho-Associated Kinases

Identifiers

PMID34812842
PMCPMC8614156
OpenAlexW3214749087

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.