Evidence map›Paper›PMID 35982303›Full record

ArticleNature plants2022

Tethering of cellulose synthase to microtubules dampens mechano-induced cytoskeletal organization in Arabidopsis pavement cells.

René Schneider, David W Ehrhardt, Elliot M Meyerowitz, Arun Sampathkumar

Open access · hybridAbstract read
In one paragraph

Article in Nature plants, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
12.0field-weighted citation impact, top 1% 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

21 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
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  11. Structure and growth of plant cell walls.Nature reviews. Molecular cell biology · 2024
    Review
  12. Cell geometry regulates tissue fracture.Nature communications · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Microtubule nucleation complex behavior is critical for cortical array homogeneityProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  19. Mechanosensing, from forces to structures.Frontiers in plant science · 2022
    Review
  20. 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

4 authors at 4 institutions in 3 countries.

René SchneiderMax Planck Institute of Molecular Plant Physiology, Potsdam, Germany.
David W EhrhardtDepartment of Plant Biology, Carnegie Institution for Science, Stanford, CA, USA.
Elliot M MeyerowitzSainsbury Laboratory, University of Cambridge, Cambridge, UK.ORCID 0000-0003-4798-5153
Arun SampathkumarMax Planck Institute of Molecular Plant Physiology, Potsdam, Germany. sampathkumar@mpimp-golm.mpg.de.ORCID 0000-0003-1703-0137
California Institute of Technology · USCarnegie Institution for Science · USMax Planck Institute of Molecular Plant Physiology · DEUniversity of Potsdam · DE

Funding

Signaling in cell expansion and morphogenesisR01GM123259 · NIGMS · CARNEGIE INSTITUTION OF WASHINGTON, D.C. · PI DINNENY, JOSE R, EHRHARDT, DAVID W · 2017 to 2020
$1.9M
NIGMS NIH HHS R01 GM123259
6 · The paper itself

Abstract

Mechanical forces control development in plants and animals, acting as cues in pattern formation and as the driving force of morphogenesis. In mammalian cells, molecular assemblies residing at the interface of the cell membrane and the extracellular matrix play an important role in perceiving and transmitting external mechanical signals to trigger physiological responses. Similar processes occur in plants, but there is little understanding of the molecular mechanisms and their genetic basis. Here, we show that the number and movement directions of cellulose synthase complexes (CSCs) at the plasma membrane vary during initial stages of development in the cotyledon epidermis of Arabidopsis, closely mirroring the microtubule organization. Uncoupling microtubules and CSCs resulted in enhanced microtubule co-alignment as caused by mechanical stimuli driven either by cell shape or by tissue-scale physical perturbations. Furthermore, micromechanical perturbation resulted in depletion of CSCs from the plasma membrane, suggesting a possible link between cellulose synthase removal from the plasma membrane and microtubule response to mechanical stimuli. Taken together, our results suggest that the interaction of cellulose synthase with cortical microtubules forms a physical continuum between the cell wall, plasma membrane and the cytoskeleton that modulates the mechano-response of the cytoskeleton.

Indexed as

ArabidopsisArabidopsis ProteinsGlucosyltransferasesMicrotubulesArabidopsis Proteinscellulose synthaseGlucosyltransferases

Identifiers

PMID35982303
PMCPMC9477734
OpenAlexW4292327169

What OpenQuestion holds

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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.