Evidence map›Paper›PMID 30383040›Full record

ArticlePLoS biology2018

Spatiotemporal coordination of cell division and growth during organ morphogenesis.

Samantha Fox, Paul Southam, Florent Pantin, Richard Kennaway, Sarah Robinson, Giulia Castorina, Yara E Sánchez-Corrales, Robert Sablowski, Jordi Chan, Verônica Grieneisen and 3 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
14.5field-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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 103 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Biregionally differentiated growth generates sharp apex and concave joints in leaves.The Plant journal : for cell and molecular biology · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Conserved physical mechanisms of cell and tissue elongation.Development (Cambridge, England) · 2024
    Review
  13. Article
  14. Developmental timing in plants.Nature communications · 2024
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 2 countries.

Samantha FoxDepartment of Cell and Developmental Biology, John Innes Centre, Norwich, England, United Kingdom.ORCID 0000-0003-1271-6412
Paul SouthamDepartment of Cell and Developmental Biology, John Innes Centre, Norwich, England, United Kingdom.
Florent PantinDepartment of Cell and Developmental Biology, John Innes Centre, Norwich, England, United Kingdom.
Richard KennawayDepartment of Cell and Developmental Biology, John Innes Centre, Norwich, England, United Kingdom.
Sarah RobinsonDepartment of Cell and Developmental Biology, John Innes Centre, Norwich, England, United Kingdom.
Giulia CastorinaDepartment of Cell and Developmental Biology, John Innes Centre, Norwich, England, United Kingdom.
Yara E Sánchez-CorralesDepartment of Cell and Developmental Biology, John Innes Centre, Norwich, England, United Kingdom.
Robert SablowskiDepartment of Cell and Developmental Biology, John Innes Centre, Norwich, England, United Kingdom.
Jordi ChanDepartment of Cell and Developmental Biology, John Innes Centre, Norwich, England, United Kingdom.
Verônica GrieneisenDepartment of Computational and Systems Biology, John Innes Centre, Norwich, England, United Kingdom.
Athanasius F M MaréeDepartment of Computational and Systems Biology, John Innes Centre, Norwich, England, United Kingdom.
J Andrew BanghamSchool of Computational Sciences, University of East Anglia, Norwich, England, United Kingdom.
Enrico CoenDepartment of Cell and Developmental Biology, John Innes Centre, Norwich, England, United Kingdom.
John Innes Centre · GBUniversity of East Anglia · GB

Funding

Biotechnology and Biological Sciences Research Council BB/F005555/1Biotechnology and Biological Sciences Research Council BB/F005997/1Biotechnology and Biological Sciences Research Council BB/J004588/1Biotechnology and Biological Sciences Research Council BB/L008920/1Biotechnology and Biological Sciences Research Council BB/M023117/1Biotechnology and Biological Sciences Research Council BB/P013511/1Biotechnology and Biological Sciences Research Council BBS/E/J/00000152Biotechnology and Biological Sciences Research Council BBS/E/J/00000594Biotechnology and Biological Sciences Research Council BBS/E/J/000C0645Biotechnology and Biological Sciences Research Council BBS/E/J/000C0646Biotechnology and Biological Sciences Research Council BBS/E/J/000PR9773Biotechnology and Biological Sciences Research Council BBS/E/J/000PR9788
6 · The paper itself

Abstract

A developing plant organ exhibits complex spatiotemporal patterns of growth, cell division, cell size, cell shape, and organ shape. Explaining these patterns presents a challenge because of their dynamics and cross-correlations, which can make it difficult to disentangle causes from effects. To address these problems, we used live imaging to determine the spatiotemporal patterns of leaf growth and division in different genetic and tissue contexts. In the simplifying background of the speechless (spch) mutant, which lacks stomatal lineages, the epidermal cell layer exhibits defined patterns of division, cell size, cell shape, and growth along the proximodistal and mediolateral axes. The patterns and correlations are distinctive from those observed in the connected subepidermal layer and also different from the epidermal layer of wild type. Through computational modelling we show that the results can be accounted for by a dual control model in which spatiotemporal control operates on both growth and cell division, with cross-connections between them. The interactions between resulting growth and division patterns lead to a dynamic distributions of cell sizes and shapes within a deforming leaf. By modulating parameters of the model, we illustrate how phenotypes with correlated changes in cell size, cell number, and organ size may be generated. The model thus provides an integrated view of growth and division that can act as a framework for further experimental study.

Indexed as

ArabidopsisArabidopsis ProteinsBasic Helix-Loop-Helix ProteinsCell DifferentiationCell DivisionCell ProliferationCell SizeGene Expression Regulation, PlantModels, BiologicalPlant DevelopmentPlant LeavesPlant StomataSpatio-Temporal AnalysisArabidopsis ProteinsBasic Helix-Loop-Helix ProteinsSPEECHLESS protein, Arabidopsis

Identifiers

PMID30383040
PMCPMC6211367
OpenAlexW2899180745

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.