Evidence map›Paper›PMID 25038041›Full record

ArticleDevelopment (Cambridge, England)2014

p120-catenin-dependent junctional recruitment of Shroom3 is required for apical constriction during lens pit morphogenesis.

Richard A Lang, Ken Herman, Albert B Reynolds, Jeffrey D Hildebrand, Timothy F Plageman

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

43 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
  2. Article
  3. Mapping Shroom3 expression across the adult mouse.Gene expression patterns : GEP · 2025
    Article
  4. Review
  5. Review
  6. CommonGenome research · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. The mechanical forces that shape our senses.Development (Cambridge, England) · 2022
    Review
  16. Article
  17. Review
  18. Assays for Apical Constriction Using the Xenopus Model.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  19. Article
  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

5 authors at 5 institutions in 1 country.

Richard A LangThe Visual System Group, Division of Pediatric Ophthalmology and Developmental Biology, Children's Hospital Research Foundation, University of Cincinnati, Cincinnati, OH 45229, USA.
Ken HermanCollege of Optometry, The Ohio State University, Columbus, OH 43210, USA.
Albert B ReynoldsDepartment of Cancer Biology, Vanderbilt University, Nashville, TN 37232, USA.
Jeffrey D HildebrandDepartment of Biological Sciences, University of Pittsburgh, Pittsburgh, PA 15260, USA.
Timothy F PlagemanCollege of Optometry, The Ohio State University, Columbus, OH 43210, USA plageman.3@osu.edu.
Cincinnati Children's Hospital Medical Center · USSUNY College of Optometry · USThe Ohio State University · USUniversity of Pittsburgh · USVanderbilt University · US

Funding

Wnt Pathway Regulation of Lens PolarityR01EY016241 · NEI · CINCINNATI CHILDRENS HOSP MED CTR · PI LANG, RICHARD A. · 2005 to 2014
$3.3M
Epithelial Cell Structure in Vertebrate DevelopmentR01GM067525 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HILDEBRAND, JEFFREY D · 2002 to 2010
$2.3M
Role of p120-catenin in cell transformationR01GM102524 · NIGMS · VANDERBILT UNIVERSITY · PI REYNOLDS, ALBERT B · 2013 to 2016
$1.2M
NEI NIH HHS R01 EY016241NIGMS NIH HHS 5R01 GM102524NIGMS NIH HHS R01 GM067525NIGMS NIH HHS R01 GM102524
6 · The paper itself

Abstract

Apical constriction (AC) is a widely utilized mechanism of cell shape change whereby epithelial cells transform from a cylindrical to conical shape, which can facilitate morphogenetic movements during embryonic development. Invertebrate epithelial cells undergoing AC depend on the contraction of apical cortex-spanning actomyosin filaments that generate force on the apical junctions and pull them toward the middle of the cell, effectively reducing the apical circumference. A current challenge is to determine whether these mechanisms are conserved in vertebrates and to identify the molecules responsible for linking apical junctions with the AC machinery. Utilizing the developing mouse eye as a model, we have uncovered evidence that lens placode AC may be partially dependent on apically positioned myosin-containing filaments associated with the zonula adherens. In addition we found that, among several junctional components, p120-catenin genetically interacts with Shroom3, a protein required for AC during embryonic morphogenesis. Further analysis revealed that, similar to Shroom3, p120-catenin is required for AC of lens cells. Finally, we determined that p120-catenin functions by recruiting Shroom3 to adherens junctions. Together, these data identify a novel role for p120-catenin during AC and further define the mechanisms required for vertebrate AC.

Indexed as

Gene Expression Regulation, DevelopmentalActomyosinAdherens JunctionsAnimalsCateninsCytoskeletonDelta CateninGene DeletionGenotypeLens, CrystallineMiceMice, TransgenicMicrofilament ProteinsMorphogenesisNonmuscle Myosin Type IIBTime FactorsActomyosinCateninsCtnnd1 protein, mouseDelta CateninMicrofilament ProteinsNonmuscle Myosin Type IIBShrm protein, mouseApical constrictiondelta1 catenin (Ctnnd1)InvaginationLens pit morphogenesisp120-cateninShroom3

Identifiers

PMID25038041
PMCPMC4197547
OpenAlexW2144414716

What OpenQuestion holds

Textmetadata
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.