Evidence map›Paper›PMID 26578656›Full record

ArticleJournal of molecular cell biology2016

Spatial control of active CDC-42 during collective migration of hypodermal cells in Caenorhabditis elegans.

Marie-Hélène Ouellette, Emmanuel Martin, Germain Lacoste-Caron, Karim Hamiche, Sarah Jenna

Open access · bronzeAbstract read
In one paragraph

Article in Journal of molecular cell biology, 2016. 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
1.4field-weighted citation impact, top 20% 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, 24 citations in OpenAlex.

  1. Review
  2. The actin assembly regulatorbioRxiv : the preprint server for biology · 2025
    Article
  3. Functions of Arp2/3 Complex in the Dynamics of Epithelial Tissues.Frontiers in cell and developmental biology · 2022
    Review
  4. Article
  5. Epithelial morphogenesis, tubulogenesis and forces in organogenesis.Current topics in developmental biology · 2021
    Review
  6. Article
  7. Article
  8. Game of Tissues: How the Epidermis ThronesJournal of developmental biology · 2020
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Cdc42 regulates branching in angiogenic sprouting in vitro.Microcirculation (New York, N.Y. : 1994) · 2017
    Article
  16. Article
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 1 institution in 1 country.

Marie-Hélène OuelletteDepartment of Chemistry, Pharmaqam, Biomed, Université du Québec à Montréal, Montréal, Québec, Canada.
Emmanuel MartinDepartment of Chemistry, Pharmaqam, Biomed, Université du Québec à Montréal, Montréal, Québec, Canada.
Germain Lacoste-CaronDepartment of Chemistry, Pharmaqam, Biomed, Université du Québec à Montréal, Montréal, Québec, Canada.
Karim HamicheDepartment of Chemistry, Pharmaqam, Biomed, Université du Québec à Montréal, Montréal, Québec, Canada.
Sarah JennaDepartment of Chemistry, Pharmaqam, Biomed, Université du Québec à Montréal, Montréal, Québec, Canada jenna.sarah@uqam.ca.
Université du Québec à Montréal · CA

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
NIH HHS P40 OD010440
6 · The paper itself

Abstract

Collective epithelial cell migration requires the maintenance of cell-cell junctions while enabling the generation of actin-rich protrusions at the leading edge of migrating cells. Ventral enclosure of Caenorhabditis elegans embryos depends on the collective migration of anterior-positioned leading hypodermal cells towards the ventral midline where they form new junctions with their contralateral neighbours. In this study, we characterized the zygotic function of RGA-7/SPV-1, a CDC-42/Cdc42 and RHO-1/RhoA-specific Rho GTPase-activating protein, which controls the formation of actin-rich protrusions at the leading edge of leading hypodermal cells and the formation of new junctions between contralateral cells. We show that RGA-7 controls these processes in an antagonistic manner with the CDC-42's effector WSP-1/N-WASP and the CDC-42-binding proteins TOCA-1/2/TOCA1. RGA-7 is recruited to spatially distinct locations at junctions between adjacent leading cells, where it promotes the accumulation of clusters of activated CDC-42. It also inhibits the spreading of these clusters towards the leading edge of the junctions and regulates their accumulation and distribution at new junctions formed between contralateral leading cells. Our study suggests that RGA-7 controls collective migration and junction formation between epithelial cells by spatially restricting active CDC-42 within cell-cell junctions.

Indexed as

Cell MovementActinsAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell CompartmentationCell Cycle ProteinsCell Surface ExtensionsGreen Fluorescent ProteinsGTP-Binding ProteinsIntercellular JunctionsModels, BiologicalPseudopodiaSubcutaneous TissueActinsCaenorhabditis elegans Proteinscdc-42 protein, C elegansCell Cycle ProteinsGreen Fluorescent ProteinsGTP-Binding ProteinsCaenorhabditis elegansCdc42collective migrationepithelialmorphogenesisRho GAPventral enclosure

Identifiers

PMID26578656
PMCPMC4991665
OpenAlexW2269409612

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.