Evidence map›Paper›PMID 29040749›Full record

ArticleJournal of molecular cell biology2018

Cdc42 regulates the cellular localization of Cdc42ep1 in controlling neural crest cell migration.

Shlomi Cohen, Daniel T Kovari, Wenbin Wei, Rebecca Keate, Jennifer E Curtis, Shuyi Nie

Open access · bronzeAbstract read
In one paragraph

Article in Journal of molecular cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Sex differences in human pre-gastrulation embryos.Science China. Life sciences · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
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  9. Article
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  11. Review
  12. MMP14 Regulates Cranial Neural Crest Epithelial-to-Mesenchymal Transition and Migration.Developmental dynamics : an official publication of the American Association of Anatomists · 2018
    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

6 authors at 2 institutions in 1 country.

Shlomi CohenSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA.
Daniel T KovariDepartment of Physics, Emory University, Atlanta, GA, USA.
Wenbin WeiSchool of Physics, Georgia Institute of Technology, Atlanta, GA, USA.
Rebecca KeateSchool of Physics, Georgia Institute of Technology, Atlanta, GA, USA.
Jennifer E CurtisSchool of Physics, Georgia Institute of Technology, Atlanta, GA, USA.
Shuyi NieSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA.
Georgia Institute of Technology · USEmory University · US

Funding

Coordinated Actin Regulation in Directed Neural Crest Cell MigrationR01GM136892 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI NIE, SHUYI · 2020 to 2024
$1.6M
Role of actin cytoskeleton regulators in craniofacial development and diseaseR00DE022796 · NIDCR · GEORGIA INSTITUTE OF TECHNOLOGY · PI NIE, SHUYI · 2014 to 2016
$758k
NIDCR NIH HHS R00 DE022796NIGMS NIH HHS R01 GM136892
6 · The paper itself

Abstract

The member of Rho family of small GTPases Cdc42 plays important and conserved roles in cell polarity and motility. The Cdc42ep family proteins have been identified to bind to Cdc42, yet how they interact with Cdc42 to regulate cell migration remains to be elucidated. In this study, we focus on Cdc42ep1, which is expressed predominantly in the highly migratory neural crest cells in frog embryos. Through morpholino-mediated knockdown, we show that Cdc42ep1 is required for the migration of cranial neural crest cells. Loss of Cdc42ep1 leads to rounder cell shapes and the formation of membrane blebs, consistent with the observed disruption in actin organization and focal adhesion alignment. As a result, Cdc42ep1 is critical for neural crest cells to apply traction forces at the correct place to migrate efficiently. We further show that Cdc42ep1 is localized to two areas in neural crest cells: in membrane protrusions together with Cdc42 and in perinuclear patches where Cdc42 is absent. Cdc42 directly interacts with Cdc42ep1 (through the CRIB domain) and changes in Cdc42 level shift the distribution of Cdc42ep1 between these two subcellular locations, controlling the formation of membrane protrusions and directionality of migration as a consequence. These results suggest that Cdc42ep1 elaborates Cdc42 activity in neural crest cells to promote their efficient migration.

Indexed as

Actin CytoskeletonAnimalsAnimals, Genetically ModifiedCartilageCell MovementCytoskeletal ProteinsEmbryo, NonmammalianExtracellular MatrixMembrane ProteinsMonomeric GTP-Binding ProteinsNeural CrestXenopus laevisXenopus Proteinscdc42ep1 protein, XenopusCdc42 protein, XenopusCytoskeletal ProteinsMembrane ProteinsMonomeric GTP-Binding ProteinsXenopus Proteins

Identifiers

PMID29040749
PMCPMC6692865
OpenAlexW2763288716

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.