Evidence map›Paper›PMID 30242148›Full record

ArticleNature communications2018

Gap junction protein Connexin-43 is a direct transcriptional regulator of N-cadherin in vivo.

Maria Kotini, Elias H Barriga, Jonathan Leslie, Marc Gentzel, Verena Rauschenberger, Alexandra Schambony, Roberto Mayor

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 120 papers.

0numbers the graph read from it
0cells of the map it votes in
120citing papers in PubMed
6.6field-weighted citation impact, top 2% 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

120 citing papers in PubMed, 172 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Beyond the gap: moonlighting functions of connexins in cancer.Cell communication and signaling : CCS · 2026
    Review
  5. Article
  6. Macrophages sense and follow physiologically relevant KCell communication and signaling : CCS · 2026
    Article
  7. Review
  8. Article
  9. Connexin 26 Functions as a Direct Transcriptional Regulator During the Cochlea Development.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  10. Article
  11. Deceiving the gatekeepers: virus modulation of gap junctions.Microbiology and molecular biology reviews : MMBR · 2025
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article

60 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 2 countries.

Maria KotiniDepartment of Cell and Developmental Biology, University College London, Gower Street, London, WC1E 6BT, UK.
Elias H BarrigaDepartment of Cell and Developmental Biology, University College London, Gower Street, London, WC1E 6BT, UK.
Jonathan LeslieDepartment of Cell and Developmental Biology, University College London, Gower Street, London, WC1E 6BT, UK.
Marc GentzelMax Planck Institut for Molecular Cell Biology and Genetics, Pfotenhauerstr. 108, 01307, Dresden, Germany.
Verena RauschenbergerBiology Department, Developmental Biology, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, 91058, Germany.
Alexandra SchambonyBiology Department, Developmental Biology, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, 91058, Germany.ORCID http://orcid.org/0000-0001-8771-5487
Roberto MayorDepartment of Cell and Developmental Biology, University College London, Gower Street, London, WC1E 6BT, UK. r.mayor@ucl.ac.uk.
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEUniversity College London · GBCenter for Systems Biology Dresden · DELondon Centre for Nanotechnology · GBMRC Laboratory for Molecular Cell Biology · GB

Funding

Biotechnology and Biological Sciences Research Council (BBSRC) M008517Medical Research Council (MRC) M010465Wellcome Trust
6 · The paper itself

Abstract

Connexins are the primary components of gap junctions, providing direct links between cells under many physiological processes. Here, we demonstrate that in addition to this canonical role, Connexins act as transcriptional regulators. We show that Connexin 43 (Cx43) controls neural crest cell migration in vivo by directly regulating N-cadherin transcription. This activity requires interaction between Cx43 carboxy tail and the basic transcription factor-3, which drives the translocation of Cx43 tail to the nucleus. Once in the nucleus they form a complex with PolII which directly binds to the N-cadherin promoter. We found that this mechanism is conserved between amphibian and mammalian cells. Given the strong evolutionary conservation of connexins across vertebrates, this may reflect a common mechanism of gene regulation by a protein whose function was previously ascribed only to gap junctional communication.

Indexed as

Gene Expression RegulationAnimalsCadherinsCell MovementConnexin 43DNA Polymerase IIHeLa CellsHumansNeural CrestNuclear ProteinsTranscription FactorsXenopus laevisCadherinsConnexin 43DNA Polymerase IINuclear Proteinstranscription factor BTF3Transcription Factors

Identifiers

PMID30242148
PMCPMC6155008
OpenAlexW2891288279

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.