Evidence map›Paper›PMID 18406403›Full record

ArticleDevelopmental biology2008

Connexin43 (GJA1) is required in the population of dividing cells during fin regeneration.

Angela D Hoptak-Solga, Sarah Nielsen, Isha Jain, Ryan Thummel, David R Hyde, M Kathryn Iovine

Open access · greenAbstract readComparative Study
In one paragraph

Article in Developmental biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

48 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Retinoic Acid InfluencesBioelectricity · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Calcineurin controls proximodistal blastema polarity in zebrafish fin regeneration.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Connexin Communication Compartments and Wound Repair in Epithelial Tissue.International journal of molecular sciences · 2018
    Review
  20. 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.

Angela D Hoptak-SolgaLehigh University, Department of Biological Sciences, 111 Research Drive, Iacocca B-217, Bethlehem, PA 18015, USA.
Sarah Nielsen
Isha Jain
Ryan Thummel
David R Hyde
M Kathryn Iovine
Lehigh University · USUniversity of Notre Dame · US

Funding

Gap junctional communication during zebrafish fin growthR01HD047737 · NICHD · LEHIGH UNIVERSITY · PI IOVINE, MARY KATHRYN · 2005 to 2009
$1.1M
Development of Genetic Tools to Study Retinal Regeneration R21EY017134 · NEI · UNIVERSITY OF NOTRE DAME · PI HYDE, DAVID R · 2006 to 2007
$370k
NEI NIH HHS R21 EY017134NEI NIH HHS R21-EY017134NICHD NIH HHS HD047737NICHD NIH HHS R01 HD047737
6 · The paper itself

Abstract

In zebrafish, mutations in the gap junction gene connexin43 lead to short bony fin ray segments that give rise to the short fin phenotype. The sof(b123) mutant exhibits fins that are half the length of wild-type fins and have reduced levels of cx43 mRNA. We find that sof(b123) regenerating fins exhibit reduced levels of cell proliferation. Interestingly, the number of dividing cells per unit length of fin growth is similar between wild-type and mutant fins, suggesting that the number of cells that enter the cell cycle is specifically affected in sof(b123). Expression of cx43 is identified in mitotic cells, which further suggests that Cx43 may contribute to establishing or maintaining the population of dividing cells. Indeed, missense alleles exhibiting high or low levels of gap junctional communication reveal a correlation between defects in direct cell-cell communication, cell proliferation, and segment length. Finally, targeted gene knockdown of cx43 in adult regenerating fins recapitulates the sof(b123) phenotype, revealing that the loss of Cx43 is sufficient to reduce both cell proliferation and segment length. We hypothesize that the level of gap junctional intercellular communication among dividing cells regulates the level of cell proliferation and ultimately regulates bone growth.

Indexed as

AnimalsAnimal StructuresCell CommunicationCell ProliferationConnexin 43CryoultramicrotomyElectroporationGap JunctionsImmunoblottingIn Situ HybridizationMutationRegenerationZebrafishConnexin 43

Identifiers

PMID18406403
PMCPMC2429987
OpenAlexW2136590846

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.