Evidence map›Paper›PMID 19301392›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2009

Transcriptional control of Rohon-Beard sensory neuron development at the neural plate border.

Christy Cortez Rossi, Takao Kaji, Kristin Bruk Artinger

Open access · bronzeAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Single-Cell Analysis of Rohon-Beard Neurons Implicates Fgf Signaling in Axon Maintenance and Cell Survival.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. piezo2b regulates vertebrate light touch response.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

3 authors at 1 institution in 1 country.

Christy Cortez RossiDepartment of Craniofacial Biology, University of Colorado, Denver, Colorado 80010, USA.
Takao Kaji
Kristin Bruk Artinger
University of Colorado Denver · US

Funding

ZEBRAFISH TRANSGENIC CORE - ROCKY MOUNTAIN NEUROLOGICAL DISORDERS CORE CENTERP30NS048154 · NINDS · UNIVERSITY OF COLORADO DENVER · PI RIBERA, ANGELES BADELL · 2004 to 2020
$10.1M
NEUROSCIENCE TRAINING GRANTT32HD041697 · NICHD · UNIVERSITY OF COLORADO DENVER · PI RESTREPO, DIEGO · 2001 to 2015
$2.4M
The role of prdm1 in neural cell fate specificationR01HD050698 · NICHD · UNIVERSITY OF COLORADO DENVER · PI ARTINGER, KRISTIN · 2006 to 2010
$1.2M
NICHD NIH HHS HD41697-03NICHD NIH HHS R01 HD050698NICHD NIH HHS R01 HD0506986NICHD NIH HHS R01 HD50698NINDS NIH HHS P30 NS048154
6 · The paper itself

Abstract

Rohon-Beard (RB) mechanosensory neurons are among the first sensory neurons to develop, and the process by which they adopt their fate is not completely understood. RBs form at the neural plate border (NPB), the junction between neural and epidermal ectoderm, and require the transcription factor prdm1a. Here, we show that prior to RB differentiation, prdm1a overlaps extensively with the epidermal marker dlx3b but shows little overlap with the neuroectodermal markers sox3 and sox19a. Birthdating analysis reveals that the majority of RBs are born during gastrulation in zebrafish, suggesting that it is during this period that RBs become specified. Expression analysis in prdm1a and neurogenin1 mutant and dlx3b/dlx4b morpholino-injected embryos suggests that prdm1a is upstream of dlx3b, dlx4b, and neurogenin1 at the NPB. mRNA for neurogenin1 or dlx3b/dlx4b can rescue the lack of RBs in prdm1a mutants. Based on these data, we suggest a preliminary gene regulatory network for RB development.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsDNA-Binding ProteinsGastrulationGene Expression Regulation, DevelopmentalHomeodomain ProteinsNerve Tissue ProteinsNeural PlateNeurogenesisNuclear ProteinsPositive Regulatory Domain I-Binding Factor 1Sensory Receptor CellsSOXB1 Transcription FactorsTranscription, GeneticZebrafishZebrafish ProteinsBasic Helix-Loop-Helix Proteinsdlx3b protein, zebrafishDNA-Binding ProteinsHomeodomain ProteinsNerve Tissue Proteinsneurog1 protein, zebrafishNuclear ProteinsPositive Regulatory Domain I-Binding Factor 1prdm1a protein, zebrafishSOXB1 Transcription FactorsZebrafish Proteins

Identifiers

PMID19301392
PMCPMC2755227
OpenAlexW2058825331

What OpenQuestion holds

Textmetadata
LicenceTDM
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.