Evidence map›Paper›PMID 34057474›Full record

ArticleGenetics2021

Zebrafish spinal cord oligodendrocyte formation requires boc function.

Christina A Kearns, Macie Walker, Andrew M Ravanelli, Kayt Scott, Madeline R Arzbecker, Bruce Appel

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Reciprocal Regulation of Shh Trafficking and HAntioxidants (Basel, Switzerland) · 2022
    Article
  7. Distinct and redundant roles for zebrafishFrontiers in endocrinology · 2022
    Article
  8. Article
  9. Review
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 1 institution in 1 country.

Christina A KearnsDepartment of Pediatrics, Section of Developmental Biology, University of Colorado Anschutz Medical Campus and Children's Hospital Colorado, Aurora, CO 80045, USA.
Macie WalkerDepartment of Pediatrics, Section of Developmental Biology, University of Colorado Anschutz Medical Campus and Children's Hospital Colorado, Aurora, CO 80045, USA.
Andrew M RavanelliDepartment of Pediatrics, Section of Developmental Biology, University of Colorado Anschutz Medical Campus and Children's Hospital Colorado, Aurora, CO 80045, USA.ORCID 0000-0001-8138-3880
Kayt ScottDepartment of Pediatrics, Section of Developmental Biology, University of Colorado Anschutz Medical Campus and Children's Hospital Colorado, Aurora, CO 80045, USA.ORCID 0000-0003-4552-2032
Madeline R ArzbeckerDepartment of Pediatrics, Section of Developmental Biology, University of Colorado Anschutz Medical Campus and Children's Hospital Colorado, Aurora, CO 80045, USA.
Bruce AppelDepartment of Pediatrics, Section of Developmental Biology, University of Colorado Anschutz Medical Campus and Children's Hospital Colorado, Aurora, CO 80045, USA.ORCID 0000-0003-4500-0672
Children's Hospital Colorado · 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
Prdm8 inhibits oligodendrocyte differentiation through gene repressionF31NS116922 · NINDS · UNIVERSITY OF COLORADO DENVER · PI SCOTT, KATHRYN F · 2020 to 2020
$27k
NIH HHS F31 NS116922NIH HHS P30 NS048154NIH HHS T32 CA08208613NINDS NIH HHS F31 NS116922NINDS NIH HHS P30 NS048154
6 · The paper itself

Abstract

The axis of the vertebrate neural tube is patterned, in part, by a ventral to dorsal gradient of Shh signaling. In the ventral spinal cord, Shh induces concentration-dependent expression of transcription factors, subdividing neural progenitors into distinct domains that subsequently produce distinct neuronal and glial subtypes. In particular, progenitors of the pMN domain express the bHLH transcription factor Olig2 and produce motor neurons followed by oligodendrocytes, the myelinating glial cell type of the central nervous system. In addition to its role in patterning ventral progenitors, Shh signaling must be maintained through development to specify pMN progenitors for oligodendrocyte fate. Using a forward genetic screen in zebrafish for mutations that disrupt the development of oligodendrocytes, we identified a new mutant allele of boc, which encodes a type I transmembrane protein that functions as a coreceptor for Shh. Embryos homozygous for the bocco25 allele, which creates a missense mutation in a Fibronectin type III domain that binds Shh, have normally patterned spinal cords but fail to maintain pMN progenitors, resulting in a deficit of oligodendrocytes. Using a sensitive fluorescent detection method for in situ RNA hybridization, we found that spinal cord cells express boc in a graded fashion that is inverse to the gradient of Shh signaling activity and that boc function is necessary to maintain pMN progenitors by shaping the Shh signaling gradient.

Indexed as

NeurogenesisAnimalsNeural Cell Adhesion MoleculesNeural Stem CellsOligodendrogliaSpinal CordZebrafishZebrafish ProteinsBOC protein, zebrafishNeural Cell Adhesion MoleculesZebrafish Proteinsgliamyelinneural progenitorsoligodendrocyte precursor cellssonic hedgehog

Identifiers

PMID34057474
PMCPMC8864740
OpenAlexW3164339852

What Socratic 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 Socratic graph.