Evidence map›Paper›PMID 35820658›Full record

ArticleDevelopmental biology2022

Peripheral nerve development in zebrafish requires muscle patterning by tcf15/paraxis.

Lauren E Limbach, Rocky L Penick, Rudy S Casseday, Maddelyn A Hyland, Erika A Pontillo, Afomia N Ayele, Kristen M Pitts, Sarah D Ackerman, Breanne L Harty, Amy L Herbert and 2 more

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

12 authors at 2 institutions in 1 country.

Lauren E LimbachDepartment of Neuroscience, Kenyon College, Gambier, OH, USA.
Rocky L PenickDepartment of Neuroscience, Kenyon College, Gambier, OH, USA.
Rudy S CassedayDepartment of Neuroscience, Kenyon College, Gambier, OH, USA.
Maddelyn A HylandDepartment of Neuroscience, Kenyon College, Gambier, OH, USA.
Erika A PontilloDepartment of Biology, Kenyon College, Gambier, OH, USA.
Afomia N AyeleDepartment of Neuroscience, Kenyon College, Gambier, OH, USA.
Kristen M PittsDepartment of Biology, Kenyon College, Gambier, OH, USA.
Sarah D AckermanDepartment of Developmental Biology, Washington University in St. Louis, MO, USA.
Breanne L HartyDepartment of Developmental Biology, Washington University in St. Louis, MO, USA.
Amy L HerbertDepartment of Developmental Biology, Washington University in St. Louis, MO, USA.
Kelly R MonkDepartment of Developmental Biology, Washington University in St. Louis, MO, USA.
Sarah C PetersenDepartment of Neuroscience, Kenyon College, Gambier, OH, USA; Department of Biology, Kenyon College, Gambier, OH, USA; Department of Developmental Biology, Washington University in St. Louis, MO, USA. Electronic address: petersens@kenyon.edu.
Kenyon College · USWashington University in St. Louis · US

Funding

Chemical and genetic screens for modulators of nervous system development and myelinationR01HD080601 · NICHD · WASHINGTON UNIVERSITY · PI MONK, KELLY R · 2014 to 2018
$1.6M
DISSECTING MOLECULAR AND GENETIC MECHANISMS THAT PROMOTE MYELINATIONF32NS087786 · NINDS · WASHINGTON UNIVERSITY · PI PETERSEN, SARAH · 2014 to 2016
$131k
NICHD NIH HHS R01 HD080601NINDS NIH HHS F32 NS087786
6 · The paper itself

Abstract

The vertebrate peripheral nervous system (PNS) is an intricate network that conveys sensory and motor information throughout the body. During development, extracellular cues direct the migration of axons and glia through peripheral tissues. Currently, the suite of molecules that govern PNS axon-glial patterning is incompletely understood. To elucidate factors that are critical for peripheral nerve development, we characterized the novel zebrafish mutant, stl159, that exhibits abnormalities in PNS patterning. In these mutants, motor and sensory nerves that develop adjacent to axial muscle fail to extend normally, and neuromasts in the posterior lateral line system, as well as neural crest-derived melanocytes, are incorrectly positioned. The stl159 genetic lesion lies in the basic helix-loop-helix (bHLH) transcription factor tcf15, which has been previously implicated in proper development of axial muscles. We find that targeted loss of tcf15 via CRISPR-Cas9 genome editing results in the PNS patterning abnormalities observed in stl159 mutants. Because tcf15 is expressed in developing muscle prior to nerve extension, rather than in neurons or glia, we predict that tcf15 non-cell-autonomously promotes peripheral nerve patterning in zebrafish through regulation of extracellular patterning cues. Our work underscores the importance of muscle-derived factors in PNS development.

Indexed as

Peripheral NervesZebrafishAnimalsAxonsBasic Helix-Loop-Helix ProteinsMusclesPeripheral Nervous SystemBasic Helix-Loop-Helix ProteinsLateral line nerveMyelinParaxial mesodermSchwann cellsZebrafish

Identifiers

PMID35820658
PMCPMC10935611
OpenAlexW4284993240

What OpenQuestion holds

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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.