Evidence map›Paper›PMID 23122226›Full record

ArticleNeural development2012

Zebrafish Mnx proteins specify one motoneuron subtype and suppress acquisition of interneuron characteristics.

Steve D Seredick, Liesl Van Ryswyk, Sarah A Hutchinson, Judith S Eisen

Open access · goldAbstract read
In one paragraph

Article in Neural development, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

34 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Electrical Synapses Mediate Embryonic Hyperactivity in a Zebrafish Model of Fragile X Syndrome.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  5. Article
  6. In Vivo Optogenetic Phase Transition of an Intrinsically Disordered Protein.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
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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

4 authors at 2 institutions in 2 countries.

Steve D SeredickInstitute of Neuroscience, University of Oregon, Eugene, OR, USA.
Liesl Van Ryswyk
Sarah A Hutchinson
Judith S Eisen
University of Oregon · USHospital for Sick Children · CA

Funding

Zebrafish FacilityP01HD022486 · NICHD · UNIVERSITY OF OREGON · PI EISEN, JUDITH S · 1987 to 2017
$28.8M
DEVELOPMENTAL BIOLOGY TRAINING PROGRAMT32HD007348 · NICHD · UNIVERSITY OF OREGON · PI Chris Q Doe, KRYN STANKUNAS · 1989 to 2026
$6.8M
NEURONAL PATHFINDING BY IDENTIFIED MOTONEURONSR01NS023915 · NINDS · UNIVERSITY OF OREGON · PI EISEN, JUDITH S · 1986 to 2012
$5.0M
Development of Identified MotoneuronsR56NS023915 · NINDS · UNIVERSITY OF OREGON · PI EISEN, JUDITH S · 2007 to 2007
$467k
NICHD NIH HHS HD007348NICHD NIH HHS HD22486NICHD NIH HHS T32 HD007348NINDS NIH HHS NS23915
6 · The paper itself

Abstract

backgroundPrecise matching between motoneuron subtypes and the muscles they innervate is a prerequisite for normal behavior. Motoneuron subtype identity is specified by the combination of transcription factors expressed by the cell during its differentiation. Here we investigate the roles of Mnx family transcription factors in specifying the subtypes of individually identified zebrafish primary motoneurons.

resultsZebrafish has three Mnx family members. We show that each of them has a distinct and temporally dynamic expression pattern in each primary motoneuron subtype. We also show that two Mnx family members are expressed in identified VeLD interneurons derived from the same progenitor domain that generates primary motoneurons. Surprisingly, we found that Mnx proteins appear unnecessary for differentiation of VeLD interneurons or the CaP motoneuron subtype. Mnx proteins are, however, required for differentiation of the MiP motoneuron subtype. We previously showed that MiPs require two temporally-distinct phases of Islet1 expression for normal development. Here we show that in the absence of Mnx proteins, the later phase of Islet1 expression is initiated but not sustained, and MiPs become hybrids that co-express morphological and molecular features of motoneurons and V2a interneurons. Unexpectedly, these hybrid MiPs often extend CaP-like axons, and some MiPs appear to be entirely transformed to a CaP morphology.

conclusionsOur results suggest that Mnx proteins promote MiP subtype identity by suppressing both interneuron development and CaP axon pathfinding. This is, to our knowledge, the first report of transcription factors that act to distinguish CaP and MiP subtype identities. Our results also suggest that MiP motoneurons are more similar to V2 interneurons than are CaP motoneurons.

Indexed as

AnimalsAnimals, Genetically ModifiedCell DifferentiationEmbryo, NonmammalianGene Expression Regulation, DevelopmentalGreen Fluorescent ProteinsInterneuronsLIM-Homeodomain ProteinsMorpholinosMotor NeuronsSpinal CordTranscription FactorsZebrafishZebrafish ProteinsGreen Fluorescent Proteinsinsulin gene enhancer binding protein Isl-1LIM-Homeodomain ProteinsMnx1 protein, zebrafishMorpholinosTranscription FactorsZebrafish Proteins

Identifiers

PMID23122226
PMCPMC3570319
OpenAlexW2123509007

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.