Evidence map›Paper›PMID 25231761›Full record

ArticleDevelopment (Cambridge, England)2014

Lhx3 and Lhx4 suppress Kolmer-Agduhr interneuron characteristics within zebrafish axial motoneurons.

Steve Seredick, Sarah A Hutchinson, Liesl Van Ryswyk, Jared C Talbot, Judith S Eisen

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.1field-weighted citation impact, top 45% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Regulation of motor neuron differentiation in thebioRxiv : the preprint server for biology · 2025
    Article
  4. LHX3 promotes EMT in hepatoma cell through β-catenin/TCF4 pathway.Medical oncology (Northwood, London, England) · 2024
    Article
  5. Article
  6. Combined Pituitary Hormone Deficiency inInternational journal of molecular sciences · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. 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

5 authors at 1 institution in 1 country.

Steve SeredickInstitute of Neuroscience, 1254 University of Oregon, Eugene, OR 97403, USA.
Sarah A HutchinsonInstitute of Neuroscience, 1254 University of Oregon, Eugene, OR 97403, USA.
Liesl Van RyswykInstitute of Neuroscience, 1254 University of Oregon, Eugene, OR 97403, USA.
Jared C TalbotInstitute of Neuroscience, 1254 University of Oregon, Eugene, OR 97403, USA.
Judith S EisenInstitute of Neuroscience, 1254 University of Oregon, Eugene, OR 97403, USA eisen@uoneuro.uoregon.edu.
University of Oregon · US

Funding

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 T32 HD007348NINDS NIH HHS NS23915NINDS NIH HHS R01 NS023915NINDS NIH HHS R56 NS023915
6 · The paper itself

Abstract

A central problem in development is how fates of closely related cells are segregated. Lineally related motoneurons (MNs) and interneurons (INs) express many genes in common yet acquire distinct fates. For example, in mouse and chick Lhx3 plays a pivotal role in the development of both cell classes. Here, we utilize the ability to recognize individual zebrafish neurons to examine the roles of Lhx3 and its paralog Lhx4 in the development of MNs and ventral INs. We show that Lhx3 and Lhx4 are expressed by post-mitotic axial MNs derived from the MN progenitor (pMN) domain, p2 domain progenitors and by several types of INs derived from pMN and p2 domains. In the absence of Lhx3 and Lhx4, early-developing primary MNs (PMNs) adopt a hybrid fate, with morphological and molecular features of both PMNs and pMN-derived Kolmer-Agduhr' (KA') INs. In addition, we show that Lhx3 and Lhx4 distinguish the fates of two pMN-derived INs. Finally, we demonstrate that Lhx3 and Lhx4 are necessary for the formation of late-developing V2a and V2b INs. In conjunction with our previous work, these data reveal that distinct transcription factor families are deployed in post-mitotic MNs to unequivocally assign MN fate and suppress the development of alternative pMN-derived IN fates.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsAxonsCell LineageGene Expression ProfilingGreen Fluorescent ProteinsInterneuronsLIM-Homeodomain ProteinsMotor NeuronsNeuronsOligonucleotidesPhenotypeProtein Structure, TertiarySignal TransductionSpinal CordTranscription FactorsGreen Fluorescent ProteinsLhx3 proteinLhx4 protein, zebrafishLIM-Homeodomain ProteinsOligonucleotidesTranscription FactorsZebrafish ProteinsInterneuronKolmer–AgduhrLhx3Lhx4MotoneuronV2aV2bZebrafish

Identifiers

PMID25231761
PMCPMC4197711
OpenAlexW2140225526

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.