Evidence map›Paper›PMID 41890051›Full record

ArticlebioRxiv : the preprint server for biology2026

TALE and Hox Transcription Factors Control Adult Behaviors in Zebrafish.

Austin Adkins, Katelyn Glowinski, Yong-Il Kim, Ethan Wright, Cameron E Bennett, Jessica C Nelson, Charles G Sagerström

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Austin AdkinsSection of Developmental Biology, Department of Pediatrics, University of Colorado Anschutz, Aurora, CO, USA.
Katelyn GlowinskiSection of Developmental Biology, Department of Pediatrics, University of Colorado Anschutz, Aurora, CO, USA.
Yong-Il KimSection of Developmental Biology, Department of Pediatrics, University of Colorado Anschutz, Aurora, CO, USA.
Ethan WrightSection of Developmental Biology, Department of Pediatrics, University of Colorado Anschutz, Aurora, CO, USA.
Cameron E BennettSection of Developmental Biology, Department of Pediatrics, University of Colorado Anschutz, Aurora, CO, USA.
Jessica C NelsonDepartment of Cell and Developmental Biology, University of Colorado Anschutz, Aurora, CO, USA.
Charles G SagerströmSection of Developmental Biology, Department of Pediatrics, University of Colorado Anschutz, Aurora, CO, USA.ORCID 0000-0002-1509-5810

Funding

In vivo motif selectivity and functionality of TALE family TFsR01GM142158 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI SAGERSTROM, CHARLES G · 2021 to 2024
$1.6M
Understanding the molecular function and substrate specificity of palmitoyltransferases in regulating behaviorR35GM159847 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI Jessica C Nelson · 2025 to 2026
$780k
NIGMS NIH HHS R01 GM142158NIGMS NIH HHS R35 GM159847
6 · The paper itself

Abstract

Behavioral dysfunction is a common characteristic of many mental health disorders. While the causes of these disorders vary, aberrant behaviors may arise from alterations in transcriptional regulation already during early neural development. Because transcription factors (TFs) often belong to families of closely related members, disruption of a single TF may indirectly influence the functionality of other family members. Consequently, mutations in TFs within the same family may lead to overlapping, yet distinct, phenotypes. This feature of TF function has important implications for understanding behavioral phenotypes, but detailed analyses across a single TF family are still lacking. In this study, we present a comprehensive behavioral analysis of adult zebrafish harboring mutations in individual members of the TALE and Hox TF families, that are essential for nervous system development. Using a battery of validated behavioral assays, we uncover elevated stress responses among all TF mutant lines, as well as TF-specific dysregulation in coping strategies, social interaction, learning/memory, and endurance and locomotion. The shared behavioral abnormalities across mutants suggests TF family members converge on core developmental pathways for stress-related behavioral regulation, while mutation-specific phenotypes indicate unique roles for individual TFs in fine-tuning neural function. Our findings provide a systematic behavioral characterization of TALE and Hox mutants in a vertebrate model and provide a framework for understanding how genetic variation within TF families may differentially contribute to vulnerability for mental health disorders.

Indexed as

Gene Function in BehaviorMental HealthTALE and Hox genesTranscriptional Regulation

Identifiers

PMID41890051
PMCPMC13015412

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Registered trials

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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.