PUBLICATION

Role and Impact of the brsk2 Gene in Zebrafish Retinal Development and Visual Function Characterized by Behavioral, Histological, and Transcriptomic Analyses

Authors
Deng, J., Li, Y., Hu, M., Hu, C., Lin, J., Li, Q., Xu, X., Liu, C.
ID
ZDB-PUB-260129-33
Date
2026
Source
International Journal of Molecular Sciences   27: (Journal)
Registered Authors
Li, Qiang, Liu, Chunxue, Xu, Xiu
Keywords
BRSK2, autism spectrum disorder, vision function, zebrafish
MeSH Terms
  • Animals
  • Behavior, Animal
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental
  • Protein Serine-Threonine Kinases*/genetics
  • Protein Serine-Threonine Kinases*/metabolism
  • Retina*/growth & development
  • Retina*/metabolism
  • Transcriptome*
  • Vision, Ocular*/genetics
  • Zebrafish*/genetics
  • Zebrafish*/growth & development
  • Zebrafish Proteins*/genetics
  • Zebrafish Proteins*/metabolism
PubMed
41596506 Full text @ Int. J. Mol. Sci.
Abstract
Vision is fundamental to the acquisition of motor, cognitive, and social skills, playing a crucial role in typical development. Early visual impairments are associated with various neurodevelopmental conditions, including Autism Spectrum Disorder (ASD). The (Brain-specific serine/threonine-protein kinase 2, BRSK2) gene has been identified as a high-risk gene for ASD. This study aims to investigate the role of brsk2 in retinal photoreceptor development and visual function in zebrafish. Using behavioral assays, histological analysis, and transcriptomic profiling, we assessed the impact of brsk2 deletion on retinal structure and function. The results showed that brsk2ab-/- zebrafish larvae exhibited significantly enhanced light perception compared to wild-type (WT) controls. Structural analysis of the retina revealed disruptions in the layered organization, along with up-regulated rhodopsin expression in retinal cells. Additionally, transcriptomic analysis indicated that key opsins and genes involved in visual development and phototransduction pathways were markedly up-regulated following brsk2 deletion. This research highlights the importance of brsk2 in early retinal circuit development and its potential implications for understanding sensory processing deficits in neurodevelopmental disorders. By linking BRSK2 to specific sensory phenotypes, this study addresses a critical gap in knowledge regarding the mechanisms underlying sensory abnormalities in ASD and related conditions.
Genes / Markers
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping