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September 12, 2025Brain Research BulletinOpen Access

Mutation of ube3a causes developmental abnormalities and autism-like molecular and behavioral alterations in zebrafish

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Authors

GDGodfried DougnonLRLana RummelHMHideaki Matsui

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Overview

This study demonstrates developmental abnormalities and behavioral changes in zebrafish with UBE3A mutation, suggesting links to neurodevelopmental disorders.

Key Points

  • Developmental abnormalities were noted in zebrafish models with a mutation in the ube3a gene, causing significant implications for neurodevelopment.
  • Behavioral analyses indicated locomotor deficits and reduced social interactions in mutant zebrafish, aligning with profiles seen in neurodevelopmental disorders.
  • RNA sequencing revealed dysregulation of critical genes associated with chromatin and protein-DNA interactions, highlighting the mutation's molecular impact.
  • The findings establish zebrafish as a viable model for studying UBE3A-related neurodevelopment and behavior alterations, aiming to elucidate its role in disorders.

Cite This Study

Dougnon et al. (2025) studied this question.

synapsesocial.com/papers/68d41dae713b0b5dfea67446https://doi.org/10.1016/j.brainresbull.2025.111542
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Mutation of Brain Aromatase Impairs Behavior and Neuroplasticity in Adult Zebrafish2025
  2. 2UBE3A reinstatement restores behaviorand proteome in an Angelman syndrome mouse model of imprinting defects2025 · 5 citations
  3. 3Cell type-specific contributions of UBE3A to Angelman syndrome behavioral phenotypes2025 · 2 citations
  4. 4Multi-targeting zinc finger nuclease vector unsilences paternal UBE3A in a mouse model of Angelman syndrome2025
  5. 5A de novo mutation in RAB11A is associated with neurodevelopmental disorder accompanied by variable multisystem abnormalities2025