PUBLICATION

Deficiency of psmb6 suppresses proteasome activity and promotes apoptosis in larval zebrafish brain

Authors
Xiao, W., Cheng, J., Zhang, L., Li, X., Zhang, J., Ning, G.
ID
ZDB-PUB-250307-22
Date
2025
Source
Biochemical and Biophysical Research Communications   755: 151574151574 (Journal)
Registered Authors
Zhang, Jingjing
Keywords
Apoptosis, Proteasome, Zebrafish, psmb6
MeSH Terms
  • Apoptosis*/genetics
  • Proteasome Endopeptidase Complex*/genetics
  • Proteasome Endopeptidase Complex*/metabolism
  • Zebrafish*/embryology
  • Zebrafish*/genetics
  • Zebrafish*/metabolism
  • Neurons/metabolism
  • Neurons/pathology
  • Tumor Suppressor Protein p53/deficiency
  • Tumor Suppressor Protein p53/genetics
  • Tumor Suppressor Protein p53/metabolism
  • Brain*/metabolism
  • Zebrafish Proteins*/deficiency
  • Zebrafish Proteins*/genetics
  • Zebrafish Proteins*/metabolism
  • Animals
  • Larva*/genetics
  • Larva*/growth & development
  • Larva*/metabolism
PubMed
40048760 Full text @ Biochem. Biophys. Res. Commun.
Abstract
In humans, the abnormal accumulation of proteins is strongly correlated with neurodegenerative diseases. PSMB6 is a member of the proteasome family and encodes the 20S subunit beta 6 which performs caspase-like proteasome activity. However, the biological roles of PSMB6 in neurodevelopment are poorly defined. In this study, we utilized zebrafish to construct a psmb6 knockout model. We show that the deficiency of psmb6 leads to early embryonic death, with proteasome inactivity identified as the cause of neuronal apoptosis. Although the inactivation of p53 cannot rescue the defects observed in psmb6 mutants, it delays the onset of the defective phenotypes. Thus, psmb6 plays a crucial role in early embryonic development.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping