PUBLICATION

Bi-Allelic Mutations in Zebrafish pank2 Gene Lead to Testicular Atrophy and Perturbed Behavior without Signs of Neurodegeneration

Authors
Mignani, L., Zizioli, D., Khatri, D., Facchinello, N., Schiavone, M., De Palma, G., Finazzi, D.
ID
ZDB-PUB-221115-30
Date
2022
Source
International Journal of Molecular Sciences   23(21): (Journal)
Registered Authors
Facchinello, Nicola, Finazzi, Dario, Schiavone, Marco
Keywords
Coenzyme A, PANK2, iron, neurodegeneration, zebrafish
MeSH Terms
  • Animals
  • Atrophy
  • Coenzyme A/genetics
  • Mutation
  • Pantothenate Kinase-Associated Neurodegeneration*/genetics
  • Pantothenate Kinase-Associated Neurodegeneration*/pathology
  • Phosphotransferases (Alcohol Group Acceptor)/metabolism
  • Zebrafish*/genetics
  • Zebrafish*/metabolism
PubMed
36361705 Full text @ Int. J. Mol. Sci.
Abstract
Coenzyme A (CoA) is an essential cofactor in all living organisms, being involved in a large number of chemical reactions. Sequence variations in pantothenate kinase 2 (PANK2), the first enzyme of CoA biosynthesis, are found in patients affected by Pantothenate Kinase Associated Neurodegeneration (PKAN), one of the most common forms of neurodegeneration, with brain iron accumulation. Knowledge about the biochemical and molecular features of this disorder has increased a lot in recent years. Nonetheless, the main culprit of the pathology is not well defined, and no treatment option is available yet. In order to contribute to the understanding of this disease and facilitate the search for therapies, we explored the potential of the zebrafish animal model and generated lines carrying biallelic mutations in the pank2 gene. The phenotypic characterization of pank2-mutant embryos revealed anomalies in the development of venous vascular structures and germ cells. Adult fish showed testicular atrophy and altered behavioral response in an anxiety test but no evident signs of neurodegeneration. The study suggests that selected cell and tissue types show a higher vulnerability to pank2 deficiency in zebrafish. Deciphering the biological basis of this phenomenon could provide relevant clues for better understanding and treating PKAN.
Genes / Markers
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping