PUBLICATION

Novel Degenerative and Developmental Defects in a Zebrafish Model of Mucolipidosis Type IV

Authors
Li, H., Pei, W., Vergarajauregui, S., Zerfas, P.M., Raben, N., Burgess, S.M., Puertollano, R.
ID
ZDB-PUB-170428-2
Date
2017
Source
Human molecular genetics   26(14): 2701-2718 (Journal)
Registered Authors
Burgess, Shawn, Pei, Wuhong, Puertollano, Rosa, Raben, Nina
Keywords
immunohistochemistry, embryo, genes, auditory hair cell, zebrafish, pathology, mucolipidosis iv, autophagosomes
MeSH Terms
  • Amino Acid Sequence
  • Animals
  • Autophagosomes/metabolism
  • Disease Models, Animal
  • Gene Knockout Techniques
  • Mucolipidoses/genetics*
  • Mucolipidoses/metabolism
  • Mucolipidoses/pathology
  • Mutation
  • Transient Receptor Potential Channels/genetics*
  • Transient Receptor Potential Channels/metabolism
  • Zebrafish
  • Zebrafish Proteins/genetics*
  • Zebrafish Proteins/metabolism
PubMed
28449103 Full text @ Hum. Mol. Genet.
Abstract
Mucolipidosis type IV (MLIV) is a lysosomal storage disease characterized by neurologic and ophthalmologic abnormalities. There is currently no effective treatment. MLIV is caused by mutations in MCOLN1, a lysosomal cation channel from the transient receptor potential (TRP) family. In this study we used genome editing to knockout the two mcoln1 genes present in Danio rerio (zebrafish). Our model successfully reproduced the retinal and neuromuscular defects observed in MLIV patients, indicating that this model is suitable for studying the disease pathogenesis. Importantly, our model revealed novel insights into the origins and progression of the MLIV pathology, including the contribution of autophagosome accumulation to muscle dystrophy and the role of mcoln1 in embryonic development, hair cell viability and cellular maintenance. The generation of a MLIV model in zebrafish is particularly relevant given the suitability of this organism for large-scale in vivo drug screening, thus providing unprecedented opportunities for therapeutic discovery.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping