PUBLICATION
A Drosophila model of the neurological symptoms in Mpv17-related diseases
- Authors
- Kodani, A., Yamaguchi, M., Itoh, R., Huynh, M.A., Yoshida, H.
- ID
- ZDB-PUB-230101-8
- Date
- 2022
- Source
- Scientific Reports 12: 2263222632 (Journal)
- Registered Authors
- Keywords
- none
- MeSH Terms
-
- Animals
- DNA, Mitochondrial/genetics
- Drosophila*/genetics
- Drosophila melanogaster*/genetics
- Humans
- Membrane Proteins/genetics
- Mice
- Mitochondrial Proteins/genetics
- Mutation
- Zebrafish/genetics
- PubMed
- 36587049 Full text @ Sci. Rep.
Citation
Kodani, A., Yamaguchi, M., Itoh, R., Huynh, M.A., Yoshida, H. (2022) A Drosophila model of the neurological symptoms in Mpv17-related diseases. Scientific Reports. 12:2263222632.
Abstract
Mutations in the Mpv17 gene are responsible for MPV17-related hepatocerebral mitochondrial DNA depletion syndrome and Charcot-Marie-Tooth (CMT) disease. Although several models including mouse, zebrafish, and cultured human cells, have been developed, the models do not show any neurological defects, which are often observed in patients. Therefore, we knocked down CG11077 (Drosophila Mpv17; dMpv17), an ortholog of human MPV17, in the nervous system in Drosophila melanogaster and investigated the behavioral and cellular phenotypes. The resulting dMpv17 knockdown larvae showed impaired locomotor activity and learning ability consistent with mitochondrial defects suggested by the reductions in mitochondrial DNA and ATP production and the increases in the levels of lactate and reactive oxygen species. Furthermore, an abnormal morphology of the neuromuscular junction, at the presynaptic terminal, was observed in dMpv17 knockdown larvae. These results reproduce well the symptoms of human diseases and partially reproduce the phenotypes of Mpv17-deficient model organisms. Therefore, we suggest that neuron-specific dMpv17 knockdown in Drosophila is a useful model for investigation of MPV17-related hepatocerebral mitochondrial DNA depletion syndrome and CMT caused by Mpv17 dysfunction.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping