Mutation of mpv17 results in loss of iridophores due to mitochondrial dysfunction in tilapia

Mpv17 (mitochondrial inner membrane protein MPV17) deficiency causes severe mitochondrial DNA depletion syndrome in mammals and loss of pigmentation of iridophores and a significant decrease of melanophores in zebrafish. The reasons for this are still unclear. In this study, we established an mpv17...

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Veröffentlicht in:The Journal of heredity Jg. 116; H. 2; S. 101
Hauptverfasser: Xu, Jia, Li, Peng, Xu, Mengmeng, Wang, Chenxu, Kocher, Thomas D, Wang, Deshou
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States 01.03.2025
Schlagworte:
Animals
Cichlids - genetics
DNA, Mitochondrial - genetics
Fish Proteins - genetics
Melanophores - metabolism
Membrane Proteins - genetics
Mitochondria - genetics
Mitochondrial Proteins - genetics
Mutation
Phenotype
Pigmentation - genetics
melanophore
tilapia
mitochondrial dysfunction
mpv17 mutation
iridophore
ISSN:1465-7333, 1465-7333
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Zusammenfassung:Mpv17 (mitochondrial inner membrane protein MPV17) deficiency causes severe mitochondrial DNA depletion syndrome in mammals and loss of pigmentation of iridophores and a significant decrease of melanophores in zebrafish. The reasons for this are still unclear. In this study, we established an mpv17 homozygous mutant line in Nile tilapia. The developing mutants are transparent due to the loss of iridophores and aggregation of pigment granules in the melanophores and disappearance of the vertical pigment bars on the side of the fish. Transcriptome analysis using the skin of fish at 30 dpf (days post fertilization) revealed that the genes related to purine (especially pnp4a) and melanin synthesis were significantly downregulated. However, administration of guanine diets failed to rescue the phenotype of the mutants. In addition, no obvious apoptosis signals were observed in the iris of the mutants by TUNEL staining. Significant downregulation of genes related to iridophore differentiation was detected by qPCR. Insufficient ATP, as revealed by ATP assay, α-MSH treatment, and adcy5 mutational analysis, might account for the defects of melanophores in mpv17 mutants. Several tissues displayed less mtDNA and decreased ATP levels. Taken together, these results indicated that mutation of mpv17 led to mitochondrial dTMP deficiency, followed by impaired mtDNA content and mitochondrial function, which in turn, led to loss of iridophores and a transparent body color in tilapia.
Bibliographie:ObjectType-Article-1
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content type line 23
ISSN:1465-7333
1465-7333
DOI:10.1093/jhered/esae034