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Tilapia as an economically important fish is also an excellent model for studying pigment cell biology and body color formation. In the present study, we engineered a red tilapia by mutation of hps5 using CRISPR/Cas9 gene editing of a target site in exon 2. Disruption of HPS5 led to a significant decrease in the numbers of melanophores and iridophores, and a significant increase in xanthophores, which led to a yellowish-transparent body color in early stages (5–30 dpf, days post fertilization). Slow recovery of iridophore numbers, and increased numbers of xanthophores with shorter nearest-neighbor distances than in wild-type fish was observed at 150 dpf, which finally led to a red tilapia with reddish pigmentation in fins. The hps5−/− mutants also showed several transparent cracks (absence of melanin, iridophores and xanthophores) in iris development. Besides, hps5 was also found to be fundamental for xanthophore development, and even the distance between each of them. Our hps5 mutants provide an excellent new model for studies of HPS5 function. Additionally, the red tilapia mutants may also have potential to serve as new germplasm for aquaculture, or function as a gene resource for genetic modification and breeding of red tilapia and the other related ornamental and food fish in aquaculture. More importantly, this study may have significant values in the area of development and evolution of pigmentation patterns of fish species.
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Mutation of mpv17 results in loss of iridophores due to mitochondrial dysfunction in tilapia
Abstract 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.
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- Award ID(s):
- 1830753
- PAR ID:
- 10655167
- Editor(s):
- Ostrander, Elaine
- Publisher / Repository:
- Oxford
- Date Published:
- Journal Name:
- Journal of Heredity
- Volume:
- 116
- Issue:
- 2
- ISSN:
- 0022-1503
- Page Range / eLocation ID:
- 101 to 112
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1093/jhered/esae034
