Transcriptome Profiling and Analysis of Genes Associated with High Temperature–Induced Masculinization in Sex-Undifferentiated Nile Tilapia Gonad

Artificially high temperatures during critical thermosensitive periods (TSPs) can induce the sex reversal of Nile tilapia ( Oreochromis niloticus ) females into pseudomales; Nile tilapia is a GSD + TE (genotypic plus temperature effects) fish species. Previous studies have shown that water temperatu...

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Veröffentlicht in:Marine biotechnology (New York, N.Y.) N.Y.), 2020-06, Vol.22 (3), p.367-379
Hauptverfasser: Teng, Jian, Zhao, Yan, Chen, Hong Ju, Wang, Hui, Ji, Xiang Shan
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Sprache:eng
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Zusammenfassung:Artificially high temperatures during critical thermosensitive periods (TSPs) can induce the sex reversal of Nile tilapia ( Oreochromis niloticus ) females into pseudomales; Nile tilapia is a GSD + TE (genotypic plus temperature effects) fish species. Previous studies have shown that water temperature affects the expression levels of many genes in the gonad or brain in various teleost species. However, few studies on the effect of temperature at the whole-gonad transcriptomic level in the early stage of sex differentiation have been reported in fish species exhibiting GSD + TE. In this study, RNA-Seq was performed to characterize the transcriptomic profile and identify genes exhibiting temperature- and sex-biased expressions in the Nile tilapia gonad at 21 dpf. A total of 42 genes were found to be associated with both high-temperature treatment and sex development, as the expression levels of these genes differed in both FC (female control) vs MC (male control) and FC vs FT (high temperature–treated females in the TSP). Among these genes, the transcriptional alterations of many male sex determination and differentiation genes, such as Dmrt1 , Gsdf , and the DNA damage-inducible protein GADD45 alpha, suggested that the male pathway is initiated after high-temperature treatment and that its initiation may play a role in high temperature–induced masculinization in Nile tilapia. The qRT-PCR validation results for thirteen differentially expressed genes showed that the Pearson’s correlation of the log 10 fold change values between the qPCR and RNA-Seq results was 0.70 ( p  
ISSN:1436-2228
1436-2236
DOI:10.1007/s10126-020-09956-5