Identification and Functional Analysis of foxo Genes in Chinese Tongue Sole (Cynoglossus semilaevis)

Int J Mol Sci. 2023 Apr 21;24(8):7625. doi: 10.3390/ijms24087625.

Abstract

The Chinese tongue sole (Cynoglossus semilaevis) is a traditional, precious fish in China. Due to the large growth difference between males and females, the investigation of their sex determination and differentiation mechanisms receives a great deal of attention. Forkhead Box O (FoxO) plays versatile roles in the regulation of sex differentiation and reproduction. Our recent transcriptomic analysis has shown that foxo genes may participate in the male differentiation and spermatogenesis of Chinese tongue sole. In this study, six Csfoxo members (Csfoxo1a, Csfoxo3a, Csfoxo3b, Csfoxo4, Csfoxo6-like, and Csfoxo1a-like) were identified. Phylogenetic analysis indicated that these six members were clustered into four groups corresponding to their denomination. The expression patterns of the gonads at different developmental stages were further analyzed. All members showed high levels of expression in the early stages (before 6 months post-hatching), and this expression was male-biased. In addition, promoter analysis found that the addition of C/EBPα and c-Jun transcription factors enhanced the transcriptional activities of Csfoxo1a, Csfoxo3a, Csfoxo3b, and Csfoxo4. The siRNA-mediated knockdown of the Csfoxo1a, Csfoxo3a, and Csfoxo3b genes in the testicular cell line of Chinese tongue sole affected the expression of genes related to sex differentiation and spermatogenesis. These results have broadened the understanding of foxo's function and provide valuable data for studying the male differentiation of tongue sole.

Keywords: Cynoglossus semilaevis; foxo; promoter activity; siRNA knockdown.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Female
  • Fish Proteins / genetics
  • Fish Proteins / metabolism
  • Flatfishes* / genetics
  • Flatfishes* / metabolism
  • Flounder* / genetics
  • Male
  • Phylogeny
  • Testis / metabolism

Substances

  • Fish Proteins

Grants and funding

This work was funded by National Key R&D Program of China (2022YFD2400405), the National Natural Science Foundation (32072295), Shandong Key R&D Program (For Academician team in Shandong, 2023ZLYS02), and Taishan Scholar Climbing Project Fund of Shandong, China.