4.7 Article

Profile of gene expression changes during estrodio1-17β-induced feminization in the Takifugu rubripes brain

Journal

BMC GENOMICS
Volume 22, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12864-021-08158-0

Keywords

Takifugu rubripes; Brain; Estradiol-17 beta; Sex differentiation; Transcriptome analysis

Funding

  1. Youth Program of National Natural Science Foundation of China [31902347]
  2. General Project of Education Department of Liaoning Province [JL201904]
  3. Projects for Dalian Youth Star of Science and Technology [2019RQ130]
  4. Scientific, Technological and Innovation Program of Dalian [2018J12SN069]
  5. R&D Program of Liaoning Province [2019JH2/10200015]

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The study compared the differential transcriptomic responses of the Takifugu rubripes larvae brain after E-2 treatment, revealing numerous differentially expressed genes and enriched metabolic pathways and signaling pathways. This provides important clues for further research on the possible involvement of the brain-pituitary-gonadal axis network in sex differentiation in T. rubripes.
Background: As the critical tissue of the central nervous system, the brain has been found to be involved in gonad development. Previous studies have suggested that gonadal fate may be affected by the brain. Identifying brain-specific molecular changes that occur during estrodiol-17 beta (E-2)-induced feminization is crucial to our understanding of the molecular control of sex differentiation by the brains of fish. Results: In this study, the differential transcriptomic responses of the Takifugu rubripes larvae brain were compared after E-2 treatment for 55 days. Our results showed that 514 genes were differentially expressed between E-2-treated-XX (E-XX) and Control-XX (C-XX) T. rubripes, while 362 genes were differentially expressed between E-2-treated-XY (E-XY) and Control-XY (C-XY). For example, the expression of cyp19a1b, gnrh1 and pgr was significantly up-regulated, while sr, sl, tsh beta, prl and pit-1, which belong to the growth hormone/prolactin family, were significantly down-regulated after E-2 treatment, in both sexes. The arntl1, bhlbe, nr1d2, per1b, per3, cry1, cipc and ciart genes, which are involved in the circadian rhythm, were also found to be altered. Differentially expressed genes (DEGs), which were identified between E-XX and C-XX, were significantly enriched in neuroactive ligand-receptor interaction, arachidonic acid metabolism, cytokine-cytokine receptor interaction and the calcium signaling pathway. The DEGs that were identified between E-XY and C-XY were significantly enriched in tyrosine metabolism, phenylalanine metabolism, arachidonic acid metabolism and linoleic acid metabolism. Conclusion: A number of genes and pathways were identified in the brain of E-2-treated T. rubripes larvae by RNA-seq. It provided the opportunity for further study on the possible involvement of networks in the brain-pituitary-gonadal axis in sex differentiation in T. rubripes.

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