PUBLICATION
New insights into the all-testis differentiation in zebrafish with compromised endogenous androgen and estrogen synthesis
- Authors
- Ruan, Y., Li, X., Wang, X., Zhai, G., Lou, Q., Jin, X., He, J., Mei, J., Xiao, W., Gui, J., Yin, Z.
- ID
- ZDB-PUB-240308-5
- Date
- 2024
- Source
- PLoS Genetics 20: e1011170e1011170 (Journal)
- Registered Authors
- Mei, Jie, Xiao, Wuhan, Yin, Zhan, Zhai, Gang
- Keywords
- none
- MeSH Terms
-
- Androgens/genetics
- Androgens/metabolism
- Animals
- Estrogens/genetics
- Female
- Gonads/metabolism
- Male
- Sex Differentiation/genetics
- Testis*/metabolism
- Zebrafish*/genetics
- PubMed
- 38451917 Full text @ PLoS Genet.
Citation
Ruan, Y., Li, X., Wang, X., Zhai, G., Lou, Q., Jin, X., He, J., Mei, J., Xiao, W., Gui, J., Yin, Z. (2024) New insights into the all-testis differentiation in zebrafish with compromised endogenous androgen and estrogen synthesis. PLoS Genetics. 20:e1011170e1011170.
Abstract
The regulatory mechanism of gonadal sex differentiation, which is complex and regulated by multiple factors, remains poorly understood in teleosts. Recently, we have shown that compromised androgen and estrogen synthesis with increased progestin leads to all-male differentiation with proper testis development and spermatogenesis in cytochrome P450 17a1 (cyp17a1)-/- zebrafish. In the present study, the phenotypes of female-biased sex ratio were positively correlated with higher Fanconi anemia complementation group L (fancl) expression in the gonads of doublesex and mab-3 related transcription factor 1 (dmrt1)-/- and cyp17a1-/-;dmrt1-/- fish. The additional depletion of fancl in cyp17a1-/-;dmrt1-/- zebrafish reversed the gonadal sex differentiation from all-ovary to all-testis (in cyp17a1-/-;dmrt1-/-;fancl-/- fish). Luciferase assay revealed a synergistic inhibitory effect of Dmrt1 and androgen signaling on fancl transcription. Furthermore, an interaction between Fancl and the apoptotic factor Tumour protein p53 (Tp53) was found in vitro. The interaction between Fancl and Tp53 was observed via the WD repeat domain (WDR) and C-terminal domain (CTD) of Fancl and the DNA binding domain (DBD) of Tp53, leading to the K48-linked polyubiquitination degradation of Tp53 activated by the ubiquitin ligase, Fancl. Our results show that testis fate in cyp17a1-/- fish is determined by Dmrt1, which is thought to stabilize Tp53 by inhibiting fancl transcription during the critical stage of sexual fate determination in zebrafish.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping