ZFIN ID: ZDB-PUB-170215-4
Sequential, Divergent and Cooperative Requirements of Foxl2a and Foxl2b in Ovary Development and Maintenance of Zebrafish
Yang, Y.J., Wang, Y., Li, Z., Zhou, L., Gui, J.F.
Date: 2017
Source: Genetics 205(4): 1551-1572 (Journal)
Registered Authors: Gui, Jian-Fang, Li, Zhi, Wang, Yang, Zhou, Li
Keywords: Foxl2a, Foxl2b, TALEN, premature ovarian failure, sex reversal
MeSH Terms:
  • Animals
  • Aromatase/genetics
  • Aromatase/metabolism
  • Female
  • Forkhead Transcription Factors/genetics*
  • Forkhead Transcription Factors/metabolism
  • Homozygote
  • Male
  • Mutation
  • Oogenesis
  • Ovary/growth & development
  • Ovary/metabolism*
  • SOX9 Transcription Factor/genetics
  • SOX9 Transcription Factor/metabolism
  • Sex Determination Processes*
  • Transcription Factors/genetics
  • Transcription Factors/metabolism
  • Zebrafish/genetics*
  • Zebrafish/growth & development
  • Zebrafish/metabolism
  • Zebrafish Proteins/genetics*
  • Zebrafish Proteins/metabolism
PubMed: 28193729 Full text @ Genetics
Foxl2 is essential for mammalian ovary maintenance. Although sexually dimorphic expression of foxl2 was observed in many teleost, its role and regulative mechanism in fish remained largely unclear. In this study, we first identified two transcript variants of foxl2a and its homologous gene foxl2b in zebrafish, and revealed their specific expression in follicular layer cells in a sequential and divergent fashion during ovary differentiation, maturation and maintenance. Then, homozygous foxl2a mutants (foxl2a(-/-)) and foxl2b mutants (foxl2b(-/-)) were constructed, and detailed comparisons, such as sex ratio, gonadal histological structure, transcriptome profiling and dynamic expression of gonadal development-related genes, were carried out. Initial ovarian differentiation and oocyte development occur normally both in foxl2a(-/-) and foxl2b(-/-) mutants, but foxl2a and foxl2b disruptions result in premature ovarian failure and partial sex reversal in adult females respectively. In foxl2a(-/-) female mutants, sox9a-amh/cyp19a1a signaling was up-regulated at 150 day post fertilization (dpf) and subsequently triggers oocyte apoptosis after 180 dpf. In contrast, dmrt1 expression was greater at 105 dpf and increased several hundred fold in foxl2b(-/-) mutated ovaries at 270 dpf, along with other testis-related genes. Finally, homozygous foxl2a(-/-)/foxl2b(-/-) double mutants were constructed, in which complete sex reversal occurs early and testis-differentiation genes robustly increase at 60 dpf. Given mutual compensation between foxl2a and foxl2b in foxl2b(-/-) and foxl2a(-/-) mutants, we proposed a model, in which foxl2a and foxl2b cooperate to regulate zebrafish ovary development and maintenance, with foxl2b potentially having a dominant role in preventing the ovary from differentiating as testis, as compared to foxl2a.