Figla Favors Ovarian Differentiation by Antagonizing Spermatogenesis in a Teleosts, Nile Tilapia (Oreochromis niloticus)

PLoS One. 2015 Apr 20;10(4):e0123900. doi: 10.1371/journal.pone.0123900. eCollection 2015.

Abstract

Figla (factor in the germ line, alpha), a female germ cell-specific transcription factor, had been shown to activate genetic hierarchies in oocytes. The ectopic expression of Figla was known to repress spermatogenesis-associated genes in male mice. However, the potential role of Figla in other vertebrates remains elusive. The present work was aimed to identify and characterize the functional relevance of Figla in the ovarian development of Nile tilapia (Oreochromis niloticus). Tissue distribution and ontogeny analysis revealed that tilapia Figla gene was dominantly expressed in the ovary from 30 days after hatching. Immunohistochemistry analysis also demonstrated that Figla was expressed in the cytoplasm of early primary oocytes. Intriguingly, over-expression of Figla in XY fish resulted in the disruption of spermatogenesis along with the depletion of meiotic spermatocytes and spermatids in testis. Dramatic decline of sycp3 (synaptonemal complex protein 3) and prm (protamine) expression indicates that meiotic spermatocytes and mature sperm production are impaired. Even though Sertoli cell (dmrt1) and Leydig cell (star and cyp17a1) marker genes remained unaffected, hsd3b1 expression and 11-KT production were enhanced in Figla-transgene testis. Taken together, our data suggest that fish Figla might play an essential role in the ovarian development by antagonizing spermatogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Androgens
  • Animals
  • Animals, Genetically Modified
  • Base Sequence
  • Cell Differentiation*
  • Cichlids / metabolism*
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental
  • Male
  • Ovary / cytology*
  • Ovary / metabolism
  • Phylogeny
  • Spermatogenesis*
  • Subcellular Fractions / metabolism
  • Synteny / genetics
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transgenes

Substances

  • Androgens
  • Transcription Factors

Grants and funding

This work was supported in part by Grants for Scientific Research from the National Natural Science Foundation of China (31201986, 91331119, 31201979, and 31030063). This work was also supported in part by Research Foundation of Talent Introduction of Southwest University, China (SWU111003). The project was supported by the Specialized Research Fund for the Doctoral Program of Higher Education of China, Ministry of Education (20110182120003 and 20130182130003) and the special fund of Chongqing key laboratory (CSTC), Natural Science Foundation Project of Chongqing, China (cstc2012jjA80005 and cstc2012jjA80041). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.