Characterization of gonadal transcriptomes from Nile tilapia (Oreochromis niloticus) reveals differentially expressed genes

PLoS One. 2013 May 3;8(5):e63604. doi: 10.1371/journal.pone.0063604. Print 2013.

Abstract

Four pairs of XX and XY gonads from Nile tilapia were sequenced at four developmental stages, 5, 30, 90, and 180 days after hatching (dah) using Illumina Hiseq(TM) technology. This produced 28 Gb sequences, which were mapped to 21,334 genes. Of these, 259 genes were found to be specifically expressed in XY gonads, and 69 were found to be specific to XX gonads. Totally, 187 XX- and 1,358 XY-enhanced genes were identified, and 2,978 genes were found to be co-expressed in XX and XY gonads. Almost all steroidogenic enzymes, including cyp19a1a, were up-regulated in XX gonads at 5 dah; but in XY gonads these enzymes, including cyp11b2, were significantly up-regulated at 90 dah, indicating that, at a time critical to sex determination, the XX fish produced estrogen and the XY fish did not produce androgens. The most pronounced expression of steroidogenic enzyme genes was observed at 30 and 90 dah for XX and XY gonads, corresponding to the initiation of germ cell meiosis in the female and male gonads, respectively. Both estrogen and androgen receptors were found to be expressed in XX gonads, but only estrogen receptors were expressed in XY gonads at 5 dah. This could explain why exogenous steroid treatment induced XX and XY sex reversal. The XX-enhanced expression of cyp19a1a and cyp19a1b at all stages suggests an important role for estrogen in female sex determination and maintenance of phenotypic sex. This work is the largest collection of gonadal transcriptome data in tilapia and lays the foundation for future studies into the molecular mechanisms of sex determination and maintenance of phenotypic sex in non-model teleosts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Androgens / genetics
  • Androgens / metabolism
  • Animals
  • Cichlids / genetics*
  • Cichlids / growth & development
  • Estrogens / genetics
  • Estrogens / metabolism
  • Female
  • Fish Proteins / genetics*
  • Fish Proteins / metabolism
  • Gene Expression Regulation, Developmental*
  • Germ Cells / cytology
  • Germ Cells / growth & development
  • Germ Cells / metabolism
  • Gonads / growth & development
  • Gonads / metabolism*
  • Life Cycle Stages / genetics*
  • Male
  • Receptors, Androgen / genetics
  • Receptors, Androgen / metabolism
  • Receptors, Estrogen / genetics
  • Receptors, Estrogen / metabolism
  • Sequence Analysis, DNA
  • Sex Differentiation
  • Transcriptome*

Substances

  • Androgens
  • Estrogens
  • Fish Proteins
  • Receptors, Androgen
  • Receptors, Estrogen

Grants and funding

This work was supported by grants 31030063 and 30871905 from the National Natural Science Foundation of China; the NSFC-RGC Joint Research Scheme from the National Science Foundation of China (NSFC:30831160508); grants 2009CB941200, 2010CB134405, and 2012CB723205 from the National Basic Research Program of China; grant 2011AA100404 from the National High Technology Research and Development Program (863 program) of China; grant IRT0859 from the Program for Changjiang Scholars and Innovative Research Team in University; grant 20090182110008 from the Specialized Research Fund for the Doctoral Program of Higher Education of China; grants CQ CSTC 2008BB1006 and 2008AC1016 from the Natural Science Foundation Project of Chongqing, Chongqing Science and Technology Commission, and grants kb2010009 and kb2011007 from the Excellent Ph.D Thesis Fellowship of Southwest University. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.