Participation of androgen and its receptor in sex determination of an amphibian species

PLoS One. 2017 Jun 5;12(6):e0178067. doi: 10.1371/journal.pone.0178067. eCollection 2017.

Abstract

Introduction: In the Japanese frog Rana (R.) rugosa the androgen receptor (AR) gene on the W chromosome (W-AR) is barely expressed. Previously we showed that incomplete female-to-male sex-reversal occurred in Z-AR transgenic female frogs. To date, however, there is no report showing that AR with androgens can determine genetically programed male sex fate in any vertebrate species. Here, we examined whether AR together with androgens functions as a sex determinant in an amphibian species.

Methods: To examine whether complete female-to-male sex-reversal occurs in R. rugosa frogs, we produced AR-transgenic (Tg) and -knockdown (KD) female R. rugosa frogs by the I-SceI meganuclease-mediated gene trap and CRISPR/Cas9 system, respectively. AR-Tg and -KD tadpoles were reared in water containing testosterone (T) at 0 to 7.1 ng/ml. Frozen sections were prepared from the gonads of metamorphosed frogs and immunostained for laminin, Vasa, Pat1a, CYP17 and AR. We also employed PCR analysis to examine Dmrt1, Pat1a and CYP17 expression in the gonads of KD and placebo-KD female frogs.

Results: Complete female-to-male sex-reversal occurred in the AR-Tg ZW female frogs when a low dosage of T was supplied in the rearing water of tadpoles. However, no sex-reversal was observed in AR-KD ZW female frogs when the gonads were treated with dosages of T high enough to induce complete female-to-male sex-reversal even in wild type frogs.

Discussion: These results suggest that AR with its androgen ligand functions as a male sex-determinant in the ZW type R. rugosa frogs.

MeSH terms

  • Amphibian Proteins / genetics
  • Amphibian Proteins / metabolism
  • Animals
  • Animals, Genetically Modified
  • Base Sequence
  • CRISPR-Cas Systems
  • DEAD-box RNA Helicases / genetics
  • DEAD-box RNA Helicases / metabolism
  • Deoxyribonucleases, Type II Site-Specific / genetics
  • Deoxyribonucleases, Type II Site-Specific / metabolism
  • Female
  • Gene Editing
  • Gene Expression Regulation, Developmental*
  • Gene Knockdown Techniques
  • Laminin / genetics
  • Laminin / metabolism
  • Larva / drug effects
  • Larva / genetics
  • Larva / growth & development
  • Larva / metabolism
  • Male
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • Ranidae / genetics*
  • Ranidae / growth & development
  • Ranidae / metabolism
  • Receptors, Androgen / deficiency
  • Receptors, Androgen / genetics*
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism
  • Sex Chromosomes / chemistry
  • Sex Chromosomes / drug effects*
  • Sex Chromosomes / metabolism
  • Sex Determination Analysis
  • Sex Determination Processes*
  • Steroid 17-alpha-Hydroxylase / genetics
  • Steroid 17-alpha-Hydroxylase / metabolism
  • Testosterone / metabolism
  • Testosterone / pharmacology*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • Amphibian Proteins
  • DMRT1 protein
  • Laminin
  • Receptors, Androgen
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors
  • Testosterone
  • Steroid 17-alpha-Hydroxylase
  • Protein Serine-Threonine Kinases
  • SCEI protein, S cerevisiae
  • Deoxyribonucleases, Type II Site-Specific
  • DEAD-box RNA Helicases