ZFIN ID: ZDB-PUB-070330-40
Anti-Mullerian hormone and 11 beta-hydroxylase show reciprocal expression to that of aromatase in the transforming gonad of zebrafish males
Wang, X.G., and Orban, L.
Date: 2007
Source: Developmental dynamics : an official publication of the American Association of Anatomists   236(5): 1329-1338 (Journal)
Registered Authors: Orban, Laszlo, Wang, Xingang
Keywords: zebrafish sex, juvenile hermaphrodite, Leydig cell, Sertoli cell, Müllerian inhibiting substance, steroidgenesis, hormone balance
MeSH Terms:
  • Amino Acid Sequence
  • Animals
  • Animals, Genetically Modified
  • Anti-Mullerian Hormone
  • Aromatase/genetics*
  • Female
  • Gene Expression Regulation, Developmental
  • Glycoproteins/genetics*
  • Green Fluorescent Proteins/genetics
  • In Situ Hybridization
  • Male
  • Molecular Sequence Data
  • Ovary/embryology
  • Ovary/growth & development
  • Ovary/metabolism
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • Sequence Homology, Amino Acid
  • Sex Characteristics
  • Sex Differentiation/genetics
  • Signal Transduction
  • Steroid 11-beta-Hydroxylase/genetics*
  • Testicular Hormones/genetics*
  • Testis/embryology
  • Testis/growth & development
  • Testis/metabolism
  • Testosterone/analogs & derivatives
  • Testosterone/metabolism
  • Zebrafish/embryology*
  • Zebrafish/genetics*
  • Zebrafish/growth & development
  • Zebrafish/metabolism
  • Zebrafish Proteins/genetics
PubMed: 17393497 Full text @ Dev. Dyn.
FIGURES
ABSTRACT
During development all zebrafish males first develop a "juvenile ovary" that later degenerates and transforms into a testis. In this study, individuals undergoing gonadal transformation were identified from a vas::egfp transgenic line and used for gene expression analysis of anti-Mullerian hormone (amh), ovarian aromatase (cyp19a1a) and 11beta-hydroxylase (cyp11b, also known as P450(11beta)) by real-time polymerase chain reaction and in situ hybridization. In the "normal (i.e., nontransforming) juvenile ovary" cyp19a1a was expressed around the oocytes, but cyp11b and amh could not be detected. During gonadal transformation cyp19a1a was down-regulated and could not be detected anymore; in contrast amh was up-regulated and highly expressed at similar regions where cyp19a1a had been expressed earlier. Furthermore, the normalized transcript levels of cyp19a1a and amh showed a reciprocal picture, i.e., the higher was the level of amh, the lower was that of cyp19a1a. Expression of cyp11b was also up-regulated but later than amh, and its localization was not related to the position of degenerating oocytes. These data indicate that amh is a candidate gene down-regulating cyp19a1a, leading to "juvenile ovary-to-testis" transformation. Whereas, cyp11b or its product, 11-ketotestosterone, is unlikely to be the inducer of zebrafish gonad transformation, as proposed earlier for some protogynous hermaphroditic fish species.
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