ZFIN ID: ZDB-PUB-140603-5
Use of antagonists and morpholinos in loss-of-function analyses: estrogen receptor ESR2a mediates the effects of 17alpha-ethinylestradiol on primordial germ cell distribution in zebrafish
Hu, J., Sun, S., Guo, M., Song, H.
Date: 2014
Source: Reproductive Biology and Endocrinolgy   12: 40 (Journal)
Registered Authors: Song, Houyan
Keywords: none
MeSH Terms:
  • 5' Untranslated Regions/drug effects
  • Animals
  • Cell Movement/drug effects
  • Embryonic Development/drug effects
  • Endocrine Disruptors/toxicity*
  • Estrogen Receptor Antagonists/pharmacology*
  • Estrogen Receptor alpha/agonists
  • Estrogen Receptor alpha/antagonists & inhibitors
  • Estrogen Receptor alpha/genetics
  • Estrogen Receptor alpha/metabolism
  • Estrogen Receptor beta/agonists
  • Estrogen Receptor beta/antagonists & inhibitors
  • Estrogen Receptor beta/genetics
  • Estrogen Receptor beta/metabolism
  • Ethinyl Estradiol/toxicity*
  • Fluorescent Dyes/metabolism
  • Genes, Reporter/drug effects
  • Germ Cells/drug effects*
  • Germ Cells/metabolism
  • Green Fluorescent Proteins/genetics
  • Green Fluorescent Proteins/metabolism
  • Microinjections
  • Morpholinos/pharmacology*
  • Receptors, Estrogen/antagonists & inhibitors
  • Receptors, Estrogen/genetics
  • Receptors, Estrogen/metabolism
  • Sexual Development/drug effects
  • Water Pollutants, Chemical/toxicity
  • Zebrafish/embryology*
  • Zebrafish/metabolism
  • Zebrafish Proteins/agonists*
  • Zebrafish Proteins/antagonists & inhibitors
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism
PubMed: 24886565 Full text @ Reprod. Biol. Endocrinol.
Various chemicals released into the aquatic environment adversely affect the reproductive system of fish, particularly by changing gonad structure and function. 17alpha-ethinylestradiol (EE2) is a potent environmental estrogen that disrupts sexual differentiation and normal reproduction in fish. Previous studies have shown that exposure to endocrine-disrupting chemicals (EDCs) disrupts the migration of primordial germ cells (PGCs) in zebrafish.
To investigate the effects of EE2 exposure on PGC migration, zebrafish embryos were injected with gfp-nanos mRNA to label PGCs and subsequently exposed to different concentrations of EE2. Typical estrogen receptor antagonist treatment and morpholino knockdown experiments were used to identify functional estrogen receptors that mediate the effects of EE2.
The migration of PGCs was disrupted after exposure to high concentrations of EE2 (1 mirog/L). Loss-of-function analyses were performed for estrogen receptor ESR1, ESR2a, and ESR2b, and only loss of ESR2a resulted in a decreased number of ectopic PGCs following exposure to 1 mirog/L EE2.
EE2 exposure disrupts PGC migration and distribution, and this effect is mediated through the estrogen receptor ESR2a.