ZFIN ID: ZDB-PUB-041022-7
Zebrafish IRX1b in the embryonic cardiac ventricle
Joseph, E.M.
Date: 2004
Source: Developmental dynamics : an official publication of the American Association of Anatomists   231(4): 720-726 (Journal)
Registered Authors: Joseph, Elaine
Keywords: none
MeSH Terms:
  • Animals
  • Embryo, Nonmammalian/embryology
  • Embryo, Nonmammalian/physiology
  • Endothelin Receptor Antagonists
  • Gene Expression Regulation, Developmental
  • Heart/embryology*
  • Heart/physiology*
  • Heart Conduction System/cytology
  • Heart Conduction System/embryology
  • Heart Conduction System/physiology
  • Heart Ventricles/cytology
  • Heart Ventricles/embryology
  • Homeodomain Proteins/genetics*
  • Sulfonamides/pharmacology
  • Transcription Factors/genetics*
  • Ventricular Function
  • Zebrafish/embryology*
  • Zebrafish/physiology
  • Zebrafish Proteins
PubMed: 15497138 Full text @ Dev. Dyn.
The synchronous contraction of the vertebrate heart requires a conduction system. While coordinated contraction of the cardiac chambers is observed in zebrafish larvae, no histological evidence yet has been found for the existence of a cardiac conduction system in this tractable teleost. The homeodomain transcription factor gene IRX1 has been shown in the mouse embryo to be a marker of cells that give rise to the distinctive cardiac ventricular conduction system. Here, I demonstrate that zebrafish IRX1b is expressed in a restricted subset of ventricular myocytes within the embryonic zebrafish heart. IRX1b expression occurs as the electrical maturation of the heart is taking place, in a location analogous to the initial expression domain of mouse IRX1. The gene expression pattern of IRX1b is altered in silent heart genetic mutant embryos and in embryos treated with the endothelin receptor antagonist bosentan. Furthermore, injection of a morpholino oligonucleotide targeted to block IRX1b translation slows the heart rate. Developmental Dynamics, 2004. (c) 2004 Wiley-Liss, Inc.