Heart defects in X-linked heterotaxy: evidence for a genetic interaction of Zic3 with the nodal signaling pathway

Dev Dyn. 2006 Jun;235(6):1631-7. doi: 10.1002/dvdy.20719.

Abstract

The complex cardiac defects that occur in heterotaxy result from abnormal left-right patterning. Mutations in the zinc finger transcription factor ZIC3 cause X-linked heterotaxy, HTX1. We previously have generated a targeted deletion of the murine Zic3 locus and demonstrated that these knockout mice correctly model HTX1. Fifty percent of Zic3 null embryos have cardiac looping anomalies at embryonic day 10.5 to 14.5, with ventral looping and sinistral looping as the predominant phenotypes. The penetrance of these phenotypes is increased in mice that are also haploinsufficient for Nodal. Zic3(+/-); Nodal (+/-) compound heterozygous mice are born in significantly reduced numbers (P=0.0001), indicating a genetic interaction between the loci. Furthermore, an upstream Nodal enhancer is responsive to Zic3 in both Xenopus and mouse. These studies provide evidence that Zic3 interacts genetically with Nodal in left-right patterning and subsequent cardiac development and delineate a critical Zic3-responsive enhancer required for mediating Nodal expression at the node.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Enhancer Elements, Genetic
  • Genetic Diseases, X-Linked*
  • Heart / embryology
  • Heart Defects, Congenital / genetics*
  • Homeodomain Proteins / genetics*
  • Mice
  • Mice, Inbred C57BL
  • Nodal Protein
  • Signal Transduction / genetics
  • Signal Transduction / physiology*
  • Transcription Factors / deficiency
  • Transcription Factors / genetics*
  • Transforming Growth Factor beta / deficiency
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / physiology*

Substances

  • Homeodomain Proteins
  • Nodal Protein
  • Nodal protein, mouse
  • Transcription Factors
  • Transforming Growth Factor beta
  • Zic3 protein, mouse