• Register
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.


Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.


The Hectd1 ubiquitin ligase is required for development of the head mesenchyme and neural tube closure.

Closure of the cranial neural tube depends on normal development of the head mesenchyme. Homozygous-mutant embryos for the ENU-induced open mind (opm) mutation exhibit exencephaly associated with defects in head mesenchyme development and dorsal-lateral hinge point formation. The head mesenchyme in opm mutant embryos is denser than in wildtype embryos and displays an abnormal cellular organization. Since cells that originate from both the cephalic paraxial mesoderm and the neural crest populate the head mesenchyme, we explored the origin of the abnormal head mesenchyme. opm mutant embryos show apparently normal development of neural crest-derived structures. Furthermore, the abnormal head mesenchyme in opm mutant embryos is not derived from the neural crest, but instead expresses molecular markers of cephalic mesoderm. We also report the identification of the opm mutation in the ubiquitously expressed Hectd1 E3 ubiquitin ligase. Two different Hectd1 alleles cause incompletely penetrant neural tube defects in heterozygous animals, indicating that Hectd1 function is required at a critical threshold for neural tube closure. This low penetrance of neural tube defects in embryos heterozygous for Hectd1 mutations suggests that Hectd1 should be considered as candidate susceptibility gene in human neural tube defects.

Pubmed ID: 17442300


  • Zohn IE
  • Anderson KV
  • Niswander L


Developmental biology

Publication Data

June 1, 2007

Associated Grants

  • Agency: NICHD NIH HHS, Id: F32 HD008605
  • Agency: NICHD NIH HHS, Id: F32 HD008605-04
  • Agency: NICHD NIH HHS, Id: F32-HD08605
  • Agency: NICHD NIH HHS, Id: R01 HD035455
  • Agency: NICHD NIH HHS, Id: R01 HD035455-05
  • Agency: NICHD NIH HHS, Id: R01-HD035455
  • Agency: NICHD NIH HHS, Id: U01 HD043478
  • Agency: NICHD NIH HHS, Id: U01 HD043478-05
  • Agency: NICHD NIH HHS, Id: U01-HD43478

Mesh Terms

  • Alleles
  • Animals
  • Biological Markers
  • Central Nervous System
  • Embryo, Mammalian
  • Embryonic Development
  • Gene Expression
  • Mesoderm
  • Mice
  • Mice, Mutant Strains
  • Mutation
  • Neural Tube Defects
  • Protein Structure, Tertiary
  • Skull
  • Ubiquitin-Protein Ligases