Abnormalities of developmental cell death in Dad1-deficient mice

Genes Cells. 1999 Apr;4(4):243-52. doi: 10.1046/j.1365-2443.1999.00256.x.

Abstract

Background: Dad1, the defender against apoptotic cell death, comprises the oligosaccharyltransferase complex and is well conserved among eukaryotes. In hamster BHK21-derived tsBN7 cells, loss of Dad1 causes apoptosis which cannot be prevented by Bcl-2.

Results: To determine the role of Dad1 function in vivo, we prepared by gene targeting, mice harbouring a disrupted Dad1 gene. Homozygous mutants died shortly after they were implanted with the characteristic features of apoptosis. In an in vitro blastocyst culture system, Dad1-null cells displayed abnormalities which were comparable to those obtained in vivo. However, oligosaccharyltransferase activity was apparently retained even after the Dad1-null cells were destined to die. Some live-born heterozygous mutants displayed soft-tissue syndactyly. Mild thymic hypoplasia was also indicated in heterozygotes.

Conclusion: These results suggest the involvement of the Dad1 gene in the acquisition of a common syndactyly phenotype, as well as in the control of programmed cell death during development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis Regulatory Proteins
  • Apoptosis*
  • Blastocyst / physiology*
  • Cells, Cultured
  • Crosses, Genetic
  • Embryonic and Fetal Development*
  • Extremities / embryology
  • Female
  • Gene Deletion
  • Gene Targeting
  • Hexosyltransferases*
  • Male
  • Membrane Proteins / deficiency
  • Membrane Proteins / genetics*
  • Membrane Proteins / physiology*
  • Mice
  • Syndactyly / genetics*
  • Thymus Gland / pathology
  • Transferases / metabolism

Substances

  • Apoptosis Regulatory Proteins
  • Dad1 protein, mouse
  • Membrane Proteins
  • Transferases
  • Hexosyltransferases
  • dolichyl-diphosphooligosaccharide - protein glycotransferase