Mice with a homozygous gene trap vector insertion in mgcRacGAP die during pre-implantation development

Mech Dev. 2001 Apr;102(1-2):33-44. doi: 10.1016/s0925-4773(01)00279-9.

Abstract

In a phenotypic screen in mice using a gene trap approach in embryonic stem cells, we have identified a recessive loss-of-function mutation in the mgcRacGAP gene. Maternal protein is present in the oocyte, and mgcRacGAP gene transcription starts at the four-cell stage and persists throughout mouse pre-implantation development. Total mgcRacGAP deficiency results in pre-implantation lethality. Such E3.5 embryos display a dramatic reduction in cell number, but undergo compaction and form a blastocoel. At E3.0-3.5, binucleated blastomeres in which the nuclei are partially interconnected are frequently observed, suggesting that mgcRacGAP is required for normal mitosis and cytokinesis in the pre-implantation embryo. All homozygous mutant blastocysts fail to grow out on fibronectin-coated substrates, but a fraction of them can still induce decidual swelling in vivo. The mgcRacGAP mRNA expression pattern in post-implantation embryos and adult mouse brain suggests a role in neuronal cells. Our results indicate that mgcRacGAP is essential for the earliest stages of mouse embryogenesis, and add evidence that CYK-4-like proteins also play a role in microtubule-dependent steps in the cytokinesis of vertebrate cells. In addition, the severe phenotype of null embryos indicates that mgcRacGAP is functionally non-redundant and cannot be substituted by other GAPs during early cleavage of the mammalian embryo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Northern
  • Brain / embryology
  • Brain / metabolism
  • Cell Nucleus / metabolism
  • Cloning, Molecular
  • DNA, Complementary / metabolism
  • Embryo, Mammalian / physiology*
  • Female
  • GTP Phosphohydrolase Activators / metabolism*
  • GTPase-Activating Proteins / genetics*
  • GTPase-Activating Proteins / physiology*
  • Galactosides / metabolism
  • Genotype
  • Heterozygote
  • Homozygote*
  • In Situ Hybridization
  • Indoles / metabolism
  • Male
  • Mice
  • Models, Genetic
  • Mutation
  • Phalloidine / pharmacology
  • Phenotype
  • RNA, Messenger / metabolism
  • Recombinant Fusion Proteins / metabolism
  • Time Factors
  • Tissue Distribution
  • Transcription, Genetic*

Substances

  • DNA, Complementary
  • GTP Phosphohydrolase Activators
  • GTPase-Activating Proteins
  • Galactosides
  • Indoles
  • RNA, Messenger
  • Recombinant Fusion Proteins
  • mgcRacGAP
  • Phalloidine
  • 5-bromo-4-chloro-3-indolyl beta-galactoside