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Aberrant cell cycle checkpoint function and early embryonic death in Chk1(-/-) mice.

The recent discovery of checkpoint kinases has suggested the conservation of checkpoint mechanisms between yeast and mammals. In yeast, the protein kinase Chk1 is thought to mediate signaling associated with the DNA damage checkpoint of the cell cycle. However, the function of Chk1 in mammals has remained unknown. Targeted disruption of Chk1 in mice showed that Chk1(-/-) embryos exhibit gross morphologic abnormalities in nuclei as early as the blastocyst stage. In culture, Chk1(-/-) blastocysts showed a severe defect in outgrowth of the inner cell mass and died of apoptosis. DNA replication block and DNA damage failed to arrest the cell cycle before initiation of mitosis in Chk1(-/-) embryos. These results may indicate that Chk1 is indispensable for cell proliferation and survival through maintaining the G(2) checkpoint in mammals.

Pubmed ID: 10859163

Authors

  • Takai H
  • Tominaga K
  • Motoyama N
  • Minamishima YA
  • Nagahama H
  • Tsukiyama T
  • Ikeda K
  • Nakayama K
  • Nakanishi M
  • Nakayama K

Journal

Genes & development

Publication Data

June 15, 2000

Associated Grants

None

Mesh Terms

  • Alleles
  • Animals
  • Animals, Newborn
  • Apoptosis
  • Blastocyst
  • Cell Division
  • Cell Nucleus
  • Cells, Cultured
  • Crosses, Genetic
  • DNA
  • DNA Damage
  • Embryo, Mammalian
  • Fibroblasts
  • G2 Phase
  • Genotype
  • Humans
  • Immunoblotting
  • Immunohistochemistry
  • In Situ Nick-End Labeling
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred ICR
  • Mice, Transgenic
  • Models, Genetic
  • Mutagenesis
  • Protein Kinases
  • Stem Cells