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      Bub3 gene disruption in mice reveals essential mitotic spindle checkpoint function during early embryogenesis.

      Genes & development
      Animals, Cell Cycle Proteins, Chimera, Chromosomal Proteins, Non-Histone, Embryonic and Fetal Development, Mice, Mice, Inbred C57BL, Mitosis, Mutagenesis, Insertional, Nocodazole, pharmacology, Proteins, genetics, metabolism, Spindle Apparatus

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          Abstract

          Bub3 is a conserved component of the mitotic spindle assembly complex. The protein is essential for early development in Bub3 gene-disrupted mice, evident from their failure to survive beyond day 6.5-7.5 postcoitus (pc). Bub3 null embryos appear normal up to day 3.5 pc but accumulate mitotic errors from days 4.5-6.5 pc in the form of micronuclei, chromatin bridging, lagging chromosomes, and irregular nuclear morphology. Null embryos treated with a spindle-depolymerising agent fail to arrest in metaphase and show an increase in mitotic disarray. The results confirm Bub3 as a component of the essential spindle checkpoint pathway that operates during early embryogenesis.

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