Posterior transformation, neurological abnormalities, and severe hematopoietic defects in mice with a targeted deletion of the bmi-1 proto-oncogene

Genes Dev. 1994 Apr 1;8(7):757-69. doi: 10.1101/gad.8.7.757.

Abstract

The bmi-1 proto-oncogene has been implicated in B-cell lymphomagenesis in E mu-myc transgenic mice. Distinct domains of the Bmi-1 protein are highly conserved within the Drosophila protein Posterior Sex Combs, a member of the Polycomb group involved in maintaining stable repression of homeotic genes during development. We have inactivated the bmi-1 gene in the germ line of mice by homologous recombination in ES cells. Null mutant mice display three phenotypic alterations: (1) a progressive decrease in the number of hematopoietic cells and an impaired proliferative response of these cells to mitogens; (2) neurological abnormalities manifested by an ataxic gait and sporadic seizures; and (3) posterior transformation, in most cases along the complete anteroposterior axis of the skeleton. The observations indicate that Mbi-1 plays an important role in morphogenesis during embryonic development and in hematopoiesis throughout pre- and postnatal life. Furthermore, these data provide the first evidence of functional conservation of a mammalian Polycomb group homolog.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Ataxia / genetics
  • Bone Marrow Cells
  • Brain / abnormalities*
  • Embryonic and Fetal Development
  • Female
  • Gene Expression Regulation, Developmental
  • Gene Targeting
  • Germ-Line Mutation / physiology
  • Hematopoietic System / abnormalities*
  • Hematopoietic System / cytology
  • Lymphocyte Activation
  • Male
  • Mice
  • Mice, Transgenic
  • Mitogens / pharmacology
  • Nuclear Proteins / genetics
  • Nuclear Proteins / physiology*
  • Polycomb Repressive Complex 1
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / physiology*
  • Proto-Oncogenes
  • Recombination, Genetic
  • Repressor Proteins*
  • Ribs / abnormalities
  • Seizures / genetics
  • Spine / abnormalities*
  • Spleen / cytology
  • Thymus Gland / cytology

Substances

  • Bmi1 protein, mouse
  • Mitogens
  • Nuclear Proteins
  • Proto-Oncogene Proteins
  • Repressor Proteins
  • Polycomb Repressive Complex 1