Bone and haematopoietic defects in mice lacking c-fos

Nature. 1992 Dec;360(6406):741-5. doi: 10.1038/360741a0.

Abstract

The proto-oncogene c-fos is the cellular homologue of v-fos originally isolated from murine osteosarcoma. Fos protein is a major component of the AP-1 transcription factor complex, which includes members of the jun family. Stable expression of c-fos in mice has been demonstrated in developing bones and teeth, haematopoietic cells, germ cells and in the central nervous system. It has been proposed that c-fos has an important role in signal transduction, cell proliferation and differentiation. We have previously demonstrated that overexpression of c-fos in transgenic and chimaeric mice specifically affects bone, cartilage and haematopoietic cell development. To understand better the function of c-fos in vivo, we used gene targeting in embryonic stem cells to generate cells and mice lacking c-fos. Here we report that heterozygous fos +/- mice appear normal, although females exhibit a distorted transmission frequency. All homozygous fos -/- mice are growth-retarded, develop osteopetrosis with deficiencies in bone remodelling and tooth eruption, and have altered haematopoiesis. These data define the c-Fos protein as an essential molecule for the development of specific cellular compartments.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B-Lymphocytes / pathology
  • Bone Development / genetics
  • Bone and Bones / abnormalities*
  • Female
  • Gene Deletion*
  • Genes, fos / genetics
  • Genes, fos / physiology*
  • Hematopoiesis / genetics*
  • Heterozygote
  • Homozygote
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Osteopetrosis / genetics
  • Osteopetrosis / pathology
  • Restriction Mapping
  • Spleen / pathology
  • T-Lymphocytes / pathology
  • Thymus Gland / pathology
  • Tooth Eruption / genetics