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      Bone and haematopoietic defects in mice lacking c-fos.

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

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          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.

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