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Germ cell defects and hematopoietic hypersensitivity to gamma-interferon in mice with a targeted disruption of the Fanconi anemia C gene.

Blood | Jul 1, 1996

http://www.ncbi.nlm.nih.gov/pubmed/8704201

Fanconi anemia (FA) is an autosomal recessive chromosome instability syndrome characterized by progressive bone marrow (BM) failure, skeletal defects, and increased susceptibility to malignancy. FA cells are hypersensitive to DNA cross-linking agents, oxygen and have cell cycle abnormalities. To develop an animal model of the disease we generated mice homozygous for a targeted deletion of exon 9 of the murine FA complementation group C gene (fac). Mutant mice had normal neonatal viability and gross morphology, but their cells had the expected chromosome breakage and DNA cross-linker sensitivity. Surprisingly, male and female mutant mice had reduced numbers of germ cells and females had markedly impaired fertility. No anemia was detectable in the peripheral blood during the first year of life, but the colony forming capacity of marrow progenitor cells was abnormal in vitro in mutant mice. Progenitor cells from fac knock-out mice were hypersensitive to interferon gamma. This previously unrecognized phenotype may form the basis for BM failure in human FA.

Pubmed ID: 8704201 RIS Download

Mesh terms: Animals | Base Sequence | Cell Cycle | Cell Cycle Proteins | Cells, Cultured | Chemokine CCL4 | Chromosome Aberrations | Colony-Forming Units Assay | Cross-Linking Reagents | DNA Damage | DNA-Binding Proteins | Exons | Fanconi Anemia | Fanconi Anemia Complementation Group C Protein | Fanconi Anemia Complementation Group Proteins | Female | Germ Cells | Hematopoietic Cell Growth Factors | Hematopoietic Stem Cells | Infertility, Female | Interferon-gamma | Macrophage Inflammatory Proteins | Male | Mice | Mice, Inbred C57BL | Mice, Knockout | Molecular Sequence Data | Monokines | Nuclear Proteins | Ovary | Proteins | Recombinant Proteins | Single-Blind Method | Testis | Tumor Necrosis Factor-alpha

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Associated grants

  • Agency: NHLBI NIH HHS, Id: 1PO1HL48546
  • Agency: NCI NIH HHS, Id: CA36306
  • Agency: NHLBI NIH HHS, Id: HL48546

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