
The murine severe combined immunodeficiency (scid) mutation interferes with normal recombination of immunoglobulin and T-cell receptor genes. This immunologic defect results in a lack of fully differentiated B and T cells in scid/scid mice. Animals homozygous for the scid mutation also display increased sensitivity to the damaging effects of ionizing radiation. We report here our observations of high frequencies of radiation-induced chromatid interchanges and intrachanges in bone marrow cells and fibroblasts from scid/scid mice. The presence of these aberrant chromosome structures suggests that a delay in strand rejoining underlies the increased sensitivity of scid/scid mice to ionizing radiation. The scid mutation may provide important clues for understanding the relationship between mitotic recombination and DNA repair in higher eukaryotic cells.
Chromosome Aberrations, DNA-Repair, 570, DNA Repair, 610, Dose-Response Relationship, Radiation, Mice, SCID, Gamma-Rays, Chromosomes, Mice-SCID: ge, Mice, Mutation: ge, Chromosomes: re, Gamma Rays, Cells-Cultured, SUPPORT-U-S-GOVT-P-H-S, Mutation, Animals, Dose-Response-Relationship-Radiation, Cells, Cultured, Chromosome-Aberrations
Chromosome Aberrations, DNA-Repair, 570, DNA Repair, 610, Dose-Response Relationship, Radiation, Mice, SCID, Gamma-Rays, Chromosomes, Mice-SCID: ge, Mice, Mutation: ge, Chromosomes: re, Gamma Rays, Cells-Cultured, SUPPORT-U-S-GOVT-P-H-S, Mutation, Animals, Dose-Response-Relationship-Radiation, Cells, Cultured, Chromosome-Aberrations
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