Defective repair of radiation-induced chromosomal damage in scid/scid mice

Cytogenet Cell Genet. 1992;59(1):39-44. doi: 10.1159/000133196.

Abstract

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.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cells, Cultured
  • Chromosome Aberrations*
  • Chromosomes / radiation effects*
  • DNA Repair*
  • Dose-Response Relationship, Radiation
  • Gamma Rays
  • Mice
  • Mice, SCID / genetics*
  • Mutation / genetics