Radiation-induced chromosome aberrations analysed by two-colour fluorescence in situ hybridization with composite whole chromosome-specific DNA probes and a pancentromeric DNA probe

Int J Radiat Biol. 1993 Aug;64(2):179-84. doi: 10.1080/09553009314551271.

Abstract

Fluorescence in situ hybridization with composite whole chromosome-specific DNA probes for human chromosomes 1, 4 and 12 and a degenerate alpha-satellite pancentromeric DNA probe labelled with digoxigenin was used to measure symmetrical translocations and dicentrics induced in vitro by 137Cs gamma-rays (0-6.0 Gy) in peripheral lymphocytes. Despite subtracting our mean background translocation frequency of 0.0016 per cell (11,411 cells scored from 11 individuals) from induced frequencies, about 1.3-1.8-fold more translocations were found than dicentrics at a given dose. Translocation frequencies determined only in stable cells agree well with total translocation frequencies determined also in cells containing additional unstable chromosomal changes. The linear quadratic calibration curve generated for total stable translocations is based on approx. 17,000 cells. The suitability of this curve for biological dosimetry of human radiation exposure can now be evaluated in comparison with dose estimates based on a conventional dicentric dose-response curve.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cesium Radioisotopes
  • Chromosome Aberrations*
  • Chromosomes, Human / radiation effects*
  • Chromosomes, Human, Pair 1 / radiation effects
  • Chromosomes, Human, Pair 12 / radiation effects
  • Chromosomes, Human, Pair 4 / radiation effects
  • DNA Probes*
  • Dose-Response Relationship, Radiation
  • Humans
  • In Situ Hybridization, Fluorescence
  • In Vitro Techniques
  • Lymphocytes / ultrastructure
  • Male
  • Middle Aged
  • Translocation, Genetic

Substances

  • Cesium Radioisotopes
  • DNA Probes