Radiation-induced chromosome aberrations analysed by fluorescence in situ hybridization with a triple combination of composite whole chromosome-specific DNA probes

Int J Radiat Biol. 1992 Dec;62(6):673-8. doi: 10.1080/09553009214552621.

Abstract

Fluorescence in situ hybridization (FISH) with a combination of three composite whole chromosome-specific DNA probes for human chromosomes 1, 4 and 12 was used to analyse in vitro radiation-induced dicentrics and symmetrical translocations in peripheral lymphocytes. Translocations could be rapidly and efficiently detected by FISH. Their frequencies were 1.8-fold higher than the frequencies for dicentrics at a given dose. The dose-response curves for translocations and dicentrics were linear quadratic with a significant higher quadratic component for translocations. The application of FISH for scoring stable translocations for biological dosimetry of radiation exposures is discussed.

MeSH terms

  • Adult
  • Blood / radiation effects*
  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 1 / radiation effects*
  • Chromosomes, Human, Pair 12 / radiation effects*
  • Chromosomes, Human, Pair 4 / radiation effects*
  • DNA Probes
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence*
  • In Vitro Techniques
  • Male
  • Middle Aged
  • Radiation Genetics

Substances

  • DNA Probes