DNA-repair-deficient Rad54/Rad54B mice are more sensitive to clastogens than wild-type mice

Toxicol Lett. 2008 Dec 15;183(1-3):112-7. doi: 10.1016/j.toxlet.2008.10.005. Epub 2008 Oct 21.

Abstract

The sensitivity of DNA-repair-deficient Rad54/Rad54B mice for clastogens was studied and compared to that of wild-type mice. LacZ mutant frequencies (MF) in Rad54/Rad54B mice, after treatment with mitomycin C (MMC), bleomycin (BLM) and gamma-irradiation, were compared to those of the wild-type mice following the same treatments. While none of the clastogens showed an induction of the lacZ MF in the wild-type mice, there was a significant increase of the lacZ MF in the bone marrow of the Rad54/Rad54B mice after treatment with BLM and gamma-irradiation and in the spleen after MMC treatment. As expected, the positive control ENU showed a significant increase in the lacZ MF in all tested organs in wild-type mice. Mutant colonies were hybridized with total mouse DNA in order to discriminate between small gene mutations and large DNA rearrangements and translocations (size-change mutations). The hybridization studies showed a significant increase in mouse DNA positive clones 4 days after treatment with MMC and BLM in the bone marrow of the wild-type mice, which is indicative for chromosomal rearrangements and translocations to occur. An even more pronounced increase was seen 28 days after treatment with the same compounds in the Rad54/Rad54B mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bleomycin / toxicity
  • Bone Marrow Cells / drug effects
  • Bone Marrow Cells / metabolism
  • Bone Marrow Cells / radiation effects
  • DNA Helicases
  • DNA Repair / genetics*
  • Ethylnitrosourea / toxicity
  • Female
  • Gamma Rays
  • Genotype
  • Lac Operon / genetics
  • Male
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Micronucleus Tests / methods
  • Mitomycin / toxicity
  • Mutagenesis / drug effects
  • Mutagenesis / radiation effects
  • Mutagenicity Tests / methods
  • Mutagens / toxicity*
  • Nuclear Proteins / deficiency
  • Nuclear Proteins / genetics*

Substances

  • Mutagens
  • Nuclear Proteins
  • Bleomycin
  • Mitomycin
  • DNA Helicases
  • Rad54l protein, mouse
  • Ethylnitrosourea