Mutation studies in lacI transgenic mice after exposure to radiation or cyclophosphamide
Author(s) -
Katharine P. Hoyes,
P. Wadeson,
H.L. Sharma,
J.H. Hendry,
Ian D. Morris
Publication year - 1998
Publication title -
mutagenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.723
H-Index - 91
eISSN - 1464-3804
pISSN - 0267-8357
DOI - 10.1093/mutage/13.6.607
Subject(s) - mutation , spleen , cyclophosphamide , transgene , mutation frequency , lac repressor , genetically modified mouse , microbiology and biotechnology , ionizing radiation , biology , mutagenesis , genetics , irradiation , immunology , gene , lac operon , gene expression , chemotherapy , physics , nuclear physics
We have used the Big Blue lacI transgenic mouse reporter system to investigate mutation induction in the testes, spleen and liver after exposure to an internally incorporated radionuclide, 114mIn, whole body irradiation with 60Co gamma-rays and systemically administered cyclophosphamide. Spontaneous mutation frequencies were 6-17x10(-6). No statistically significant mutation induction was observed in testes or spleen at 35 days after exposure to any test agent, although mutation frequencies tended to be increased (by approximately 1.5-fold) after exposure to 1 Gy gamma-rays. However, liver mutation frequencies were doubled after treatment with 100 mg/kg cyclophosphamide and were elevated by approximately 2.5-fold after systemic administration of 114mIn and 4.5-fold after 1 Gy 60Co gamma-rays. When data from all organs were pooled, mutation frequency was doubled after exposure to 1 Gy gamma-rays, but no other significant increases were observed. These findings support the hypothesis that the lacI transgenic mouse may be relatively inefficient at detecting mutations induced by exposure to ionizing radiation or other agents which produce a spectrum of deletion sizes, including those which are larger than the lacI transgene.
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