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Amplification of oncogenes and integrated SV40 sequences in mammalian cells by the decay of incorporated iodine-125

Journal Article · · Radiat. Res.; (United States)
DOI:https://doi.org/10.2307/3576968· OSTI ID:6846798
Iodine-125, in the form of 5-(/sup 125/I)iododeoxyuridine (I-UdR), was incorporated into the DNA of SV40 transformed Chinese hamster embryo cells. Disintegration of the /sup 125/I led to increased cell killing with increasing dose as measured by the colony-forming ability of single cells. The D37 (the dose at which 37% of the cells survive) amounts to 95 decays per cell, corresponding to 0.66 Gy. Variations in the copy number of specific DNA sequences was measured by using dispersed cell blotting with sensitive DNA hybridizations. A 13-fold amplification of the viral DNA sequences (SV40) and a twofold amplification of two cellular oncogenes of the ras-family (Ki-ras and Ha-ras) were found. Other cellular genes, like the alpha-actin gene, were not amplified, and no variation in gene copy number was detected after incubation of cells with cold I-UdR. We suggest the observed gene amplifications are induced by the densely ionizing radiation emitted by the decay of the incorporated /sup 125/I atoms.
Research Organization:
Institut fuer Genetik und fuer Toxikologie von Spaltstoffen, Germany, F.R.
OSTI ID:
6846798
Journal Information:
Radiat. Res.; (United States), Journal Name: Radiat. Res.; (United States) Vol. 1; ISSN RAREA
Country of Publication:
United States
Language:
English

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