Abstract

Cultures of blood from healthy adults were irradiated 48 h after stimulation with 240 R of X-rays and fixed after various time intervals (0–2 h, 2–4 h, 4–6 h). 3HTdR was added to several cultures after irradiation. Mitotic and labelling indices were used to distinguish between two cell samples inside the irradiated G 2 population: D − cells reaching mitosis without mitotic delay and a high frequency of chromatic breaks and D + cells with mitotic delay and which, during the delay, repair most of the damage produced. After R banding 450 chromatid deletions were located in each of the two cell samples. The D + cells showed a higher frequency of breaks than the D − cells with decreasing chromosome size, in the telomeric and centromeric region and in the junction between the R + and R − bands. These results can be interpreted as indicative of a non-random distribution of repair processes both between and within chromosomes.

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