Aim:
The chromosomal aberrations induced by radiation appear about nonrandomly
distributed across the whole genome. Previous studies have shown that
chromosomes with high DNA content are less frequently involved in the
formation of symmetrical translocations and dicentric chromosomes than
expected, whereas smaller chromosomes are more frequently involved. We
hypothesized that these translocation regions are linked to radiation
sensitivity.
Materials and methods:
We investigated the frequencies of chromosome translocations induced by
radiation exposure and adjusted the results according to chromosome length.
We specifically analyzed whole blood samples from 3 participants. The
samples were irradiated using
60
Co at doses of 0.5, 1, 2.5, and 5
Gy. Traditional Giemsa-trypsin-Wright band staining was performed to
identify the translocations in the chromosomes, and results were compared
with microarray data generated in our previous study.
Results:
Our analysis indicated that chromosomes 9q were the most sensitive to
translocations after various doses of radiation, and such translocations
occurred in the euchromatin region. Chromosomes 1, 9, 15, and 17 were more
sensitive to radiation doses of 0.5 Gy. This observation could be useful
when selecting sensitive reference chromosomes in the low-dose region. The
results of expression profiling analysis for radiation-sensitive regions
were similar to those of chromosome translocation analysis.
Conclusion:
This study shows that some chromosomes or genomic regions are more sensitive
to alteration by radiation exposure.