I. Szumiel1, M. Walicka1, I. Buraczewska1, J. Z. Beer2
1 Department of Radiobiology and Health Protection, Institute of Nuclear Chemistry and Technology, Dorodna 16, 03-195 Warsaw, Poland,
2 Center for Devices and Radiological, Health, Food and Drug Administration,
HFZ-114, Rockville, MD 20857 USA
Chromatin response to ultraviolet-C (254 nm, UVC) radiation was examined in two strains of mouse lymphoma
cells, L5178Y-R (LY-R) and L517SY-S (LY-S), with different UVC sensitivities and post-UVC-exposure repair
capacities. UVC sensitive (X-ray resistant) LY-R cells are impaired in DNA excision and post-replication
repair as compared to the UVC resistant (X-ray sensitive) LY-S cells. Following UVC exposure, the
UVA-assisted photobinding of 8-Methoxypsoralen (8-MOP) to DNA was reduced in LY-S cells (to approximately
60% of the control at 15 min post-exposure), while it was increased in LY-R cells (by approximately 20% at
45 min post-exposure). The nucleoids isolated from irradiated LY-R cells sedimented at a reduced rate,
and this effect persisted for 24 h post-exposure. The nucleoids from irradiated LY-S cells sedimented at
a control rate or faster, except 30 min after exposure (the time of high incision rate), when they
sedimented at a reduced rate. The data indicate qualitative differences in UVC response of LY-R and LY-S
cells at the chromatin level that may be related to different processing of DNA damage by the two cell
strains and may result in modifying the 8-MOP access to DNA.