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18 S rRNA degradation is not accompanied by altered rRNA transport at early times following irradiation of HeLa cells

Journal Article · · Radiation Research; (USA)
DOI:https://doi.org/10.2307/3577565· OSTI ID:7025394
; ; ;  [1]
  1. Israel Institute for Biological Research, Ness-Ziona (Israel)
The effect of ionizing radiation ({sup 137}Cs) on processing and transport of ribosomal RNA (rRNA) was studied by pulse-labeling HeLa S3 cells with ({sup 3}H)uridine immediately prior to irradiation. This approach permits kinetic analysis of processing of 45 S rRNA (radiolabeled predominantly prior to irradiation) into its 28 S and 18 S rRNA daughter species following irradiation. By this technique, we have recently demonstrated an increase in the normal 28 S:18 S rRNA stoichiometric ratio of 1:1 to as high as 1.6:1 during the interval 5 to 20 h following irradiation of HeLa cells at greater than or equal to 7.5 Gy. Alterations in 28 S:18 S ratio were evaluated in greater detail at early times following irradiation, up to 2 h. The 28 S:18 S ratio was found to be maximal at 1 h after radiation, at about 2:1, following 5 or 10 Gy. Using a method for rapid separation of nucleus from cytoplasm, transport of rRNA from nucleus to cytoplasm was also evaluated during this period. Despite an increase in the rate of 45 S rRNA processing, as well as an increased 28 S:18 S ratio, no alterations in transport from nucleus to cytoplasm were detected. This lack of transport alteration suggests that accumulation of excess 28 S rRNA is restricted to the nucleus, where it may represent an early step in the process of radiation-induced cell killing.
OSTI ID:
7025394
Journal Information:
Radiation Research; (USA), Journal Name: Radiation Research; (USA) Vol. 121:1; ISSN 0033-7587; ISSN RAREA
Country of Publication:
United States
Language:
English