Abstract

DNA single-strand-breakage efficiency was measured in frozen Chinese hamster cells (V79-S171) after they accumulated disintegrations from incorporated tritium. The results are compared to the single-strand-breakage efficiency of X-rays at dry ice or liquid nitrogen temperatures, which is reduced by a factor of 4 from the strand-breakage efficiency found at 37°C.3 H decays in cells that incorporated [5-3 H]uridine into RNA after a 30-min pulse were 20% as effective as those in [3 H]thymidine-labeled cells in causing single-strand breaks in DNA. This difference in DNA strand-breakage efficiencies for [3 H]uridine and [3 H]thymidine is almost the same as the difference in efficiencies of cell killing from the two macromolecular locations of tritium within the nucleus of the cell. In cells labeled in one or both strands of DNA with [3 H]thymidine the breakage efficiencies were 2.2-2.3 breaks per3 H decay, equivalent to 0.5 rads per decay-a value very close to that predicted for the dosimetry of3 H beta partic...

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.