Abstract

The kinetics of x-ray-induced single-strand break rejoinirg have been studied in wild-type M. radiodurans and a radiosensitive mutant, UV17. The initial fast rejoining reaction observed in wild-type cells in growth medium was absent in UV17. Studies in which irradiated cells were allowed to repair under various conditions confirm that a buffer-mediated rejoining system is absent in UV17 while rejoining of strand breaks under growth conditions is slower but not absent DNA breakdown is more extensive in UV17 although its rate is similar to that of the wild-type. In both strains the x-ray-induced DNA synthesis delay and the time for maximal release of acid-soluble material correlate. In vitro studies show the capacity of lysates of wild-type and mutant cells to catalyze the incorporation of deoxyribonucleotide triphosphates into acid-insoluble material are similar while DNase activity in the mutant is much greater than in the wild type. The in vitro data are correlated with the in vivo observations and indicate that the sensitivity of UV17 to ionizing radiation may be the result of an inhibition of DNA polymerase-mediated repair and not a consequence of an exr or lex type of mutation as has been previously thought.

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.