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Cell lethality after selective irradiation of the DNA replication fork

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Summary

It has been suggested that nascent DNA located at the DNA replication fork may exhibit enhanced sensitivity to radiation damage. To evaluate this hypothesis, Chinese hamster ovary cells (CHO) were labeled with125I-iododeoxyuridine (125IUdR) either in the presence or absence of aphidicolin. Aphidicolin (5 µg/ml) reduced cellular125IUdR incorporation to 3–5% of the control value. The residual125I incorporation appeared to be restricted to low molecular weight (sub-replicon sized) fragments of DNA which were more sensitive to micrococcal nuclease attack and less sensitive to high salt DNase I digestion than randomly labeled DNA. These findings suggest that DNA replicated in the presence of aphidicolin remains localized at the replication fork adjacent to the nuclear matrix.

Based on these observations an attempt was made to compare the lethal consequences of125I decays at the replication fork to that of125I decays randomly distributed over the entire genome. Regardless of the distribution of decay events, all treatment groups exhibited identical dose-response curves (D0: 101125I decays/cell). Since differential irradiation of the replication complex did not result in enhanced cell lethality, it can be concluded that neither the nascent DNA nor the protein components (replicative enzymes, nuclear protein matrix) associated with the DNA replication site constitute key radiosensitive targets within the cellular genome.

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Authors and Affiliations

  1. Institute of Molecular Biophysics Florida State University Tallahassee, 32306, FL, USA

    K. G. Hofer

  2. Radiology Department University of Utah Medical Center Salt Lake City, 84132, UT, USA

    R. L. Warters

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  1. K. G. Hofer
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  2. R. L. Warters
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Hofer, K.G., Warters, R.L. Cell lethality after selective irradiation of the DNA replication fork. Radiat Environ Biophys 24, 161–174 (1985). https://doi.org/10.1007/BF01209520

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  • DOI: https://doi.org/10.1007/BF01209520

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