Abstract
Exposure of mammalian cells to a variety of chemical and physical agents depresses the overal rate of DNA synthesis [1]. Part of this inhibition can be ascribed to a disturbance of the initiation of cell DNA replication. The cellular genome comprises numerous units which contain each one replication origin and are replicated sequentially. Genotoxic agents, in particular direct or indirect inducers of DNA breaks, apparently delay the initiation of the replication of units normally programmed for a time subsequent to the treatment of the cells [2]. Single-strand breaks might lead to the loss of chromosomal segments if not sealed at the time of replication. The temporary inhibition of the initiation of DNA replication lowers this risk by providing cells with more time for DNA repair. The lack of a delay in DNA replication displayed by human cells derived from Ataxia telangiectasia patients is associated with an increased sensitivity to the lethal effect of the treatment [3].
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Rommelaere, J., Vos, JM., Ward, D.C. (1983). Parvoviral Probe of DNA Replication in Mammalian Cells Exposed to Genotoxic Agents. In: Castellani, A. (eds) The Use of Human Cells for the Evaluation of Risk from Physical and Chemical Agents. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-1117-2_18
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DOI: https://doi.org/10.1007/978-1-4757-1117-2_18
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