Delayed DNA damage and radiation-induced genomic instability

Keiji Suzuki, S. Kodama, M. Watanabe
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Abstract

Ionizing radiation induces genomic instability, which is transmitted through many generations after irradi-ation in the progeny of surviving cells. We have hypothesized that radiation-induced large deletion causes potentially unstable chromosome regions, which are involved in delayed induction of radiation-induced genomic instability. Using phosphorylation-specific antibodies against ATM and histone H2AX, whose phos-phorylation is induced by DNA double strand breaks, we detected delayed induction of phosphorylated ATM and H2AX foci in the progeny of X-ray-surviving cells, which indicated delayed induction of DNA double strand breaks. Furthermore, we found delayed chromosomal instability in X chromosomes in clones which contain large deletion involving the HPRT loci. It is suggested that large deletion involving 〜 Mb region causes unstable chromatin structure, and it results in delayed rearrangement of chromosomes involved. These findings provide the possibility that manifestation of radiation-induced genomic instability results from delayed DNA breaks, i.e., the breaks lead to delayed chromosome rearrangements, delayed cell death etc., many generations after irradiation.
延迟DNA损伤和辐射诱导的基因组不稳定性
电离辐射诱导基因组不稳定,这种不稳定在辐照后存活细胞的后代中通过许多代传递。我们假设辐射诱导的大缺失会导致潜在的不稳定染色体区域,这与辐射诱导的基因组不稳定的延迟诱导有关。利用针对ATM和组蛋白H2AX(其磷酸化可由DNA双链断裂诱导)的磷酸化特异性抗体,我们在x射线存活细胞的后代中检测到延迟诱导磷酸化的ATM和H2AX灶,这表明延迟诱导DNA双链断裂。此外,我们发现在含有大量HPRT位点缺失的克隆中,X染色体的延迟染色体不稳定性。提示~ Mb区的大缺失导致染色质结构不稳定,导致相关染色体的重排延迟。这些发现提供了一种可能性,即辐射引起的基因组不稳定的表现是由于DNA断裂的延迟,即断裂导致染色体重排的延迟,细胞死亡的延迟等,在辐射后许多代。
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