Schwartz J L, Hsie A W
Department of Radiation Oncology, University of Washington, Seattle 98195, USA.
Radiat Res. 1997 Nov;148(5 Suppl):S87-92.
It has been suggested that the more closely spaced, clustered DNA breaks seen with high-LET radiations are more likely to result in chromosome intrachanges than in chromosome interchanges. We determined whether analysis of the spectra of chromosome aberrations or Hprt gene mutations in CHO-K1 cells could detect a shift to more chromosome intrachanges and therefore distinguish exposure to high-LET radiation from exposure to low-LET radiation, and whether alterations in the processing of DNA breaks would influence this process. Both the frequency and type of chromosome aberrations and Hprt gene mutations were determined in CHO-K1 and xrs-5 cells exposed to 60Co gamma rays or 212Bi alpha particles. Xrs-5 cells are a radiosensitive derivative of CHO-K1 cells that are defective in rejoining of DNA double-strand breaks. The ratio of dicentrics to centric rings (F ratio) was significantly lower in CHO-K1 and xrs-5 cells exposed to alpha particles, consistent with a shift to more chromosome intrachanges with higher LET. In contrast, the frequency of large interstitial deletions at the Hprt locus, determined by multiplex polymerase chain reaction-based exon deletion analysis, was the same for both gamma-ray- and alpha-particle-exposed cells in each of the cell lines. Thus the F ratio can distinguish high-LET from low-LET radiations, and the end point is not influenced by differences in the processing of DNA double-strand breaks. The analysis of the spectrum of Hprt mutations, however, appears unable to discriminate low LET from high LET.
有人提出,高传能线密度辐射导致的DNA断裂间距更近、更为聚集,相比染色体间互换,更有可能导致染色体内互换。我们确定,分析中国仓鼠卵巢细胞(CHO-K1)中的染色体畸变谱或次黄嘌呤-鸟嘌呤磷酸核糖转移酶(Hprt)基因突变,是否能检测到向更多染色体内互换的转变,从而区分高传能线密度辐射暴露和低传能线密度辐射暴露,以及DNA断裂处理过程中的改变是否会影响这一过程。在暴露于60Coγ射线或212Biα粒子的CHO-K1和xrs-5细胞中,测定了染色体畸变和Hprt基因突变的频率及类型。Xrs-5细胞是CHO-K1细胞的放射敏感衍生物,在DNA双链断裂重连方面存在缺陷。暴露于α粒子的CHO-K1和xrs-5细胞中,双着丝粒与着丝粒环的比率(F比率)显著更低,这与随着传能线密度升高向更多染色体内互换的转变一致。相比之下,通过基于多重聚合酶链反应的外显子缺失分析测定的,各细胞系中γ射线和α粒子暴露细胞的Hprt基因座处大的中间缺失频率相同。因此,F比率可以区分高传能线密度辐射和低传能线密度辐射,并且该终点不受DNA双链断裂处理差异的影响。然而,Hprt基因突变谱分析似乎无法区分低传能线密度辐射和高传能线密度辐射。