Sachs R K, Brenner D J, Hahnfeldt P J, Hlatkys L R
Department of Mathematics, University of California, Berkeley 94720, USA.
Int J Radiat Biol. 1998 Aug;74(2):185-206. doi: 10.1080/095530098141573.
To model intrachromosomal clustering of DSB (DNA double strand breaks) induced by ionizing radiation. That DSB are located non-randomly along chromosomes after high LET irradiation, with clustering even at extremely large scales, has been confirmed by recent pulsed field gel electrophoresis data for size distributions of DNA fragments. We therefore extend the standard random-breakage model for DNA fragment-size distributions to a more general 'clustered-breakage' formalism, which can take correlations of DSB locations along a chromosome into account.
The new formalism is based mainly on a one-track probability distribution, describing the DNA fragment-size pattern due to a single primary high-energy particle, a pattern determined by track structure and chromatin geometry. Multi-track fragment-size distributions are derived mathematically from the one-track distribution, so that dose response relations are obtained.
The clustered-breakage formalism is applicable to any chromosomal geometry and any radiation track structure. It facilitates extrapolations of high-dose data to the much lower doses of interest for most applications. When applied to recently published data for irradiation of mammalian cells with ions of LET approximately 100 keV microm(-1) it indicates a pattern of Mbp-scale DSB clusters, each containing a number of DSB and corresponding to a very large-scale, multiply-damaged chromatin site. Although DSB are bunched, DSB clusters are scattered almost at random throughout the genome. Estimates of DSB yield are markedly increased by resolving such clusters into individual DSB. The dose response relation for fragments of a given size becomes non-linear when clusters from different tracks interlace or adjoin, as can occur for high doses and large sizes.
DSB clustering along chromosomes, which influences important radiobiological endpoints, is described quantitatively by the clustered-breakage formalism.
对电离辐射诱导的DNA双链断裂(DSB)的染色体内聚类进行建模。最近关于DNA片段大小分布的脉冲场凝胶电泳数据证实,在高传能线密度(LET)辐射后,DSB沿染色体非随机定位,甚至在极大尺度上也存在聚类现象。因此,我们将用于DNA片段大小分布的标准随机断裂模型扩展为更通用的“聚类断裂”形式体系,该体系可以考虑DSB沿染色体位置的相关性。
新的形式体系主要基于单轨迹概率分布,描述单个初级高能粒子产生的DNA片段大小模式,这种模式由轨迹结构和染色质几何形状决定。多轨迹片段大小分布通过数学方法从单轨迹分布推导得出,从而获得剂量响应关系。
聚类断裂形式体系适用于任何染色体几何形状和任何辐射轨迹结构。它有助于将高剂量数据外推到大多数应用中感兴趣的低得多的剂量。当应用于最近发表的关于用LET约为100 keV·μm⁻¹的离子照射哺乳动物细胞的数据时,它表明存在兆碱基(Mbp)尺度的DSB聚类模式,每个聚类包含多个DSB,对应于一个非常大尺度的、多重受损的染色质位点。尽管DSB成束,但DSB聚类几乎随机散布在整个基因组中。将这些聚类解析为单个DSB会显著提高DSB产额的估计值。当来自不同轨迹的聚类交错或相邻时,给定大小片段的剂量响应关系会变得非线性,高剂量和大尺寸时可能会出现这种情况。
聚类断裂形式体系定量描述了沿染色体的DSB聚类,这会影响重要的放射生物学终点。