首页> 外文期刊>Radiation Research: Official Organ of the Radiation Research Society >The effect of dose rate on the frequency of specific-locus mutations induced in mouse spermatogonia is restricted to larger lesions; A retrospective analysis of historical data
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The effect of dose rate on the frequency of specific-locus mutations induced in mouse spermatogonia is restricted to larger lesions; A retrospective analysis of historical data

机译:剂量率对小鼠精原细胞中特异性基因座突变频率的影响仅限于较大的病变。历史数据的回顾性分析

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摘要

A series of 19 large-scale germ-cell mutagenesis experiments conducted several decades ago led to the conclusion that low-LET radiation delivered to mouse spermatogonia at dose rates of 0.8 R/min and below induced only about one-third as many specific-locus mutations as did single, acute exposures at 24 R/min and above. A two-hit origin of the mutations was deemed unlikely in view of the then prevailing evidence for the small size of genetic lesions in spermatogonia. Instead, the dose-rate effect was hypothesized to be the result of a repair system that exists in spermatogonia, but not in more mature male reproductive cells. More recent genetic and molecular studies on the marker genes have identified the phenotypes associated with specific states of the mutant chromosomes, and it is now possible retrospectively to classify individual past mutations as "large lesions" or "other lesions". The mutation-frequency difference between high and low dose rates is restricted to the large lesion mutations, for which the dose-curve slopes differ by a factor exceeding 3.4. For other lesion mutations, there is essentially no difference between the slopes for protracted and acute irradiations; induced other lesions frequencies per unit dose remain similar for dose rates ranging over more than 7 orders of magnitude. For large lesions, these values rise sharply at dose rates >0.8 R/min, though they remain similar within the whole range of protracted doses, failing to provide evidence for a threshold dose rate. The downward bend at high doses that had been noted for X-ray-induced specific-locus mutations as a whole and ascribed to a positive correlation between spermatogonial death and mutation load is now found to be restricted to large lesion mutations. There is a marked difference between the mutation spectra (distributions among the seven loci) for large lesions and other lesions. Within each class, however, the spectra are similar for acute and protracted irradiation.
机译:几十年前进行的一系列19项大规模生殖细胞诱变实验得出的结论是,低LET辐射以0.8 R / min及以下的剂量率传递至小鼠精原细胞仅诱导约三分之一的特异性位点与24 R / min及以上的单次,急性暴露一样发生突变。鉴于当时普遍存在的精原细胞遗传病灶较小的证据,认为突变不会两次被击中。取而代之的是,剂量率效应被认为是精子细胞中存在修复系统的结果,而在成熟的雄性生殖细胞中则没有。关于标记基因的最新的遗传和分子研究已经鉴定了与突变体染色体的特定状态相关的表型,并且现在有可能回顾性地将过去的单个突变分类为“大损伤”或“其他损伤”。高剂量率和低剂量率之间的突变频率差异仅限于较大的病变突变,对于这些突变,剂量曲线的斜率相差超过3.4。对于其他病变突变,长期照射和急性照射的斜率之间基本上没有差异;对于超过7个数量级的剂量率,每单位剂量引起的其他病变频率仍然相似。对于较大的病灶,这些值在剂量率> 0.8 R / min时会急剧上升,尽管在整个长期剂量范围内仍保持相似,但无法提供阈值剂量率的证据。总体上,X射线诱导的特定基因座突变已注意到高剂量的向下弯曲,归因于精原细胞死亡和突变负荷之间的正相关性,现在发现这种弯曲仅限于大病变突变。大病变和其他病变的突变谱(七个基因座之间的分布)之间存在显着差异。但是,在每个类别中,急性和长时间照射的光谱相似。

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