Masumura Ken-ichi, Kuniya Kensuke, Kurobe Toshihiro, Fukuoka Masamichi, Yatagai Fumio, Nohmi Takehiko
Division of Genetics and Mutagenesis, National Institute of Health Sciences, Tokyo, Japan.
Environ Mol Mutagen. 2002;40(3):207-15. doi: 10.1002/em.10108.
Heavy-ion radiation accounts for the major component of absorbed cosmic radiation and is thus regarded as a significant risk during long-term manned space missions. To evaluate the genetic damage induced by heavy particle radiation, gpt delta transgenic mice were exposed to carbon particle irradiation and the induced mutations were compared with those induced by reference radiations, i.e., X-rays and gamma-rays. In the transgenic mouse model, deletions and point mutations were individually identified as Spi(-) and gpt mutations, respectively. Two days after 10 Gy of whole-body irradiation, the mutant frequencies (MFs) of Spi(-) and gpt were determined. Carbon particle irradiation significantly increased Spi(-) MF in the liver, spleen, and kidney but not in the testis, suggesting an organ-specific induction of mutations by heavy-ion irradiation. In the liver, the potency of inducing Spi(-) mutation was highest for carbon particles (3.3-fold increase) followed by X-rays (2.1-fold increase) and gamma-rays (1.3-fold increase), while the potency of inducing gpt mutations was highest for gamma-rays (3.3-fold increase) followed by X-rays (2.1-fold increase) and carbon particles (1.6-fold increase). DNA sequence analysis revealed that carbon particles induced deletions that were mainly more than 1,000 base pairs in size, whereas gamma-rays induced deletions of less than 100 base pairs and base substitutions. X-rays induced various-sized deletions and base substitutions. These results suggest that heavy-ion beam irradiation is effective at inducing deletions via DNA double-strand breaks but less effective than X-ray and gamma-ray irradiation at producing oxidative DNA damage by free radicals.
重离子辐射是宇宙辐射吸收的主要组成部分,因此被视为长期载人航天任务中的重大风险。为了评估重粒子辐射引起的遗传损伤,将gpt delta转基因小鼠暴露于碳粒子辐射下,并将诱导的突变与参考辐射(即X射线和γ射线)诱导的突变进行比较。在转基因小鼠模型中,缺失和点突变分别被鉴定为Spi(-)和gpt突变。全身照射10 Gy后两天,测定Spi(-)和gpt的突变频率(MFs)。碳粒子辐射显著增加了肝脏、脾脏和肾脏中的Spi(-) MF,但在睾丸中没有增加,这表明重离子辐射对突变的诱导具有器官特异性。在肝脏中,诱导Spi(-)突变的能力以碳粒子最高(增加3.3倍),其次是X射线(增加2.1倍)和γ射线(增加1.3倍),而诱导gpt突变的能力以γ射线最高(增加3.3倍),其次是X射线(增加2.1倍)和碳粒子(增加1.6倍)。DNA序列分析表明,碳粒子诱导的缺失主要大于1000个碱基对,而γ射线诱导的缺失小于100个碱基对以及碱基替换。X射线诱导各种大小的缺失和碱基替换。这些结果表明,重离子束辐射通过DNA双链断裂有效诱导缺失,但在通过自由基产生氧化性DNA损伤方面不如X射线和γ射线辐射有效。