Vorobtsova I E
Radiats Biol Radioecol. 2006 Jul-Aug;46(4):441-6.
Stability of genome is one of the evolutionary important trait of cells. Various mutations (gene, chromosomal, genomic) as well as artificial manipulations with genomes (inbreeding, DNA transfection, introduction of Br-DU in DNA) cause the genetic instability. Ionizing radiation is known as the factor which induced instability of genome in late mitotic descendants of cells after in vitro and in vivo exposure. Radiation induced genetic instability can be transmitted through germline cells. On the cell level both types of radiation induced genomic instability are manifested in elevated frequency of mutations, chromosome aberrations, micronuclei, increased radiosensitivity, disappearance of adaptive response, changes in gene expression. In studies of 1970-1980 years clear evidences on the different morphological and functional injuries in tissues of irradiated organisms as well as in tissues of the progeny of exposed parents were obtained. On the organism level the instability of mitotic and of meiotic progeny of irradiated cells is resulted in increased risk of cancer and of other somatic diseases. It seems to be useful to review the earlier radiobiology literature where delayed and transgenerational effects of ionizing radiation on tissues and on organisms level were clearly shown in animals. For the estimation of pathogenic role of radiation induced genomic instability in humans, particularly in children of exposed parents the parallel study of the same human cohorts using clinical parameters and various characteristic of genomic instability seems to be very important.
基因组稳定性是细胞进化中的一个重要特征。各种突变(基因、染色体、基因组)以及对基因组的人工操作(近亲繁殖、DNA转染、在DNA中引入溴脱氧尿苷)都会导致遗传不稳定。电离辐射是已知的在体外和体内暴露后诱导细胞晚期有丝分裂后代基因组不稳定的因素。辐射诱导的遗传不稳定可通过生殖细胞传递。在细胞水平上,两种类型的辐射诱导的基因组不稳定都表现为突变频率升高、染色体畸变、微核、放射敏感性增加、适应性反应消失以及基因表达变化。在20世纪70 - 80年代的研究中,获得了关于受辐照生物体组织以及受辐照亲代后代组织中不同形态和功能损伤的明确证据。在生物体水平上,受辐照细胞有丝分裂和减数分裂后代的不稳定导致患癌症和其他体细胞疾病的风险增加。回顾早期放射生物学文献似乎是有用的,其中电离辐射对动物组织和生物体水平的延迟和跨代效应在文献中有明确显示。为了评估辐射诱导的基因组不稳定在人类,特别是在受辐照亲代的子女中的致病作用,使用临床参数和基因组不稳定的各种特征对相同人类队列进行平行研究似乎非常重要。