Doherty Ann T, Baumgartner Adi, Anderson Diana
Safety Assessment, AstraZeneca, Cheshire, UK.
Methods Mol Biol. 2012;817:271-304. doi: 10.1007/978-1-61779-421-6_14.
Chromosome aberration assays are employed to detect the induction of chromosome breakage (clastogenesis) in somatic and germ cells by direct observation of the chromosomal damage during metaphase analysis, or by indirect observation of chromosomal fragments. Thus, various types of cytogenetic change can be detected such as structural chromosome aberrations (CA), sister chromatid exchanges (SCE), ploidy changes, and micronuclei. Following the induction of the chromosomal damage, most of the aberrations and abnormalities detected by these assays can be detrimental or even lethal to the cell. Their presence, however, indicates a potential to also induce more subtle and therefore transmissible chromosomal damage which survives cell division to produce heritable cytogenetic changes. Usually, induced cytogenetic damage is accompanied by other genotoxic damage such as gene mutations.
染色体畸变分析用于通过在中期分析期间直接观察染色体损伤,或间接观察染色体片段,来检测体细胞和生殖细胞中染色体断裂(断裂发生)的诱导情况。因此,可以检测到各种类型的细胞遗传学变化,如染色体结构畸变(CA)、姐妹染色单体交换(SCE)、倍性变化和微核。在诱导染色体损伤后,这些分析检测到的大多数畸变和异常对细胞可能是有害的甚至是致命的。然而,它们的存在表明也有可能诱导更细微且因此可遗传的染色体损伤,这种损伤在细胞分裂后存活下来,产生可遗传的细胞遗传学变化。通常,诱导的细胞遗传学损伤伴随着其他遗传毒性损伤,如基因突变。