Limoli C L, Kaplan M I, Corcoran J, Meyers M, Boothman D A, Morgan W F
Department of Radiation Oncology, University of California, San Francisco 94143-0750, USA.
Cancer Res. 1997 Dec 15;57(24):5557-63.
Chromosomal destabilization is one end point of the more general phenomenon of genomic instability. We previously established that chromosomal instability can manifest in clones derived from single progenitor cells several generations after X-irradiation. To understand the potential relationship between chromosomal destabilization and the other end points of genomic instability, we generated a series of chromosomally stable and unstable clones by exposure to X-rays. All clones were derived from the human-hamster hybrid line GM10115, which contains a single copy of human chromosome 4 in a background of 20-24 hamster chromosomes. These clones were then subjected to a series of assays to determine whether chromosomal instability is associated with a general "mutator phenotype" and whether it modulates other end points of genomic instability. Thus, we analyzed clones for sister chromatid exchange, delayed reproductive cell death, delayed mutation, mismatch repair, and delayed gene amplification. Statistical analyses performed on each group of chromosomally stable and unstable clones indicated that, although individual clones within each group were significantly different from unirradiated clones for many of the end points, there was no significant correlation between chromosomal instability and sister chromatid exchange, delayed mutation, and mismatch repair. Delayed gene amplification was found to be marginally correlated to chromosomal instability (P < 0.1), and delayed reproductive cell death (the persistent reduction in plating efficiency after irradiation) was found to be significantly correlated (P < 0.05). These correlations may be explained by chromosomal destabilization, which can mediate gene amplification and can result in cellular lethality. These data implicate multiple molecular and genetic pathways leading to different manifestations of genomic instability in GM10115 cells surviving exposure to DNA-damaging agents.
染色体不稳定是基因组不稳定这一更为普遍现象的一个终点。我们之前证实,染色体不稳定可在X射线照射后几代由单个祖细胞衍生而来的克隆中表现出来。为了理解染色体不稳定与基因组不稳定的其他终点之间的潜在关系,我们通过暴露于X射线产生了一系列染色体稳定和不稳定的克隆。所有克隆均源自人-仓鼠杂交细胞系GM10115,该细胞系在20 - 24条仓鼠染色体的背景下含有单拷贝的人类4号染色体。然后对这些克隆进行一系列检测,以确定染色体不稳定是否与一般的“突变体表型”相关,以及它是否调节基因组不稳定的其他终点。因此,我们分析了克隆的姐妹染色单体交换、延迟生殖细胞死亡、延迟突变、错配修复和延迟基因扩增情况。对每组染色体稳定和不稳定克隆进行的统计分析表明,尽管每组中的单个克隆在许多终点方面与未照射的克隆有显著差异,但染色体不稳定与姐妹染色单体交换、延迟突变和错配修复之间没有显著相关性。发现延迟基因扩增与染色体不稳定存在微弱相关性(P < 0.1),并且发现延迟生殖细胞死亡(照射后接种效率的持续降低)存在显著相关性(P < 0.05)。这些相关性可能由染色体不稳定来解释,染色体不稳定可介导基因扩增并可导致细胞致死。这些数据表明,在暴露于DNA损伤剂后存活的GM10115细胞中,多种分子和遗传途径导致了基因组不稳定的不同表现形式。