Department of Molecular Medicine and Institute of Biotechnology, University of Texas Health Science Center, San Antonio, TX 78245, USA.
Exp Biol Med (Maywood). 2013 Mar;238(3):285-93. doi: 10.1177/1535370213480700.
Many genotoxins are found in the environment from synthetic to natural, yet very few have been studied in depth. This means we fail to understand many molecules that damage DNA, we do not understand the type of damage they cause and the repair pathways required to correct their lesions. It is surprising so little is known about the vast majority of genotoxins since they have potential to cause disease from developmental defects to cancer to degenerative ailments. By contrast, some of these molecules have commercial and medical potential and some can be weaponized. Therefore, we need a systematic method to efficiently generate a genotoxic profile for these agents. A genotoxic profile would include the type of damage the genotoxin causes, the pathways used to repair the damage and the resultant mutations if repair fails. Mouse embryonic stem (ES) cells are well suited for identifying pathways and mutations. Mouse ES cells are genetically tractable and many DNA repair mutant cells are available. ES cells have a high mitotic index and form colonies so experiments can be completed quickly and easily. Furthermore, ES cells have robust DNA repair pathways to minimize genetic mutations at a particularly vulnerable time in life, early development when a mutation in a single cell could ultimately contribute to a large fraction of the individual. After an initial screen, other types of cells and mouse models can be used to complement the analysis. This review discusses the merging field of genotoxic screens in mouse ES cells that can be used to discover and study potential genotoxic activity for chemicals commonly found in our environment.
许多遗传毒素存在于环境中,从合成到天然,然而只有很少一部分被深入研究。这意味着我们无法了解许多损伤 DNA 的分子,我们不了解它们造成的损伤类型以及修复损伤所需的途径。令人惊讶的是,我们对绝大多数遗传毒素知之甚少,因为它们有可能从发育缺陷到癌症到退行性疾病引起疾病。相比之下,这些分子中的一些具有商业和医疗潜力,有些可以被武器化。因此,我们需要一种系统的方法来有效地生成这些试剂的遗传毒性特征。遗传毒性特征将包括遗传毒素引起的损伤类型、修复损伤的途径以及如果修复失败导致的突变。小鼠胚胎干细胞(ES)非常适合识别途径和突变。小鼠 ES 细胞具有遗传可操作性,并且有许多 DNA 修复突变细胞可用。ES 细胞具有较高的有丝分裂指数,并形成集落,因此实验可以快速轻松地完成。此外,ES 细胞具有强大的 DNA 修复途径,以最大限度地减少生命早期发育过程中遗传突变,此时单个细胞中的突变最终可能导致个体的很大一部分发生突变。在初始筛选之后,可以使用其他类型的细胞和小鼠模型来补充分析。这篇综述讨论了在小鼠 ES 细胞中进行遗传毒性筛选的融合领域,该领域可用于发现和研究我们环境中常见化学物质的潜在遗传毒性活性。