Department of Biology, Eastern Michigan University, Ypsilanti, Michigan, USA
Ann N Y Acad Sci. 2012 Sep;1267(1):24-30. doi: 10.1111/j.1749-6632.2012.06592.x.
Certain chromosomal regions called common fragile sites are prone to difficulty during replication. Many tumors have been shown to contain alterations at fragile sites. Several models have been proposed to explain why these sites are unstable. Here we describe work to investigate models of fragile site instability using a yeast artificial chromosome carrying human DNA from a common fragile site region. In addition, we describe a yeast system to investigate whether repair of breaks at a naturally occurring fragile site in yeast, FS2, involves mitotic recombination between homologous chromosomes, leading to loss of heterozygosity (LOH). Our initial evidence is that repair of yeast fragile site breaks does lead to LOH, suggesting that human fragile site breaks may similarly contribute to LOH in cancer. This work is focused on gaining understanding that may enable us to predict and prevent the situations and environments that promote genetic changes that contribute to tumor progression.
某些被称为常见脆弱位点的染色体区域在复制过程中容易出现问题。已经表明许多肿瘤在脆弱位点处存在改变。已经提出了几种模型来解释为什么这些位点不稳定。在这里,我们描述了使用携带来自常见脆弱位点区域的人类 DNA 的酵母人工染色体来研究脆弱位点不稳定性模型的工作。此外,我们还描述了一种酵母系统,用于研究酵母中自然发生的脆弱位点 FS2 的断裂修复是否涉及同源染色体之间的有丝分裂重组,从而导致杂合性丢失 (LOH)。我们的初步证据表明,酵母脆弱位点断裂的修复确实会导致 LOH,这表明人类脆弱位点断裂可能同样导致癌症中的 LOH。这项工作的重点是获得可能使我们能够预测和预防促进导致肿瘤进展的遗传变化的情况和环境的理解。