Genome Biology Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
Cell. 2013 Mar 14;152(6):1226-36. doi: 10.1016/j.cell.2013.02.023.
Chromothripsis scars the genome when localized chromosome shattering and repair occurs in a one-off catastrophe. Outcomes of this process are detectable as massive DNA rearrangements affecting one or a few chromosomes. Although recent findings suggest a crucial role of chromothripsis in cancer development, the reproducible inference of this process remains challenging, requiring that cataclysmic one-off rearrangements be distinguished from localized lesions that occur progressively. We describe conceptual criteria for the inference of chromothripsis, based on ruling out the alternative hypothesis that stepwise rearrangements occurred. Robust means of inference may facilitate in-depth studies on the impact of, and the mechanisms underlying, chromothripsis.
当局部染色体破碎和修复在一次性灾难中发生时,染色体重排会给基因组留下痕迹。这个过程的结果可以检测到,表现为影响一个或几个染色体的大规模 DNA 重排。尽管最近的研究结果表明染色体重排在癌症发展中起着至关重要的作用,但这个过程的可重复性推断仍然具有挑战性,需要将灾难性的一次性重排与逐步发生的局部损伤区分开来。我们基于排除逐步重排发生的替代假设,描述了推断染色体重排的概念标准。稳健的推断方法可能会促进对染色体重排的影响和机制的深入研究。