Kolb Thorsten, Ernst Aurélie
Group Genome Instability in Tumors, German Cancer Research Centre (DKFZ), Heidelberg, Germany.
Int J Cancer. 2021 May 1. doi: 10.1002/ijc.33618.
Chromothripsis is a form of genomic instability that was shown to play a major role in cancer. Beyond cancer, this type of catastrophic event is also involved in germline structural variation, genome mosaicism in somatic tissues, infertility, mental retardation, congenital malformations and reproductive development in plants. Several assays have been developed to model chromothripsis in vitro and to dissect the mechanistic basis of this phenomenon. Cell-based model systems are designed with different strategies, such as the formation of nuclear structures called micronuclei, telomere fusions or the induction of exogenous DNA double-strand breaks. Here, we review a range of model systems for chromothripsis and the mechanistic insights gained from these assays, with a particular focus on chromothripsis in cancer.
染色体碎裂是基因组不稳定的一种形式,已被证明在癌症中起主要作用。除癌症外,这种灾难性事件还涉及种系结构变异、体细胞组织中的基因组镶嵌现象、不孕、智力迟钝、先天性畸形以及植物的生殖发育。已经开发了几种试验来在体外模拟染色体碎裂并剖析这种现象的机制基础。基于细胞的模型系统采用了不同的策略进行设计,例如形成称为微核的核结构、端粒融合或诱导外源性DNA双链断裂。在这里,我们综述了一系列用于染色体碎裂的模型系统以及从这些试验中获得的机制见解,特别关注癌症中的染色体碎裂。