Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Cell. 2011 Sep 16;146(6):889-903. doi: 10.1016/j.cell.2011.07.042.
Complex genomic rearrangements (CGRs) consisting of two or more breakpoint junctions have been observed in genomic disorders. Recently, a chromosome catastrophe phenomenon termed chromothripsis, in which numerous genomic rearrangements are apparently acquired in one single catastrophic event, was described in multiple cancers. Here, we show that constitutionally acquired CGRs share similarities with cancer chromothripsis. In the 17 CGR cases investigated, we observed localization and multiple copy number changes including deletions, duplications, and/or triplications, as well as extensive translocations and inversions. Genomic rearrangements involved varied in size and complexities; in one case, array comparative genomic hybridization revealed 18 copy number changes. Breakpoint sequencing identified characteristic features, including small templated insertions at breakpoints and microhomology at breakpoint junctions, which have been attributed to replicative processes. The resemblance between CGR and chromothripsis suggests similar mechanistic underpinnings. Such chromosome catastrophic events appear to reflect basic DNA metabolism operative throughout an organism's life cycle.
复杂基因组重排(CGR)由两个或多个断点连接组成,已在基因组疾病中观察到。最近,在多种癌症中描述了一种称为染色体重排的染色体灾难现象,其中许多基因组重排显然是在一次单一的灾难性事件中获得的。在这里,我们表明,获得性 CGR 与癌症染色体重排具有相似性。在研究的 17 个 CGR 病例中,我们观察到了局部和多个拷贝数变化,包括缺失、重复和/或三倍体,以及广泛的易位和倒位。基因组重排的大小和复杂性各不相同;在一个病例中,阵列比较基因组杂交显示了 18 个拷贝数变化。断裂点测序确定了特征性特征,包括断裂点处的小模板插入和断裂点连接处的微同源性,这些特征归因于复制过程。CGR 和染色体重排之间的相似性表明存在类似的机制基础。这种染色体灾难性事件似乎反映了整个生物体生命周期中基本的 DNA 代谢。