Ludwig Institute for Cancer Research, Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA 92093, USA.
Trends Cell Biol. 2017 Dec;27(12):917-930. doi: 10.1016/j.tcb.2017.08.005. Epub 2017 Sep 9.
Cancer genome sequencing has identified chromothripsis, a complex class of structural genomic rearrangements involving the apparent shattering of an individual chromosome into tens to hundreds of fragments. An initial error during mitosis, producing either chromosome mis-segregation into a micronucleus or chromatin bridge interconnecting two daughter cells, can trigger the catastrophic pulverization of the spatially isolated chromosome. The resultant chromosomal fragments are religated in random order by DNA double-strand break repair during the subsequent interphase. Chromothripsis scars the cancer genome with localized DNA rearrangements that frequently generate extensive copy number alterations, oncogenic gene fusion products, and/or tumor suppressor gene inactivation. Here we review emerging mechanisms underlying chromothripsis with a focus on the contribution of cell division errors caused by centromere dysfunction.
癌症基因组测序已经确定了染色体重排,这是一类复杂的结构基因组重排,涉及单个染色体的明显碎裂成数十到数百个片段。在有丝分裂过程中的初始错误,导致染色体错误分离到微核或连接两个子细胞的染色质桥中,可能会引发空间隔离的染色体灾难性粉碎。随后的细胞间期中,通过 DNA 双链断裂修复,将产生的染色体片段以随机顺序重新连接。染色体重排会在癌症基因组上留下局部 DNA 重排的痕迹,这些重排通常会产生广泛的拷贝数改变、致癌基因融合产物和/或肿瘤抑制基因失活。在这里,我们综述了染色体重排的新兴机制,重点关注由着丝粒功能障碍引起的细胞分裂错误的贡献。