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灾难性事件后染色体的重建:染色体重排的新兴机制。

Rebuilding Chromosomes After Catastrophe: Emerging Mechanisms of Chromothripsis.

机构信息

Ludwig Institute for Cancer Research, Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA 92093, USA.

出版信息

Trends Cell Biol. 2017 Dec;27(12):917-930. doi: 10.1016/j.tcb.2017.08.005. Epub 2017 Sep 9.

Abstract

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.

摘要

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。

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