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来自微核的染色体的跨代追踪

Transgenerational Tracking of Chromosomes from Micronuclei.

作者信息

Tsai Tsung-Lin, Lambuta Ruxandra A, Papathanasiou Stamatis

机构信息

Institute of Molecular Biology, Mainz, Germany.

出版信息

Methods Mol Biol. 2025;2968:385-400. doi: 10.1007/978-1-0716-4750-9_23.

Abstract

A hallmark consequence of errors in mitosis is the generation of aberrant nuclear structures, such as micronuclei and chromosome bridges, which have long been associated with disease like cancer. Groundbreaking recent work showed that whole chromosomes or chromosome segments that transit through such structures can accumulate severe rearrangements and thus contribute to the evolution of complex genetic structural events, collectively called "chromoanagenesis". Despite strong interest in the field of genomic instability, a detailed mechanistic understanding of the choreography of transgenerational events that lead to chromoanagenesis is lacking. This is partly due to limited methodologies currently available for temporally-resolved analysis of the genetic and chromatin properties of chromoanagenesis-generating nuclear structures. Here, we review two novel imaging-based cellular systems that we presented recently, which allow transgenerational tracking of micronucleated chromosomes. Together, we include detailed methodologies for the analysis of their functional properties, specifically transcription and chromatin state. Linking the functional analysis of abnormal chromosomes from micronuclei with their prior history of cellular events offers an invaluable and novel approach towards the dissection of the origins and consequences of chromoanagenesis.

摘要

有丝分裂错误的一个标志性后果是产生异常的核结构,如微核和染色体桥,长期以来它们一直与癌症等疾病相关。最近的开创性研究表明,通过这些结构的整条染色体或染色体片段会积累严重的重排,从而推动复杂遗传结构事件的演变,这些事件统称为“染色体混乱”。尽管基因组不稳定性领域备受关注,但对于导致染色体混乱的跨代事件的详细机制仍缺乏了解。部分原因是目前用于对产生染色体混乱的核结构的遗传和染色质特性进行时间分辨分析的方法有限。在此,我们回顾我们最近提出的两种基于成像的新型细胞系统,它们可以对微核化染色体进行跨代追踪。我们还共同提供了详细的方法来分析它们的功能特性,特别是转录和染色质状态。将微核中异常染色体的功能分析与其先前的细胞事件历史联系起来,为剖析染色体混乱的起源和后果提供了一种宝贵的新方法。

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