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染色体组发生过程中微核的起源与命运

Origin and Fate of Micronuclei on the Road to Chromoanagenesis.

作者信息

Degrassi Francesca, Russo Antonella

机构信息

Institute of Molecular Biology and Pathology, IBPM, National Research Council, CNR, Rome, Italy.

Department of Molecular Medicine, University of Padova, Padova, Italy.

出版信息

Methods Mol Biol. 2025;2968:361-372. doi: 10.1007/978-1-0716-4750-9_21.


DOI:10.1007/978-1-0716-4750-9_21
PMID:40884655
Abstract

Chromoanagenesis defines a group of highly complex chromosome rearrangements restricted to a single or few chromosomes that are suggested to occur in a single catastrophic event. Several experimental findings have connected chromoanagenesis to the formation of micronuclei, small extranuclear chromatin structures harboring a missegregated chromosome or a chromosome fragment. Experimental evidence points to the intrinsic fragility of the envelope around micronuclei as cause of membrane rupture. Consequently, the micronuclear DNA is exposed to various cytoplasmic activities producing the pattern of localized multiple breaks characteristic of chromoanagenesis. Here, we discuss results from combined microscopic and genomic approaches that directly connect micronucleus fate with chromoanagenesis. The major methods of investigation that allowed to identify the origin of chromoanagenesis from micronuclei are also presented.

摘要

染色体骤变定义了一组高度复杂的染色体重排,这些重排局限于单个或少数几条染色体,据推测是在一次灾难性事件中发生的。多项实验结果已将染色体骤变与微核的形成联系起来,微核是含有错分染色体或染色体片段的小核外染色质结构。实验证据表明,微核周围包膜的内在脆弱性是膜破裂的原因。因此,微核DNA会暴露于各种细胞质活动中,从而产生染色体骤变特有的局部多处断裂模式。在此,我们讨论了结合显微镜和基因组方法得出的结果,这些结果直接将微核命运与染色体骤变联系起来。还介绍了能够确定微核引发染色体骤变起源的主要研究方法。

相似文献

[1]
Origin and Fate of Micronuclei on the Road to Chromoanagenesis.

Methods Mol Biol. 2025

[2]
Transcription-Replication Conflicts and Incomplete Replication as a Cause of Micronuclei-Driven Chromoanagenesis.

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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Micronuclei induced by radiation, replication stress, or chromosome segregation errors do not activate cGAS-STING.

Mol Cell. 2024-6-6

[2]
The proteomic landscape of genotoxic stress-induced micronuclei.

Mol Cell. 2024-4-4

[3]
Induction of chromosome-specific micronuclei and chromothripsis by centromere inactivation.

Methods Cell Biol. 2024

[4]
Boveri and beyond: Chromothripsis and genomic instability from mitotic errors.

Mol Cell. 2024-1-4

[5]
Scrambling the genome in cancer: causes and consequences of complex chromosome rearrangements.

Nat Rev Genet. 2024-3

[6]
ATR promotes clearance of damaged DNA and damaged cells by rupturing micronuclei.

Mol Cell. 2023-10-19

[7]
Centromere: A Trojan horse for genome stability.

DNA Repair (Amst). 2023-10

[8]
Heritable transcriptional defects from aberrations of nuclear architecture.

Nature. 2023-7

[9]
Epigenetic dysregulation from chromosomal transit in micronuclei.

Nature. 2023-7

[10]
Nucleophagy contributes to genome stability through degradation of type II topoisomerases A and B and nucleolar components.

J Cell Sci. 2023-1-1

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