Understanding the birth of rupture-prone and irreparable micronuclei

被引:28
作者
Guo, Xihan [1 ]
Dai, Xueqin [2 ,3 ,4 ]
Wu, Xue [1 ]
Zhou, Tao [1 ]
Ni, Juan [1 ]
Xue, Jinglun [5 ]
Wang, Xu [1 ]
机构
[1] Yunnan Normal Univ, Engn Res Ctr Sustainable Dev & Utilizat Biomass E, Sch Life Sci, Kunming 650500, Yunnan, Peoples R China
[2] Chinese Acad Sci, Kunming Inst Zool, State Key Lab Genet Resources & Evolut, Kunming 650223, Yunnan, Peoples R China
[3] Univ Chinese Acad Sci, Kunming Coll Life Sci, Kunming 650204, Yunnan, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[5] Fudan Univ, Inst Genet, Sch Life Sci, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
Micronuclei; Lagging chromosomes; Nuclear envelope reassemble; Nuclear envelope rupture; Chromothripsis; cGAS-STING pathway; NUCLEAR-ENVELOPE RUPTURE; AURORA-B; DNA-DAMAGE; ABSCISSION CHECKPOINT; CHROMOSOME SEPARATION; LAGGING CHROMOSOMES; ESCRT-III; CELLS; DEGRADATION; REPAIR;
D O I
10.1007/s00412-020-00741-w
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Micronuclei are extra-nuclear bodies mainly derived from ana-telophase lagging chromosomes/chromatins (LCs) that are not incorporated into primary nuclei at mitotic exit. Unlike primary nuclei, most micronuclei are enclosed by nuclear envelope (NE) that is highly susceptible to spontaneous and irreparable rupture. Ruptured micronuclei act as triggers of chromothripsis-like chaotic chromosomal rearrangements and cGAS-mediated innate immunity and inflammation, raising the view that micronuclei play active roles in human aging and tumorigenesis. Thus, understanding the ways in which micronuclear envelope (mNE) goes awry acquires increased importance. Here, we review the data to present a general framework for this question. We firstly describe NE reassembly after mitosis and NE repair during interphase. Simultaneously, we briefly discuss how mNE is organized and how mNE rupture controls the fate of micronuclei and micronucleated cells. As a focus of this review, we highlight current knowledge about why mNE is rupture-prone and irreparable. For this, we survey observations from a series of elegant studies to provide a systematic overview. We conclude that the birth of rupture-prone and irreparable micronuclei may be the cumulative effects of their intracellular geographic origins, biophysical properties, and specific mNE features. We propose that DNA damage and immunogenicity in micronuclei increase stepwise from altered mNE components, mNE rupture, and refractory to repair. Throughout our discussion, we note interesting issues in mNE fragility that have yet to be resolved.
引用
收藏
页码:181 / 200
页数:20
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