Howard Hughes Medical Institute, Chevy Chase, MD, USA.
Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
Nucleus. 2020 Dec;11(1):35-52. doi: 10.1080/19491034.2020.1742064.
The nuclear envelope (NE) is composed of two lipid bilayer membranes that enclose the eukaryotic genome. In interphase, the NE is perforated by thousands of nuclear pore complexes (NPCs), which allow transport in and out of the nucleus. During mitosis in metazoans, the NE is broken down and then reassembled in a manner that enables proper chromosome segregation and the formation of a single nucleus in each daughter cell. Defects in coordinating NE reformation and chromosome segregation can cause aberrant nuclear architecture. This includes the formation of micronuclei, which can trigger a catastrophic mutational process commonly observed in cancers called chromothripsis. Here, we discuss the current understanding of the coordination of NE reformation with chromosome segregation during mitotic exit in metazoans. We review differing models in the field and highlight recent work suggesting that normal NE reformation and chromosome segregation are physically linked through the timing of mitotic spindle disassembly.
核膜(NE)由两个脂质双分子层组成,包围着真核基因组。在间期中,NE 上有数千个核孔复合物(NPC)穿孔,允许核内外物质的运输。在真核生物的有丝分裂过程中,NE 被分解,然后以一种能够正确分离染色体并在每个子细胞中形成单个核的方式重新组装。协调 NE 重建和染色体分离的缺陷会导致异常的核结构。这包括微核的形成,微核可能会引发一种称为染色体重排的癌症中常见的灾难性突变过程。在这里,我们讨论了目前对真核生物有丝分裂后期 NE 重建与染色体分离协调的理解。我们回顾了该领域的不同模型,并强调了最近的工作,表明正常的 NE 重建和染色体分离通过有丝分裂纺锤体解体的时间在物理上是相关联的。