| Literature DB >> 34129835 |
Yi-Ying Chou1, Srigokul Upadhyayula2, Justin Houser3, Kangmin He4, Wesley Skillern3, Gustavo Scanavachi5, Song Dang3, Anwesha Sanyal1, Kazuka G Ohashi3, Giuseppe Di Caprio6, Alex J B Kreutzberger1, Tegy John Vadakkan3, Tom Kirchhausen7.
Abstract
Nuclear envelope assembly during late mitosis includes rapid formation of several thousand complete nuclear pore complexes (NPCs). This efficient use of NPC components (nucleoporins or "NUPs") is essential for ensuring immediate nucleocytoplasmic communication in each daughter cell. We show that octameric subassemblies of outer and inner nuclear pore rings remain intact in the mitotic endoplasmic reticulum (ER) after NPC disassembly during prophase. These "inherited" subassemblies then incorporate into NPCs during post-mitotic pore formation. We further show that the stable subassemblies persist through multiple rounds of cell division and the accompanying rounds of NPC mitotic disassembly and post-mitotic assembly. De novo formation of NPCs from newly synthesized NUPs during interphase will then have a distinct initiation mechanism. We postulate that a yet-to-be-identified modification marks and "immortalizes" one or more components of the specific octameric outer and inner ring subcomplexes that then template post-mitotic NPC assembly during subsequent cell cycles.Entities:
Keywords: FIB-SEM; cell division; endoplasmic reticulum; inheritance; lattice light-sheet microscopy; live cell imaging; mitosis; nuclear envelope; nuclear pore complex; spinning disk confocal microscopy
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Year: 2021 PMID: 34129835 PMCID: PMC8261643 DOI: 10.1016/j.devcel.2021.05.015
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 13.417