Institute of Biochemistry, Department of Biology, ETHZ Zurich, 8093 Zurich, Switzerland.
Department of Biochemistry, University of Zurich, 8057 Zurich, Switzerland.
Cells. 2022 Apr 25;11(9):1456. doi: 10.3390/cells11091456.
Nuclear pore complexes (NPCs) are the only transport channels that cross the nuclear envelope. Constructed from ~500-1000 nucleoporin proteins each, they are among the largest macromolecular assemblies in eukaryotic cells. Thanks to advances in structural analysis approaches, the construction principles and architecture of the NPC have recently been revealed at submolecular resolution. Although the overall structure and inventory of nucleoporins are conserved, NPCs exhibit significant compositional and functional plasticity even within single cells and surprising variability in their assembly pathways. Once assembled, NPCs remain seemingly unexchangeable in post-mitotic cells. There are a number of as yet unresolved questions about how the versatility of NPC assembly and composition is established, how cells monitor the functional state of NPCs or how they could be renewed. Here, we review current progress in our understanding of the key aspects of NPC architecture and lifecycle.
核孔复合体(NPC)是唯一穿过核膜的运输通道。每个 NPC 由约 500-1000 个核孔蛋白组成,是真核细胞中最大的大分子组装体之一。得益于结构分析方法的进步,NPC 的构建原则和结构最近已在亚分子分辨率下揭示。尽管核孔蛋白的整体结构和成分是保守的,但 NPC 即使在单个细胞内也表现出显著的组成和功能可塑性,其组装途径也存在惊人的可变性。一旦组装完成,NPC 在有丝分裂后细胞中似乎是不可交换的。关于 NPC 组装和组成的多功能性是如何建立的、细胞如何监测 NPC 的功能状态或它们如何被更新,仍有许多悬而未决的问题。在这里,我们回顾了目前对 NPC 结构和生命周期关键方面的理解进展。