The Nuclear Pore Complex: Birth, Life, and Death of a Cellular Behemoth

被引:32
作者
Dultz, Elisa [1 ]
Wojtynek, Matthias [1 ,2 ]
Medalia, Ohad [2 ]
Onischenko, Evgeny [3 ]
机构
[1] ETHZ Zurich, Inst Biochem, Dept Biol, CH-8093 Zurich, Switzerland
[2] Univ Zurich, Dept Biochem, CH-8057 Zurich, Switzerland
[3] Univ Bergen, Dept Biol Sci, N-5020 Bergen, Norway
关键词
nuclear pore complex; nucleoporin; NPC; membrane fusion; Ran; lipids; assembly factor; amphipathic helix; nuclear transport receptor; FG repeats; Brl1; autophagy; ageing; aggregation; neurodegneration; MESSENGER-RNA EXPORT; SCANNING-ELECTRON-MICROSCOPY; SELECTIVE AUTOPHAGY DEGRADES; NUCLEOCYTOPLASMIC TRANSPORT; MEMBRANE-PROTEINS; QUALITY-CONTROL; BUDDING YEAST; RAN GTPASE; MULTIPROTEIN COMPLEX; STRUCTURAL-ANALYSIS;
D O I
10.3390/cells11091456
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Nuclear pore complexes (NPCs) are the only transport channels that cross the nuclear envelope. Constructed from similar to 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.
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