Journal Article10.1242/JCS.106.1.261
The nuclear pore complex : three-dimensional surface structure revealed by field emission, in-lens scanning electron microscopy, with underlying structure uncovered by proteolysis
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TL;DR: It is determined that the nucleoplasmic filaments that make up the baskets are attached to the outer periphery of the coaxial ring at a position between each of its subunits, consistent with the exclusion limit previously found for NPC-transported molecules.
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Abstract: The structure of the nuclear pore complex (NPC) has been previously studied by many different electron microscopic techniques. Recently, scanning electron microscopes have been developed that can visualise biologically relevant structural detail at the same level of resolution as transmission electron microscopes and have been used to study NPC structure. We have used such an instrument to visualise directly the structure of both cytoplasmic and nucleoplasmic surfaces of the NPC of manually isolated amphibian oocyte nuclear envelopes that have been spread, fixed, critical point dried and coated with a thin fine-grained film of chromium or tantalum. We present images that directly show features of the NPC that are visible at each surface, including coaxial rings, cytoplasmic particles, plug/spoke complexes and the nucleoplasmic basket or fishtrap. Some cytoplasmic particles are rod-shaped or possibly "T"-shaped, can be quite long structures extending into the cytoplasm and may be joined to the coaxial ring at a position between each subunit. Both coaxial rings, which are proud of the membranes, can be exposed by light proteolytic digestion, revealing eight equal subunits each of which may be bipartite. We have determined that the nucleoplasmic filaments that make up the baskets are attached to the outer periphery of the coaxial ring at a position between each of its subunits. These filaments extend into the nucleoplasm and insert at the distal end to the smaller basket ring. The space left between adjacent basket filaments would exclude particles bigger than about 25 nm, which is consistent with the exclusion limit previously found for NPC-transported molecules.
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A novel nuclear pore protein Nup133p with distinct roles in poly(A)+ RNA transport and nuclear pore distribution.
TL;DR: Temperature‐sensitive nucleoporin nup49‐316 mutant cells accumulate poly(A)+ RNA inside the nucleus when shifted to restrictive temperature, and the nuclear pore clustering phenotype and intranuclear accumulation of poly( A)+ RNA are not obligatorily linked.
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The cytoplasmic filaments of the nuclear pore complex are dispensable for selective nuclear protein import
Tobias C. Walther,Helen Pickersgill,Volker C. Cordes,Martin W. Goldberg,T. D. Allen,Iain W. Mattaj,Maarten Fornerod,Maarten Fornerod +7 more
TL;DR: It is concluded that RanBP2 is the major nucleoporin component of the cytoplasmic filaments of the NPC, and that these filaments do not have an essential role in importin α/β– or transportin-dependent import.
Dimples, pores, star-rings, and thin rings on growing nuclear envelopes: evidence for structural intermediates in nuclear pore complex assembly
TL;DR: It is proposed that assembly begins with the formation and stabilization of a hole (pore) through the nuclear envelope, and that dimples, pores, star-rings, and thin rings are structural intermediates in nuclear pore complex assembly.
Herpes Simplex Virus Replication: Roles of Viral Proteins and Nucleoporins in Capsid-Nucleus Attachment
TL;DR: Results are interpreted to suggest that VP1/2 is involved in specific attachment to the NPC and/or in migration of capsids to the nuclear surface, with high-resolution immunofluorescence studies favoring binding to Nup358.
175
References
Glycosylation in the nucleus and cytoplasm
TL;DR: The role of lectin binding sites in the Nucleus, as well as other mechanisms, are investigated in more detail in the next chapter.
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The nuclear envelope and the architecture of the nuclear periphery
TL;DR: Several authors noted the plasticity and viscosity of the nuclear membrane, properties that were critically discussed by Flemming (2), who correctly pointed to the lack of evidence for the existence of such pores.
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High resolution scanning electron microscopy of the nuclear envelope: demonstration of a new, regular, fibrous lattice attached to the baskets of the nucleoplasmic face of the nuclear pores.
TL;DR: The use of HRSEM is demonstrated to obtain high resolution information of NE structure, confirming previous data and providing some new information about the nuclear envelope of amphibian oocytes.
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Visualization of transport-related configurations of the nuclear pore transporter
TL;DR: Data confirms previous observations on NPC transporters labeled with nucleoplasmin-gold and allows a working model of the central NPC transporter to be proposed, comprised of two supramolecular irislike assemblies which open asynchronously to provide an expanded pore for translocation while maintaining transport fidelity.
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