Literature DB >> 10813398

The nuclear pore complex: structure, function, and dynamics.

E Kiseleva1, M W Goldberg, J Cronshaw, T D Allen.   

Abstract

A full understanding of nucleocytoplasmic transport depends on knowledge of nuclear pore complex (NPC) structure, the functional roles of NPC components, their interactions during transport and dynamics during the cell cycle. NPC structure is conserved, flexible, and is not simply a tunnel between the nucleus and cytoplasm but appears to be actively involved in the transport process by a series of structural modifications. Transport through the NPC begins in either of its asymmetrical peripheral compartments that are both structurally reorganized during transport in different ways. The central compartment is composed of two symmetrical halves, and functions as a system of transiently open, discrete gates that is not believed to play a role in determining direction. Each NPC subunit has a specific morphology that corresponds to the functional role it plays. A complicated system of vertical and horizontal connections may allow one part of the NPC to transmit a signal to other parts, leading to an ordered series of conformational changes that drive translocation. High-resolution scanning electron microscopy has identified sequential stages of NPC assembly in vitro and revealed how the individual NPC components are assembled into a mature NPC. This review focuses on structural events during transport and on possible mechanisms of NPC assembly.

Mesh:

Year:  2000        PMID: 10813398

Source DB:  PubMed          Journal:  Crit Rev Eukaryot Gene Expr        ISSN: 1045-4403            Impact factor:   1.807


  12 in total

1.  Kinetics and mechanism of DNA uptake into the cell nucleus.

Authors:  H Salman; D Zbaida; Y Rabin; D Chatenay; M Elbaum
Journal:  Proc Natl Acad Sci U S A       Date:  2001-06-05       Impact factor: 11.205

2.  Regulation of nuclear pore complex conformation by IP(3) receptor activation.

Authors:  David Moore-Nichols; Anne Arnott; Robert C Dunn
Journal:  Biophys J       Date:  2002-09       Impact factor: 4.033

3.  Disruption of the FG nucleoporin NUP98 causes selective changes in nuclear pore complex stoichiometry and function.

Authors:  X Wu; L H Kasper; R T Mantcheva; G T Mantchev; M J Springett; J M van Deursen
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-13       Impact factor: 11.205

4.  SUN1 interacts with nuclear lamin A and cytoplasmic nesprins to provide a physical connection between the nuclear lamina and the cytoskeleton.

Authors:  Farhana Haque; David J Lloyd; Dawn T Smallwood; Carolyn L Dent; Catherine M Shanahan; Andrew M Fry; Richard C Trembath; Sue Shackleton
Journal:  Mol Cell Biol       Date:  2006-05       Impact factor: 4.272

5.  Model system to study classical nuclear export signals.

Authors:  Charu Kanwal; Henan Li; Carol S Lim
Journal:  AAPS PharmSci       Date:  2002

6.  Integrase interacts with nucleoporin NUP153 to mediate the nuclear import of human immunodeficiency virus type 1.

Authors:  Cora L Woodward; Sarin Prakobwanakit; Sherly Mosessian; Samson A Chow
Journal:  J Virol       Date:  2009-04-15       Impact factor: 5.103

Review 7.  The nuclear pore complex has entered the atomic age.

Authors:  Stephen G Brohawn; James R Partridge; James R R Whittle; Thomas U Schwartz
Journal:  Structure       Date:  2009-09-09       Impact factor: 5.006

8.  The two tempos of nuclear pore complex evolution: highly adapting proteins in an ancient frozen structure.

Authors:  Eric Bapteste; Robert L Charlebois; Dave MacLeod; Céline Brochier
Journal:  Genome Biol       Date:  2005-09-30       Impact factor: 13.583

9.  Xenopus importin beta validates human importin beta as a cell cycle negative regulator.

Authors:  Valerie A Delmar; Rene C Chan; Douglass J Forbes
Journal:  BMC Cell Biol       Date:  2008-03-22       Impact factor: 4.241

10.  Transcriptional elongation and mRNA export are coregulated processes.

Authors:  Maria Micaela Molina-Navarro; Celia Pilar Martinez-Jimenez; Susana Rodriguez-Navarro
Journal:  Genet Res Int       Date:  2011-10-05
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