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Dissecting in vivo steady-state dynamics of karyopherin-dependent nuclear transport

Karyopherin-dependent molecular transport through the nuclear pore complex is maintained by constant recycling pathways of karyopherins coupled with the Ran-dependent cargo catch-and-release mechanism. Although many studies have revealed the bidirectional dynamics of karyopherins, the entire kinetic...

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Autores principales: Lolodi, Ogheneochukome, Yamazaki, Hiroya, Otsuka, Shotaro, Kumeta, Masahiro, Yoshimura, Shige H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694755/
https://www.ncbi.nlm.nih.gov/pubmed/26538027
http://dx.doi.org/10.1091/mbc.E15-08-0601
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author Lolodi, Ogheneochukome
Yamazaki, Hiroya
Otsuka, Shotaro
Kumeta, Masahiro
Yoshimura, Shige H.
author_facet Lolodi, Ogheneochukome
Yamazaki, Hiroya
Otsuka, Shotaro
Kumeta, Masahiro
Yoshimura, Shige H.
author_sort Lolodi, Ogheneochukome
collection PubMed
description Karyopherin-dependent molecular transport through the nuclear pore complex is maintained by constant recycling pathways of karyopherins coupled with the Ran-dependent cargo catch-and-release mechanism. Although many studies have revealed the bidirectional dynamics of karyopherins, the entire kinetics of the steady-state dynamics of karyopherin and cargo is still not fully understood. In this study, we used fluorescence recovery after photobleaching and fluorescence loss in photobleaching on live cells to provide convincing in vivo proof that karyopherin-mediated nucleocytoplasmic transport of cargoes is bidirectional. Continuous photobleaching of the cytoplasm of live cells expressing NLS cargoes led to progressive decrease of nuclear fluorescence signals. In addition, experimentally obtained kinetic parameters of karyopherin complexes were used to establish a kinetic model to explain the entire cargo import and export transport cycles facilitated by importin β. The results strongly indicate that constant shuttling of karyopherins, either free or bound to cargo, ensures proper balancing of nucleocytoplasmic distribution of cargoes and establishes effective regulation of cargo dynamics by RanGTP.
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spelling pubmed-46947552016-03-16 Dissecting in vivo steady-state dynamics of karyopherin-dependent nuclear transport Lolodi, Ogheneochukome Yamazaki, Hiroya Otsuka, Shotaro Kumeta, Masahiro Yoshimura, Shige H. Mol Biol Cell Articles Karyopherin-dependent molecular transport through the nuclear pore complex is maintained by constant recycling pathways of karyopherins coupled with the Ran-dependent cargo catch-and-release mechanism. Although many studies have revealed the bidirectional dynamics of karyopherins, the entire kinetics of the steady-state dynamics of karyopherin and cargo is still not fully understood. In this study, we used fluorescence recovery after photobleaching and fluorescence loss in photobleaching on live cells to provide convincing in vivo proof that karyopherin-mediated nucleocytoplasmic transport of cargoes is bidirectional. Continuous photobleaching of the cytoplasm of live cells expressing NLS cargoes led to progressive decrease of nuclear fluorescence signals. In addition, experimentally obtained kinetic parameters of karyopherin complexes were used to establish a kinetic model to explain the entire cargo import and export transport cycles facilitated by importin β. The results strongly indicate that constant shuttling of karyopherins, either free or bound to cargo, ensures proper balancing of nucleocytoplasmic distribution of cargoes and establishes effective regulation of cargo dynamics by RanGTP. The American Society for Cell Biology 2016-01-01 /pmc/articles/PMC4694755/ /pubmed/26538027 http://dx.doi.org/10.1091/mbc.E15-08-0601 Text en © 2016 Lolodi et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.
spellingShingle Articles
Lolodi, Ogheneochukome
Yamazaki, Hiroya
Otsuka, Shotaro
Kumeta, Masahiro
Yoshimura, Shige H.
Dissecting in vivo steady-state dynamics of karyopherin-dependent nuclear transport
title Dissecting in vivo steady-state dynamics of karyopherin-dependent nuclear transport
title_full Dissecting in vivo steady-state dynamics of karyopherin-dependent nuclear transport
title_fullStr Dissecting in vivo steady-state dynamics of karyopherin-dependent nuclear transport
title_full_unstemmed Dissecting in vivo steady-state dynamics of karyopherin-dependent nuclear transport
title_short Dissecting in vivo steady-state dynamics of karyopherin-dependent nuclear transport
title_sort dissecting in vivo steady-state dynamics of karyopherin-dependent nuclear transport
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694755/
https://www.ncbi.nlm.nih.gov/pubmed/26538027
http://dx.doi.org/10.1091/mbc.E15-08-0601
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