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The RanGTP Pathway: From Nucleo-Cytoplasmic Transport to Spindle Assembly and Beyond
The small GTPase Ran regulates the interaction of transport receptors with a number of cellular cargo proteins. The high affinity binding of the GTP-bound form of Ran to import receptors promotes cargo release, whereas its binding to export receptors stabilizes their interaction with the cargo. This...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707252/ https://www.ncbi.nlm.nih.gov/pubmed/26793706 http://dx.doi.org/10.3389/fcell.2015.00082 |
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author | Cavazza, Tommaso Vernos, Isabelle |
author_facet | Cavazza, Tommaso Vernos, Isabelle |
author_sort | Cavazza, Tommaso |
collection | PubMed |
description | The small GTPase Ran regulates the interaction of transport receptors with a number of cellular cargo proteins. The high affinity binding of the GTP-bound form of Ran to import receptors promotes cargo release, whereas its binding to export receptors stabilizes their interaction with the cargo. This basic mechanism linked to the asymmetric distribution of the two nucleotide-bound forms of Ran between the nucleus and the cytoplasm generates a switch like mechanism controlling nucleo-cytoplasmic transport. Since 1999, we have known that after nuclear envelope breakdown (NEBD) Ran and the above transport receptors also provide a local control over the activity of factors driving spindle assembly and regulating other aspects of cell division. The identification and functional characterization of RanGTP mitotic targets is providing novel insights into mechanisms essential for cell division. Here we review our current knowledge on the RanGTP system and its regulation and we focus on the recent advances made through the characterization of its mitotic targets. We then briefly review the novel functions of the pathway that were recently described. Altogether, the RanGTP system has moonlighting functions exerting a spatial control over protein interactions that drive specific functions depending on the cellular context. |
format | Online Article Text |
id | pubmed-4707252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47072522016-01-20 The RanGTP Pathway: From Nucleo-Cytoplasmic Transport to Spindle Assembly and Beyond Cavazza, Tommaso Vernos, Isabelle Front Cell Dev Biol Cell and Developmental Biology The small GTPase Ran regulates the interaction of transport receptors with a number of cellular cargo proteins. The high affinity binding of the GTP-bound form of Ran to import receptors promotes cargo release, whereas its binding to export receptors stabilizes their interaction with the cargo. This basic mechanism linked to the asymmetric distribution of the two nucleotide-bound forms of Ran between the nucleus and the cytoplasm generates a switch like mechanism controlling nucleo-cytoplasmic transport. Since 1999, we have known that after nuclear envelope breakdown (NEBD) Ran and the above transport receptors also provide a local control over the activity of factors driving spindle assembly and regulating other aspects of cell division. The identification and functional characterization of RanGTP mitotic targets is providing novel insights into mechanisms essential for cell division. Here we review our current knowledge on the RanGTP system and its regulation and we focus on the recent advances made through the characterization of its mitotic targets. We then briefly review the novel functions of the pathway that were recently described. Altogether, the RanGTP system has moonlighting functions exerting a spatial control over protein interactions that drive specific functions depending on the cellular context. Frontiers Media S.A. 2016-01-11 /pmc/articles/PMC4707252/ /pubmed/26793706 http://dx.doi.org/10.3389/fcell.2015.00082 Text en Copyright © 2016 Cavazza and Vernos. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Cavazza, Tommaso Vernos, Isabelle The RanGTP Pathway: From Nucleo-Cytoplasmic Transport to Spindle Assembly and Beyond |
title | The RanGTP Pathway: From Nucleo-Cytoplasmic Transport to Spindle Assembly and Beyond |
title_full | The RanGTP Pathway: From Nucleo-Cytoplasmic Transport to Spindle Assembly and Beyond |
title_fullStr | The RanGTP Pathway: From Nucleo-Cytoplasmic Transport to Spindle Assembly and Beyond |
title_full_unstemmed | The RanGTP Pathway: From Nucleo-Cytoplasmic Transport to Spindle Assembly and Beyond |
title_short | The RanGTP Pathway: From Nucleo-Cytoplasmic Transport to Spindle Assembly and Beyond |
title_sort | rangtp pathway: from nucleo-cytoplasmic transport to spindle assembly and beyond |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707252/ https://www.ncbi.nlm.nih.gov/pubmed/26793706 http://dx.doi.org/10.3389/fcell.2015.00082 |
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