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Dynamic localisation of Ran GTPase during the cell cycle

BACKGROUND: Ran GTPase has multiple functions during the cell division cycle, including nucleocytoplasmic transport, mitotic spindle assembly and nuclear envelope formation. The activity of Ran is determined by both its guanine nucleotide-bound state and its subcellular localization. RESULTS: Here,...

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Autores principales: Hutchins, James RA, Moore, William J, Clarke, Paul R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2755469/
https://www.ncbi.nlm.nih.gov/pubmed/19765287
http://dx.doi.org/10.1186/1471-2121-10-66
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author Hutchins, James RA
Moore, William J
Clarke, Paul R
author_facet Hutchins, James RA
Moore, William J
Clarke, Paul R
author_sort Hutchins, James RA
collection PubMed
description BACKGROUND: Ran GTPase has multiple functions during the cell division cycle, including nucleocytoplasmic transport, mitotic spindle assembly and nuclear envelope formation. The activity of Ran is determined by both its guanine nucleotide-bound state and its subcellular localization. RESULTS: Here, we have characterised the localisation and mobility of Ran coupled to green fluorescent protein (GFP) during the cell cycle in live human cells. Ran-GFP is nuclear during interphase and is dispersed throughout the cell during mitosis. GFP-Ran(Q69L), a mutant locked in the GTP-bound state, is less highly concentrated in the nucleus and associates with nuclear pore complexes within the nuclear envelope. During mitosis, GFP-Ran(Q69L )is excluded from chromosomes and localizes to the spindle. By contrast, GFP-Ran(T24N), a mutant with low affinity for nucleotides, interacts relatively stably with chromatin throughout the cell cycle and is highly concentrated on mitotic chromosomes. CONCLUSION: These results show that Ran interacts dynamically with chromatin, nuclear pore complexes and the mitotic spindle during the cell cycle. These interactions are dependent on the nucleotide-bound state of the protein. Our data indicate that Ran-GTP generated at chromatin is highly mobile and interacts dynamically with distal structures that are involved in nuclear transport and mitotic spindle assembly.
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spelling pubmed-27554692009-10-02 Dynamic localisation of Ran GTPase during the cell cycle Hutchins, James RA Moore, William J Clarke, Paul R BMC Cell Biol Research Article BACKGROUND: Ran GTPase has multiple functions during the cell division cycle, including nucleocytoplasmic transport, mitotic spindle assembly and nuclear envelope formation. The activity of Ran is determined by both its guanine nucleotide-bound state and its subcellular localization. RESULTS: Here, we have characterised the localisation and mobility of Ran coupled to green fluorescent protein (GFP) during the cell cycle in live human cells. Ran-GFP is nuclear during interphase and is dispersed throughout the cell during mitosis. GFP-Ran(Q69L), a mutant locked in the GTP-bound state, is less highly concentrated in the nucleus and associates with nuclear pore complexes within the nuclear envelope. During mitosis, GFP-Ran(Q69L )is excluded from chromosomes and localizes to the spindle. By contrast, GFP-Ran(T24N), a mutant with low affinity for nucleotides, interacts relatively stably with chromatin throughout the cell cycle and is highly concentrated on mitotic chromosomes. CONCLUSION: These results show that Ran interacts dynamically with chromatin, nuclear pore complexes and the mitotic spindle during the cell cycle. These interactions are dependent on the nucleotide-bound state of the protein. Our data indicate that Ran-GTP generated at chromatin is highly mobile and interacts dynamically with distal structures that are involved in nuclear transport and mitotic spindle assembly. BioMed Central 2009-09-18 /pmc/articles/PMC2755469/ /pubmed/19765287 http://dx.doi.org/10.1186/1471-2121-10-66 Text en Copyright © 2009 Hutchins et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hutchins, James RA
Moore, William J
Clarke, Paul R
Dynamic localisation of Ran GTPase during the cell cycle
title Dynamic localisation of Ran GTPase during the cell cycle
title_full Dynamic localisation of Ran GTPase during the cell cycle
title_fullStr Dynamic localisation of Ran GTPase during the cell cycle
title_full_unstemmed Dynamic localisation of Ran GTPase during the cell cycle
title_short Dynamic localisation of Ran GTPase during the cell cycle
title_sort dynamic localisation of ran gtpase during the cell cycle
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2755469/
https://www.ncbi.nlm.nih.gov/pubmed/19765287
http://dx.doi.org/10.1186/1471-2121-10-66
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