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Nucleocytoplasmic transport of Alp7/TACC organizes spatiotemporal microtubule formation in fission yeast

Ran GTPase activates several target molecules to induce microtubule formation around the chromosomes and centrosomes. In fission yeast, in which the nuclear envelope does not break down during mitosis, Ran targets the centrosomal transforming acidic coiled-coil (TACC) protein Alp7 for spindle format...

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Autores principales: Sato, Masamitsu, Okada, Naoyuki, Kakui, Yasutaka, Yamamoto, Masayuki, Yoshida, Minoru, Toda, Takashi
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2731110/
https://www.ncbi.nlm.nih.gov/pubmed/19696784
http://dx.doi.org/10.1038/embor.2009.158
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author Sato, Masamitsu
Okada, Naoyuki
Kakui, Yasutaka
Yamamoto, Masayuki
Yoshida, Minoru
Toda, Takashi
author_facet Sato, Masamitsu
Okada, Naoyuki
Kakui, Yasutaka
Yamamoto, Masayuki
Yoshida, Minoru
Toda, Takashi
author_sort Sato, Masamitsu
collection PubMed
description Ran GTPase activates several target molecules to induce microtubule formation around the chromosomes and centrosomes. In fission yeast, in which the nuclear envelope does not break down during mitosis, Ran targets the centrosomal transforming acidic coiled-coil (TACC) protein Alp7 for spindle formation. Alp7 accumulates in the nucleus only during mitosis, although its underlying mechanism remains elusive. Here, we investigate the behaviour of Alp7 and its binding partner, Alp14/TOG, throughout the cell cycle. Interestingly, Alp7 enters the nucleus during interphase but is subsequently exported to the cytoplasm by the Exportin-dependent nuclear export machinery. The continuous nuclear export of Alp7 during interphase is essential for maintaining the array-like cytoplasmic microtubule structure. The mitosis-specific nuclear accumulation of Alp7 seems to be under the control of cyclin-dependent kinase (CDK). These results indicate that the spatiotemporal regulation of microtubule formation is established by the Alp7/TACC–Alp14/TOG complex through the coordinated interplay of Ran and CDK.
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spelling pubmed-27311102009-09-02 Nucleocytoplasmic transport of Alp7/TACC organizes spatiotemporal microtubule formation in fission yeast Sato, Masamitsu Okada, Naoyuki Kakui, Yasutaka Yamamoto, Masayuki Yoshida, Minoru Toda, Takashi EMBO Rep Scientific Report Ran GTPase activates several target molecules to induce microtubule formation around the chromosomes and centrosomes. In fission yeast, in which the nuclear envelope does not break down during mitosis, Ran targets the centrosomal transforming acidic coiled-coil (TACC) protein Alp7 for spindle formation. Alp7 accumulates in the nucleus only during mitosis, although its underlying mechanism remains elusive. Here, we investigate the behaviour of Alp7 and its binding partner, Alp14/TOG, throughout the cell cycle. Interestingly, Alp7 enters the nucleus during interphase but is subsequently exported to the cytoplasm by the Exportin-dependent nuclear export machinery. The continuous nuclear export of Alp7 during interphase is essential for maintaining the array-like cytoplasmic microtubule structure. The mitosis-specific nuclear accumulation of Alp7 seems to be under the control of cyclin-dependent kinase (CDK). These results indicate that the spatiotemporal regulation of microtubule formation is established by the Alp7/TACC–Alp14/TOG complex through the coordinated interplay of Ran and CDK. Nature Publishing Group 2009-10 2009-08-21 /pmc/articles/PMC2731110/ /pubmed/19696784 http://dx.doi.org/10.1038/embor.2009.158 Text en Copyright © 2009, European Molecular Biology Organization http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits distribution, and reproduction in any medium, provided the original author and source are credited. This license does not permit commercial exploitation without specific permission.
spellingShingle Scientific Report
Sato, Masamitsu
Okada, Naoyuki
Kakui, Yasutaka
Yamamoto, Masayuki
Yoshida, Minoru
Toda, Takashi
Nucleocytoplasmic transport of Alp7/TACC organizes spatiotemporal microtubule formation in fission yeast
title Nucleocytoplasmic transport of Alp7/TACC organizes spatiotemporal microtubule formation in fission yeast
title_full Nucleocytoplasmic transport of Alp7/TACC organizes spatiotemporal microtubule formation in fission yeast
title_fullStr Nucleocytoplasmic transport of Alp7/TACC organizes spatiotemporal microtubule formation in fission yeast
title_full_unstemmed Nucleocytoplasmic transport of Alp7/TACC organizes spatiotemporal microtubule formation in fission yeast
title_short Nucleocytoplasmic transport of Alp7/TACC organizes spatiotemporal microtubule formation in fission yeast
title_sort nucleocytoplasmic transport of alp7/tacc organizes spatiotemporal microtubule formation in fission yeast
topic Scientific Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2731110/
https://www.ncbi.nlm.nih.gov/pubmed/19696784
http://dx.doi.org/10.1038/embor.2009.158
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