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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...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2009
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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. |
format | Text |
id | pubmed-2731110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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