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NuSAP, a novel microtubule-associated protein involved in mitotic spindle organization
Here, we report on the identification of nucleolar spindle–associated protein (NuSAP), a novel 55-kD vertebrate protein with selective expression in proliferating cells. Its mRNA and protein levels peak at the transition of G2 to mitosis and abruptly decline after cell division. Microscopic analysis...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172854/ https://www.ncbi.nlm.nih.gov/pubmed/12963707 http://dx.doi.org/10.1083/jcb.200302129 |
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author | Raemaekers, Tim Ribbeck, Katharina Beaudouin, Joël Annaert, Wim Van Camp, Mark Stockmans, Ingrid Smets, Nico Bouillon, Roger Ellenberg, Jan Carmeliet, Geert |
author_facet | Raemaekers, Tim Ribbeck, Katharina Beaudouin, Joël Annaert, Wim Van Camp, Mark Stockmans, Ingrid Smets, Nico Bouillon, Roger Ellenberg, Jan Carmeliet, Geert |
author_sort | Raemaekers, Tim |
collection | PubMed |
description | Here, we report on the identification of nucleolar spindle–associated protein (NuSAP), a novel 55-kD vertebrate protein with selective expression in proliferating cells. Its mRNA and protein levels peak at the transition of G2 to mitosis and abruptly decline after cell division. Microscopic analysis of both fixed and live mammalian cells showed that NuSAP is primarily nucleolar in interphase, and localizes prominently to central spindle microtubules during mitosis. Direct interaction of NuSAP with microtubules was demonstrated in vitro. Overexpression of NuSAP caused profound bundling of cytoplasmic microtubules in interphase cells, and this relied on a COOH-terminal microtubule-binding domain. In contrast, depletion of NuSAP by RNA interference resulted in aberrant mitotic spindles, defective chromosome segregation, and cytokinesis. In addition, many NuSAP-depleted interphase cells had deformed nuclei. Both overexpression and knockdown of NuSAP impaired cell proliferation. These results suggest a crucial role for NuSAP in spindle microtubule organization. |
format | Text |
id | pubmed-2172854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21728542008-05-01 NuSAP, a novel microtubule-associated protein involved in mitotic spindle organization Raemaekers, Tim Ribbeck, Katharina Beaudouin, Joël Annaert, Wim Van Camp, Mark Stockmans, Ingrid Smets, Nico Bouillon, Roger Ellenberg, Jan Carmeliet, Geert J Cell Biol Article Here, we report on the identification of nucleolar spindle–associated protein (NuSAP), a novel 55-kD vertebrate protein with selective expression in proliferating cells. Its mRNA and protein levels peak at the transition of G2 to mitosis and abruptly decline after cell division. Microscopic analysis of both fixed and live mammalian cells showed that NuSAP is primarily nucleolar in interphase, and localizes prominently to central spindle microtubules during mitosis. Direct interaction of NuSAP with microtubules was demonstrated in vitro. Overexpression of NuSAP caused profound bundling of cytoplasmic microtubules in interphase cells, and this relied on a COOH-terminal microtubule-binding domain. In contrast, depletion of NuSAP by RNA interference resulted in aberrant mitotic spindles, defective chromosome segregation, and cytokinesis. In addition, many NuSAP-depleted interphase cells had deformed nuclei. Both overexpression and knockdown of NuSAP impaired cell proliferation. These results suggest a crucial role for NuSAP in spindle microtubule organization. The Rockefeller University Press 2003-09-15 /pmc/articles/PMC2172854/ /pubmed/12963707 http://dx.doi.org/10.1083/jcb.200302129 Text en Copyright © 2003, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Raemaekers, Tim Ribbeck, Katharina Beaudouin, Joël Annaert, Wim Van Camp, Mark Stockmans, Ingrid Smets, Nico Bouillon, Roger Ellenberg, Jan Carmeliet, Geert NuSAP, a novel microtubule-associated protein involved in mitotic spindle organization |
title | NuSAP, a novel microtubule-associated protein involved in mitotic spindle organization |
title_full | NuSAP, a novel microtubule-associated protein involved in mitotic spindle organization |
title_fullStr | NuSAP, a novel microtubule-associated protein involved in mitotic spindle organization |
title_full_unstemmed | NuSAP, a novel microtubule-associated protein involved in mitotic spindle organization |
title_short | NuSAP, a novel microtubule-associated protein involved in mitotic spindle organization |
title_sort | nusap, a novel microtubule-associated protein involved in mitotic spindle organization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172854/ https://www.ncbi.nlm.nih.gov/pubmed/12963707 http://dx.doi.org/10.1083/jcb.200302129 |
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