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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...

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Autores principales: Raemaekers, Tim, Ribbeck, Katharina, Beaudouin, Joël, Annaert, Wim, Van Camp, Mark, Stockmans, Ingrid, Smets, Nico, Bouillon, Roger, Ellenberg, Jan, Carmeliet, Geert
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2003
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.
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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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