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A dynamical model of the spindle position checkpoint
The orientation of the mitotic spindle with respect to the polarity axis is crucial for the accuracy of asymmetric cell division. In budding yeast, a surveillance mechanism called the spindle position checkpoint (SPOC) prevents exit from mitosis when the mitotic spindle fails to align along the moth...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Molecular Biology Organization
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377990/ https://www.ncbi.nlm.nih.gov/pubmed/22580890 http://dx.doi.org/10.1038/msb.2012.15 |
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author | Caydasi, Ayse Koca Lohel, Maiko Grünert, Gerd Dittrich, Peter Pereira, Gislene Ibrahim, Bashar |
author_facet | Caydasi, Ayse Koca Lohel, Maiko Grünert, Gerd Dittrich, Peter Pereira, Gislene Ibrahim, Bashar |
author_sort | Caydasi, Ayse Koca |
collection | PubMed |
description | The orientation of the mitotic spindle with respect to the polarity axis is crucial for the accuracy of asymmetric cell division. In budding yeast, a surveillance mechanism called the spindle position checkpoint (SPOC) prevents exit from mitosis when the mitotic spindle fails to align along the mother-to-daughter polarity axis. SPOC arrest relies upon inhibition of the GTPase Tem1 by the GTPase-activating protein (GAP) complex Bfa1–Bub2. Importantly, reactions signaling mitotic exit take place at yeast centrosomes (named spindle pole bodies, SPBs) and the GAP complex also promotes SPB localization of Tem1. Yet, whether the regulation of Tem1 by Bfa1–Bub2 takes place only at the SPBs remains elusive. Here, we present a quantitative analysis of Bfa1–Bub2 and Tem1 localization at the SPBs. Based on the measured SPB-bound protein levels, we introduce a dynamical model of the SPOC that describes the regulation of Bfa1 and Tem1. Our model suggests that Bfa1 interacts with Tem1 in the cytoplasm as well as at the SPBs to provide efficient Tem1 inhibition. |
format | Online Article Text |
id | pubmed-3377990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | European Molecular Biology Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-33779902012-06-20 A dynamical model of the spindle position checkpoint Caydasi, Ayse Koca Lohel, Maiko Grünert, Gerd Dittrich, Peter Pereira, Gislene Ibrahim, Bashar Mol Syst Biol Article The orientation of the mitotic spindle with respect to the polarity axis is crucial for the accuracy of asymmetric cell division. In budding yeast, a surveillance mechanism called the spindle position checkpoint (SPOC) prevents exit from mitosis when the mitotic spindle fails to align along the mother-to-daughter polarity axis. SPOC arrest relies upon inhibition of the GTPase Tem1 by the GTPase-activating protein (GAP) complex Bfa1–Bub2. Importantly, reactions signaling mitotic exit take place at yeast centrosomes (named spindle pole bodies, SPBs) and the GAP complex also promotes SPB localization of Tem1. Yet, whether the regulation of Tem1 by Bfa1–Bub2 takes place only at the SPBs remains elusive. Here, we present a quantitative analysis of Bfa1–Bub2 and Tem1 localization at the SPBs. Based on the measured SPB-bound protein levels, we introduce a dynamical model of the SPOC that describes the regulation of Bfa1 and Tem1. Our model suggests that Bfa1 interacts with Tem1 in the cytoplasm as well as at the SPBs to provide efficient Tem1 inhibition. European Molecular Biology Organization 2012-05-08 /pmc/articles/PMC3377990/ /pubmed/22580890 http://dx.doi.org/10.1038/msb.2012.15 Text en Copyright © 2012, EMBO and Macmillan Publishers Limited https://creativecommons.org/licenses/by-nc-nd/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial No Derivative Works 3.0 Unported License, which permits distribution and reproduction in any medium, provided the original author and source are credited. This license does not permit commercial exploitation or the creation of derivative works without specific permission. |
spellingShingle | Article Caydasi, Ayse Koca Lohel, Maiko Grünert, Gerd Dittrich, Peter Pereira, Gislene Ibrahim, Bashar A dynamical model of the spindle position checkpoint |
title | A dynamical model of the spindle position checkpoint |
title_full | A dynamical model of the spindle position checkpoint |
title_fullStr | A dynamical model of the spindle position checkpoint |
title_full_unstemmed | A dynamical model of the spindle position checkpoint |
title_short | A dynamical model of the spindle position checkpoint |
title_sort | dynamical model of the spindle position checkpoint |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377990/ https://www.ncbi.nlm.nih.gov/pubmed/22580890 http://dx.doi.org/10.1038/msb.2012.15 |
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