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Quantitative analysis of an anaphase B switch: predicted role for a microtubule catastrophe gradient
Anaphase B in Drosophila embryos is initiated by the inhibition of microtubule (MT) depolymerization at spindle poles, which allows outwardly sliding interpolar (ip) MTs to drive pole–pole separation. Using fluorescence recovery after photobleaching, we observed that MTs throughout the preanaphase B...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064360/ https://www.ncbi.nlm.nih.gov/pubmed/17576796 http://dx.doi.org/10.1083/jcb.200611113 |
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author | Cheerambathur, Dhanya K. Civelekoglu-Scholey, Gul Brust-Mascher, Ingrid Sommi, Patrizia Mogilner, Alex Scholey, Jonathan M. |
author_facet | Cheerambathur, Dhanya K. Civelekoglu-Scholey, Gul Brust-Mascher, Ingrid Sommi, Patrizia Mogilner, Alex Scholey, Jonathan M. |
author_sort | Cheerambathur, Dhanya K. |
collection | PubMed |
description | Anaphase B in Drosophila embryos is initiated by the inhibition of microtubule (MT) depolymerization at spindle poles, which allows outwardly sliding interpolar (ip) MTs to drive pole–pole separation. Using fluorescence recovery after photobleaching, we observed that MTs throughout the preanaphase B spindle are very dynamic and display complete recovery of fluorescence, but during anaphase B, MTs proximal to the poles stabilize and therefore display lower recovery than those elsewhere. Fluorescence microscopy of the MT tip tracker EB1 revealed that growing MT plus ends localize throughout the preanaphase B spindle but concentrate in the overlap region of interpolar MTs (ipMTs) at anaphase B onset. None of these changes occurred in the presence of nondegradable cyclin B. Modeling suggests that they depend on the establishment of a spatial gradient of MT plus-end catastrophe frequencies, decreasing toward the equator. The resulting redistribution of ipMT plus ends to the overlap zone, together with the suppression of minus-end depolymerization at the poles, could constitute a mechanical switch that initiates spindle elongation. |
format | Text |
id | pubmed-2064360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-20643602007-12-18 Quantitative analysis of an anaphase B switch: predicted role for a microtubule catastrophe gradient Cheerambathur, Dhanya K. Civelekoglu-Scholey, Gul Brust-Mascher, Ingrid Sommi, Patrizia Mogilner, Alex Scholey, Jonathan M. J Cell Biol Research Articles Anaphase B in Drosophila embryos is initiated by the inhibition of microtubule (MT) depolymerization at spindle poles, which allows outwardly sliding interpolar (ip) MTs to drive pole–pole separation. Using fluorescence recovery after photobleaching, we observed that MTs throughout the preanaphase B spindle are very dynamic and display complete recovery of fluorescence, but during anaphase B, MTs proximal to the poles stabilize and therefore display lower recovery than those elsewhere. Fluorescence microscopy of the MT tip tracker EB1 revealed that growing MT plus ends localize throughout the preanaphase B spindle but concentrate in the overlap region of interpolar MTs (ipMTs) at anaphase B onset. None of these changes occurred in the presence of nondegradable cyclin B. Modeling suggests that they depend on the establishment of a spatial gradient of MT plus-end catastrophe frequencies, decreasing toward the equator. The resulting redistribution of ipMT plus ends to the overlap zone, together with the suppression of minus-end depolymerization at the poles, could constitute a mechanical switch that initiates spindle elongation. The Rockefeller University Press 2007-06-18 /pmc/articles/PMC2064360/ /pubmed/17576796 http://dx.doi.org/10.1083/jcb.200611113 Text en Copyright © 2007, 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 | Research Articles Cheerambathur, Dhanya K. Civelekoglu-Scholey, Gul Brust-Mascher, Ingrid Sommi, Patrizia Mogilner, Alex Scholey, Jonathan M. Quantitative analysis of an anaphase B switch: predicted role for a microtubule catastrophe gradient |
title | Quantitative analysis of an anaphase B switch: predicted role for a microtubule catastrophe gradient |
title_full | Quantitative analysis of an anaphase B switch: predicted role for a microtubule catastrophe gradient |
title_fullStr | Quantitative analysis of an anaphase B switch: predicted role for a microtubule catastrophe gradient |
title_full_unstemmed | Quantitative analysis of an anaphase B switch: predicted role for a microtubule catastrophe gradient |
title_short | Quantitative analysis of an anaphase B switch: predicted role for a microtubule catastrophe gradient |
title_sort | quantitative analysis of an anaphase b switch: predicted role for a microtubule catastrophe gradient |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064360/ https://www.ncbi.nlm.nih.gov/pubmed/17576796 http://dx.doi.org/10.1083/jcb.200611113 |
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