Cargando…
A computational model predicts Xenopus meiotic spindle organization
The metaphase spindle is a dynamic bipolar structure crucial for proper chromosome segregation, but how microtubules (MTs) are organized within the bipolar architecture remains controversial. To explore MT organization along the pole-to-pole axis, we simulated meiotic spindle assembly in two dimensi...
Autores principales: | , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3010074/ https://www.ncbi.nlm.nih.gov/pubmed/21173114 http://dx.doi.org/10.1083/jcb.201006076 |
_version_ | 1782194773727117312 |
---|---|
author | Loughlin, Rose Heald, Rebecca Nédélec, François |
author_facet | Loughlin, Rose Heald, Rebecca Nédélec, François |
author_sort | Loughlin, Rose |
collection | PubMed |
description | The metaphase spindle is a dynamic bipolar structure crucial for proper chromosome segregation, but how microtubules (MTs) are organized within the bipolar architecture remains controversial. To explore MT organization along the pole-to-pole axis, we simulated meiotic spindle assembly in two dimensions using dynamic MTs, a MT cross-linking force, and a kinesin-5–like motor. The bipolar structures that form consist of antiparallel fluxing MTs, but spindle pole formation requires the addition of a NuMA-like minus-end cross-linker and directed transport of MT depolymerization activity toward minus ends. Dynamic instability and minus-end depolymerization generate realistic MT lifetimes and a truncated exponential MT length distribution. Keeping the number of MTs in the simulation constant, we explored the influence of two different MT nucleation pathways on spindle organization. When nucleation occurs throughout the spindle, the simulation quantitatively reproduces features of meiotic spindles assembled in Xenopus egg extracts. |
format | Text |
id | pubmed-3010074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-30100742011-06-27 A computational model predicts Xenopus meiotic spindle organization Loughlin, Rose Heald, Rebecca Nédélec, François J Cell Biol Research Articles The metaphase spindle is a dynamic bipolar structure crucial for proper chromosome segregation, but how microtubules (MTs) are organized within the bipolar architecture remains controversial. To explore MT organization along the pole-to-pole axis, we simulated meiotic spindle assembly in two dimensions using dynamic MTs, a MT cross-linking force, and a kinesin-5–like motor. The bipolar structures that form consist of antiparallel fluxing MTs, but spindle pole formation requires the addition of a NuMA-like minus-end cross-linker and directed transport of MT depolymerization activity toward minus ends. Dynamic instability and minus-end depolymerization generate realistic MT lifetimes and a truncated exponential MT length distribution. Keeping the number of MTs in the simulation constant, we explored the influence of two different MT nucleation pathways on spindle organization. When nucleation occurs throughout the spindle, the simulation quantitatively reproduces features of meiotic spindles assembled in Xenopus egg extracts. The Rockefeller University Press 2010-12-27 /pmc/articles/PMC3010074/ /pubmed/21173114 http://dx.doi.org/10.1083/jcb.201006076 Text en © 2010 Loughlin et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Loughlin, Rose Heald, Rebecca Nédélec, François A computational model predicts Xenopus meiotic spindle organization |
title | A computational model predicts Xenopus meiotic spindle organization |
title_full | A computational model predicts Xenopus meiotic spindle organization |
title_fullStr | A computational model predicts Xenopus meiotic spindle organization |
title_full_unstemmed | A computational model predicts Xenopus meiotic spindle organization |
title_short | A computational model predicts Xenopus meiotic spindle organization |
title_sort | computational model predicts xenopus meiotic spindle organization |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3010074/ https://www.ncbi.nlm.nih.gov/pubmed/21173114 http://dx.doi.org/10.1083/jcb.201006076 |
work_keys_str_mv | AT loughlinrose acomputationalmodelpredictsxenopusmeioticspindleorganization AT healdrebecca acomputationalmodelpredictsxenopusmeioticspindleorganization AT nedelecfrancois acomputationalmodelpredictsxenopusmeioticspindleorganization AT loughlinrose computationalmodelpredictsxenopusmeioticspindleorganization AT healdrebecca computationalmodelpredictsxenopusmeioticspindleorganization AT nedelecfrancois computationalmodelpredictsxenopusmeioticspindleorganization |