Cargando…
Microtubule competition and cell growth recenter the nucleus after anaphase in fission yeast
Cells actively position their nuclei based on their activity. In fission yeast, microtubule-dependent nuclear centering is critical for symmetrical cell division. After spindle disassembly at the end of anaphase, the nucleus recenters over an ∼90-min period, approximately half of the duration of the...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10398876/ https://www.ncbi.nlm.nih.gov/pubmed/37099380 http://dx.doi.org/10.1091/mbc.E23-01-0034 |
_version_ | 1785084122854588416 |
---|---|
author | Bellingham-Johnstun, Kimberly Thorn, Annelise Belmonte, Julio M. Laplante, Caroline |
author_facet | Bellingham-Johnstun, Kimberly Thorn, Annelise Belmonte, Julio M. Laplante, Caroline |
author_sort | Bellingham-Johnstun, Kimberly |
collection | PubMed |
description | Cells actively position their nuclei based on their activity. In fission yeast, microtubule-dependent nuclear centering is critical for symmetrical cell division. After spindle disassembly at the end of anaphase, the nucleus recenters over an ∼90-min period, approximately half of the duration of the cell cycle. Live-cell and simulation experiments support the cooperation of two distinct microtubule competition mechanisms in the slow recentering of the nucleus. First, a push–push mechanism acts from spindle disassembly to septation and involves the opposing actions of the mitotic spindle pole body microtubules that push the nucleus away from the ends of the cell, while a postanaphase array of microtubules baskets the nucleus and limits its migration toward the division plane. Second, a slow-and-grow mechanism slowly centers the nucleus in the newborn cell by a combination of microtubule competition and asymmetric cell growth. Our work underlines how intrinsic properties of microtubules differently impact nuclear positioning according to microtubule network organization and cell size. |
format | Online Article Text |
id | pubmed-10398876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-103988762023-09-16 Microtubule competition and cell growth recenter the nucleus after anaphase in fission yeast Bellingham-Johnstun, Kimberly Thorn, Annelise Belmonte, Julio M. Laplante, Caroline Mol Biol Cell Articles Cells actively position their nuclei based on their activity. In fission yeast, microtubule-dependent nuclear centering is critical for symmetrical cell division. After spindle disassembly at the end of anaphase, the nucleus recenters over an ∼90-min period, approximately half of the duration of the cell cycle. Live-cell and simulation experiments support the cooperation of two distinct microtubule competition mechanisms in the slow recentering of the nucleus. First, a push–push mechanism acts from spindle disassembly to septation and involves the opposing actions of the mitotic spindle pole body microtubules that push the nucleus away from the ends of the cell, while a postanaphase array of microtubules baskets the nucleus and limits its migration toward the division plane. Second, a slow-and-grow mechanism slowly centers the nucleus in the newborn cell by a combination of microtubule competition and asymmetric cell growth. Our work underlines how intrinsic properties of microtubules differently impact nuclear positioning according to microtubule network organization and cell size. The American Society for Cell Biology 2023-07-01 /pmc/articles/PMC10398876/ /pubmed/37099380 http://dx.doi.org/10.1091/mbc.E23-01-0034 Text en © 2023 Bellingham-Johnstun et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial-Share Alike 4.0 International Creative Commons License. |
spellingShingle | Articles Bellingham-Johnstun, Kimberly Thorn, Annelise Belmonte, Julio M. Laplante, Caroline Microtubule competition and cell growth recenter the nucleus after anaphase in fission yeast |
title | Microtubule competition and cell growth recenter the nucleus after anaphase in fission yeast |
title_full | Microtubule competition and cell growth recenter the nucleus after anaphase in fission yeast |
title_fullStr | Microtubule competition and cell growth recenter the nucleus after anaphase in fission yeast |
title_full_unstemmed | Microtubule competition and cell growth recenter the nucleus after anaphase in fission yeast |
title_short | Microtubule competition and cell growth recenter the nucleus after anaphase in fission yeast |
title_sort | microtubule competition and cell growth recenter the nucleus after anaphase in fission yeast |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10398876/ https://www.ncbi.nlm.nih.gov/pubmed/37099380 http://dx.doi.org/10.1091/mbc.E23-01-0034 |
work_keys_str_mv | AT bellinghamjohnstunkimberly microtubulecompetitionandcellgrowthrecenterthenucleusafteranaphaseinfissionyeast AT thornannelise microtubulecompetitionandcellgrowthrecenterthenucleusafteranaphaseinfissionyeast AT belmontejuliom microtubulecompetitionandcellgrowthrecenterthenucleusafteranaphaseinfissionyeast AT laplantecaroline microtubulecompetitionandcellgrowthrecenterthenucleusafteranaphaseinfissionyeast |