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Chromosome misalignment is associated with PLK1 activity at cenexin-positive mitotic centrosomes
The mitotic kinase, polo-like kinase 1 (PLK1), facilitates the assembly of the two mitotic spindle poles, which are required for the formation of the microtubule-based spindle that ensures appropriate chromosome distribution into the two forming daughter cells. Spindle poles are asymmetric in compos...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6727634/ https://www.ncbi.nlm.nih.gov/pubmed/31042116 http://dx.doi.org/10.1091/mbc.E18-12-0817 |
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author | Colicino, Erica G. Stevens, Katrina Curtis, Erin Rathbun, Lindsay Bates, Michael Manikas, Julie Amack, Jeffrey Freshour, Judy Hehnly, Heidi |
author_facet | Colicino, Erica G. Stevens, Katrina Curtis, Erin Rathbun, Lindsay Bates, Michael Manikas, Julie Amack, Jeffrey Freshour, Judy Hehnly, Heidi |
author_sort | Colicino, Erica G. |
collection | PubMed |
description | The mitotic kinase, polo-like kinase 1 (PLK1), facilitates the assembly of the two mitotic spindle poles, which are required for the formation of the microtubule-based spindle that ensures appropriate chromosome distribution into the two forming daughter cells. Spindle poles are asymmetric in composition. One spindle pole contains the oldest mitotic centriole, the mother centriole, where the majority of cenexin, the mother centriole appendage protein and PLK1 binding partner, resides. We hypothesized that PLK1 activity is greater at the cenexin-positive older spindle pole. Our studies found that PLK1 asymmetrically localizes between spindle poles under conditions of chromosome misalignment, and chromosomes tend to misalign toward the oldest spindle pole in a cenexin- and PLK1-dependent manner. During chromosome misalignment, PLK1 activity is increased specifically at the oldest spindle pole, and this increase in activity is lost in cenexin-depleted cells. We propose a model where PLK1 activity elevates in response to misaligned chromosomes at the oldest spindle pole during metaphase. |
format | Online Article Text |
id | pubmed-6727634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-67276342019-09-08 Chromosome misalignment is associated with PLK1 activity at cenexin-positive mitotic centrosomes Colicino, Erica G. Stevens, Katrina Curtis, Erin Rathbun, Lindsay Bates, Michael Manikas, Julie Amack, Jeffrey Freshour, Judy Hehnly, Heidi Mol Biol Cell Articles The mitotic kinase, polo-like kinase 1 (PLK1), facilitates the assembly of the two mitotic spindle poles, which are required for the formation of the microtubule-based spindle that ensures appropriate chromosome distribution into the two forming daughter cells. Spindle poles are asymmetric in composition. One spindle pole contains the oldest mitotic centriole, the mother centriole, where the majority of cenexin, the mother centriole appendage protein and PLK1 binding partner, resides. We hypothesized that PLK1 activity is greater at the cenexin-positive older spindle pole. Our studies found that PLK1 asymmetrically localizes between spindle poles under conditions of chromosome misalignment, and chromosomes tend to misalign toward the oldest spindle pole in a cenexin- and PLK1-dependent manner. During chromosome misalignment, PLK1 activity is increased specifically at the oldest spindle pole, and this increase in activity is lost in cenexin-depleted cells. We propose a model where PLK1 activity elevates in response to misaligned chromosomes at the oldest spindle pole during metaphase. The American Society for Cell Biology 2019-06-15 /pmc/articles/PMC6727634/ /pubmed/31042116 http://dx.doi.org/10.1091/mbc.E18-12-0817 Text en © 2019 Colicino 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. http://creativecommons.org/licenses/by-nc-sa/3.0 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 3.0 Unported Creative Commons License. |
spellingShingle | Articles Colicino, Erica G. Stevens, Katrina Curtis, Erin Rathbun, Lindsay Bates, Michael Manikas, Julie Amack, Jeffrey Freshour, Judy Hehnly, Heidi Chromosome misalignment is associated with PLK1 activity at cenexin-positive mitotic centrosomes |
title | Chromosome misalignment is associated with PLK1 activity at cenexin-positive mitotic centrosomes |
title_full | Chromosome misalignment is associated with PLK1 activity at cenexin-positive mitotic centrosomes |
title_fullStr | Chromosome misalignment is associated with PLK1 activity at cenexin-positive mitotic centrosomes |
title_full_unstemmed | Chromosome misalignment is associated with PLK1 activity at cenexin-positive mitotic centrosomes |
title_short | Chromosome misalignment is associated with PLK1 activity at cenexin-positive mitotic centrosomes |
title_sort | chromosome misalignment is associated with plk1 activity at cenexin-positive mitotic centrosomes |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6727634/ https://www.ncbi.nlm.nih.gov/pubmed/31042116 http://dx.doi.org/10.1091/mbc.E18-12-0817 |
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