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Tension-dependent nucleosome remodeling at the pericentromere in yeast

Nucleosome positioning is important for the structural integrity of chromosomes. During metaphase the mitotic spindle exerts physical force on pericentromeric chromatin. The cell must adjust the pericentromeric chromatin to accommodate the changing tension resulting from microtubule dynamics to main...

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Autores principales: Verdaasdonk, Jolien S., Gardner, Ryan, Stephens, Andrew D., Yeh, Elaine, Bloom, Kerry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3386219/
https://www.ncbi.nlm.nih.gov/pubmed/22593210
http://dx.doi.org/10.1091/mbc.E11-07-0651
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author Verdaasdonk, Jolien S.
Gardner, Ryan
Stephens, Andrew D.
Yeh, Elaine
Bloom, Kerry
author_facet Verdaasdonk, Jolien S.
Gardner, Ryan
Stephens, Andrew D.
Yeh, Elaine
Bloom, Kerry
author_sort Verdaasdonk, Jolien S.
collection PubMed
description Nucleosome positioning is important for the structural integrity of chromosomes. During metaphase the mitotic spindle exerts physical force on pericentromeric chromatin. The cell must adjust the pericentromeric chromatin to accommodate the changing tension resulting from microtubule dynamics to maintain a stable metaphase spindle. Here we examine the effects of spindle-based tension on nucleosome dynamics by measuring the histone turnover of the chromosome arm and the pericentromere during metaphase in the budding yeast Saccharomyces cerevisiae. We find that both histones H2B and H4 exhibit greater turnover in the pericentromere during metaphase. Loss of spindle-based tension by treatment with the microtubule-depolymerizing drug nocodazole or compromising kinetochore function results in reduced histone turnover in the pericentromere. Pericentromeric histone dynamics are influenced by the chromatin-remodeling activities of STH1/NPS1 and ISW2. Sth1p is the ATPase component of the Remodels the Structure of Chromatin (RSC) complex, and Isw2p is an ATP-dependent DNA translocase member of the Imitation Switch (ISWI) subfamily of chromatin-remodeling factors. The balance between displacement and insertion of pericentromeric histones provides a mechanism to accommodate spindle-based tension while maintaining proper chromatin packaging during mitosis.
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spelling pubmed-33862192012-09-16 Tension-dependent nucleosome remodeling at the pericentromere in yeast Verdaasdonk, Jolien S. Gardner, Ryan Stephens, Andrew D. Yeh, Elaine Bloom, Kerry Mol Biol Cell Articles Nucleosome positioning is important for the structural integrity of chromosomes. During metaphase the mitotic spindle exerts physical force on pericentromeric chromatin. The cell must adjust the pericentromeric chromatin to accommodate the changing tension resulting from microtubule dynamics to maintain a stable metaphase spindle. Here we examine the effects of spindle-based tension on nucleosome dynamics by measuring the histone turnover of the chromosome arm and the pericentromere during metaphase in the budding yeast Saccharomyces cerevisiae. We find that both histones H2B and H4 exhibit greater turnover in the pericentromere during metaphase. Loss of spindle-based tension by treatment with the microtubule-depolymerizing drug nocodazole or compromising kinetochore function results in reduced histone turnover in the pericentromere. Pericentromeric histone dynamics are influenced by the chromatin-remodeling activities of STH1/NPS1 and ISW2. Sth1p is the ATPase component of the Remodels the Structure of Chromatin (RSC) complex, and Isw2p is an ATP-dependent DNA translocase member of the Imitation Switch (ISWI) subfamily of chromatin-remodeling factors. The balance between displacement and insertion of pericentromeric histones provides a mechanism to accommodate spindle-based tension while maintaining proper chromatin packaging during mitosis. The American Society for Cell Biology 2012-07-01 /pmc/articles/PMC3386219/ /pubmed/22593210 http://dx.doi.org/10.1091/mbc.E11-07-0651 Text en © 2012 Verdaasdonk et al. 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 (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell BD; are registered trademarks of The American Society of Cell Biology.
spellingShingle Articles
Verdaasdonk, Jolien S.
Gardner, Ryan
Stephens, Andrew D.
Yeh, Elaine
Bloom, Kerry
Tension-dependent nucleosome remodeling at the pericentromere in yeast
title Tension-dependent nucleosome remodeling at the pericentromere in yeast
title_full Tension-dependent nucleosome remodeling at the pericentromere in yeast
title_fullStr Tension-dependent nucleosome remodeling at the pericentromere in yeast
title_full_unstemmed Tension-dependent nucleosome remodeling at the pericentromere in yeast
title_short Tension-dependent nucleosome remodeling at the pericentromere in yeast
title_sort tension-dependent nucleosome remodeling at the pericentromere in yeast
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3386219/
https://www.ncbi.nlm.nih.gov/pubmed/22593210
http://dx.doi.org/10.1091/mbc.E11-07-0651
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