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The SWI/SNF complex acts to constrain distribution of the centromeric histone variant Cse4

In order to gain insight into the function of the Saccharomyces cerevisiae SWI/SNF complex, we have identified DNA sequences to which it is bound genomewide. One surprising observation is that the complex is enriched at the centromeres of each chromosome. Deletion of the gene encoding the Snf2 subun...

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Autores principales: Gkikopoulos, Triantaffyllos, Singh, Vijender, Tsui, Kyle, Awad, Salma, Renshaw, Matthew J, Scholfield, Pieta, Barton, Geoffrey J, Nislow, Corey, Tanaka, Tomoyuki U, Owen-Hughes, Tom
Formato: Texto
Lenguaje:English
Publicado: European Molecular Biology Organization 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098484/
https://www.ncbi.nlm.nih.gov/pubmed/21505420
http://dx.doi.org/10.1038/emboj.2011.112
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author Gkikopoulos, Triantaffyllos
Singh, Vijender
Tsui, Kyle
Awad, Salma
Renshaw, Matthew J
Scholfield, Pieta
Barton, Geoffrey J
Nislow, Corey
Tanaka, Tomoyuki U
Owen-Hughes, Tom
author_facet Gkikopoulos, Triantaffyllos
Singh, Vijender
Tsui, Kyle
Awad, Salma
Renshaw, Matthew J
Scholfield, Pieta
Barton, Geoffrey J
Nislow, Corey
Tanaka, Tomoyuki U
Owen-Hughes, Tom
author_sort Gkikopoulos, Triantaffyllos
collection PubMed
description In order to gain insight into the function of the Saccharomyces cerevisiae SWI/SNF complex, we have identified DNA sequences to which it is bound genomewide. One surprising observation is that the complex is enriched at the centromeres of each chromosome. Deletion of the gene encoding the Snf2 subunit of the complex was found to cause partial redistribution of the centromeric histone variant Cse4 to sites on chromosome arms. Cultures of snf2Δ yeast were found to progress through mitosis slowly. This was dependent on the mitotic checkpoint protein Mad2. In the absence of Mad2, defects in chromosome segregation were observed. In the absence of Snf2, chromatin organisation at centromeres is less distinct. In particular, hypersensitive sites flanking the Cse4 containing nucleosomes are less pronounced. Furthermore, SWI/SNF complex was found to be especially effective in the dissociation of Cse4 containing chromatin in vitro. This suggests a role for Snf2 in the maintenance of point centromeres involving the removal of Cse4 from ectopic sites.
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spelling pubmed-30984842011-07-05 The SWI/SNF complex acts to constrain distribution of the centromeric histone variant Cse4 Gkikopoulos, Triantaffyllos Singh, Vijender Tsui, Kyle Awad, Salma Renshaw, Matthew J Scholfield, Pieta Barton, Geoffrey J Nislow, Corey Tanaka, Tomoyuki U Owen-Hughes, Tom EMBO J Article In order to gain insight into the function of the Saccharomyces cerevisiae SWI/SNF complex, we have identified DNA sequences to which it is bound genomewide. One surprising observation is that the complex is enriched at the centromeres of each chromosome. Deletion of the gene encoding the Snf2 subunit of the complex was found to cause partial redistribution of the centromeric histone variant Cse4 to sites on chromosome arms. Cultures of snf2Δ yeast were found to progress through mitosis slowly. This was dependent on the mitotic checkpoint protein Mad2. In the absence of Mad2, defects in chromosome segregation were observed. In the absence of Snf2, chromatin organisation at centromeres is less distinct. In particular, hypersensitive sites flanking the Cse4 containing nucleosomes are less pronounced. Furthermore, SWI/SNF complex was found to be especially effective in the dissociation of Cse4 containing chromatin in vitro. This suggests a role for Snf2 in the maintenance of point centromeres involving the removal of Cse4 from ectopic sites. European Molecular Biology Organization 2011-05-18 2011-04-19 /pmc/articles/PMC3098484/ /pubmed/21505420 http://dx.doi.org/10.1038/emboj.2011.112 Text en Copyright © 2011, European Molecular Biology Organization https://creativecommons.org/licenses/by-nc-nd/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial No Derivative Works 3.0 Unported License, which permits distribution and reproduction in any medium, provided the original author and source are credited. This license does not permit commercial exploitation or the creation of derivative works without specific permission.
spellingShingle Article
Gkikopoulos, Triantaffyllos
Singh, Vijender
Tsui, Kyle
Awad, Salma
Renshaw, Matthew J
Scholfield, Pieta
Barton, Geoffrey J
Nislow, Corey
Tanaka, Tomoyuki U
Owen-Hughes, Tom
The SWI/SNF complex acts to constrain distribution of the centromeric histone variant Cse4
title The SWI/SNF complex acts to constrain distribution of the centromeric histone variant Cse4
title_full The SWI/SNF complex acts to constrain distribution of the centromeric histone variant Cse4
title_fullStr The SWI/SNF complex acts to constrain distribution of the centromeric histone variant Cse4
title_full_unstemmed The SWI/SNF complex acts to constrain distribution of the centromeric histone variant Cse4
title_short The SWI/SNF complex acts to constrain distribution of the centromeric histone variant Cse4
title_sort swi/snf complex acts to constrain distribution of the centromeric histone variant cse4
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098484/
https://www.ncbi.nlm.nih.gov/pubmed/21505420
http://dx.doi.org/10.1038/emboj.2011.112
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