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Sim4: a novel fission yeast kinetochore protein required for centromeric silencing and chromosome segregation
Fission yeast centromeres are composed of two domains: the central core and the outer repeats. Although both regions are required for full centromere function, the central core has a distinct chromatin structure and is likely to underlie the kinetochore itself, as it is associated with centromere-sp...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172903/ https://www.ncbi.nlm.nih.gov/pubmed/12719471 http://dx.doi.org/10.1083/jcb.200212110 |
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author | Pidoux, Alison L. Richardson, William Allshire, Robin C. |
author_facet | Pidoux, Alison L. Richardson, William Allshire, Robin C. |
author_sort | Pidoux, Alison L. |
collection | PubMed |
description | Fission yeast centromeres are composed of two domains: the central core and the outer repeats. Although both regions are required for full centromere function, the central core has a distinct chromatin structure and is likely to underlie the kinetochore itself, as it is associated with centromere-specific proteins. Genes placed within either region are transcriptionally silenced, reflecting the formation of a functional kinetochore complex and flanking centromeric heterochromatin. Here, transcriptional silencing was exploited to identify components involved in central core silencing and kinetochore assembly or structure. The resulting sim (silencing in the middle of the centromere) mutants display severe chromosome segregation defects. sim2 (+) encodes a known kinetochore protein, the centromere-specific histone H3 variant Cnp1(CENP-A). sim4 (+) encodes a novel essential coiled-coil protein, which is specifically associated with the central core region and is required for the unusual chromatin structure of this region. Sim4 coimmunoprecipitates with the central core component Mis6 and, like Mis6, affects Cnp1(CENP-A) association with the central domain. Functional Mis6 is required for Sim4 localization at the kinetochore. Our analyses illustrate the fundamental link between silencing, chromatin structure, and kinetochore function, and establish defective silencing as a powerful approach for identifying proteins required to build a functional kinetochore. |
format | Text |
id | pubmed-2172903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21729032008-05-01 Sim4: a novel fission yeast kinetochore protein required for centromeric silencing and chromosome segregation Pidoux, Alison L. Richardson, William Allshire, Robin C. J Cell Biol Article Fission yeast centromeres are composed of two domains: the central core and the outer repeats. Although both regions are required for full centromere function, the central core has a distinct chromatin structure and is likely to underlie the kinetochore itself, as it is associated with centromere-specific proteins. Genes placed within either region are transcriptionally silenced, reflecting the formation of a functional kinetochore complex and flanking centromeric heterochromatin. Here, transcriptional silencing was exploited to identify components involved in central core silencing and kinetochore assembly or structure. The resulting sim (silencing in the middle of the centromere) mutants display severe chromosome segregation defects. sim2 (+) encodes a known kinetochore protein, the centromere-specific histone H3 variant Cnp1(CENP-A). sim4 (+) encodes a novel essential coiled-coil protein, which is specifically associated with the central core region and is required for the unusual chromatin structure of this region. Sim4 coimmunoprecipitates with the central core component Mis6 and, like Mis6, affects Cnp1(CENP-A) association with the central domain. Functional Mis6 is required for Sim4 localization at the kinetochore. Our analyses illustrate the fundamental link between silencing, chromatin structure, and kinetochore function, and establish defective silencing as a powerful approach for identifying proteins required to build a functional kinetochore. The Rockefeller University Press 2003-04-28 /pmc/articles/PMC2172903/ /pubmed/12719471 http://dx.doi.org/10.1083/jcb.200212110 Text en Copyright © 2003, The Rockefeller University Press 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 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Pidoux, Alison L. Richardson, William Allshire, Robin C. Sim4: a novel fission yeast kinetochore protein required for centromeric silencing and chromosome segregation |
title | Sim4: a novel fission yeast kinetochore protein required for centromeric silencing and chromosome segregation |
title_full | Sim4: a novel fission yeast kinetochore protein required for centromeric silencing and chromosome segregation |
title_fullStr | Sim4: a novel fission yeast kinetochore protein required for centromeric silencing and chromosome segregation |
title_full_unstemmed | Sim4: a novel fission yeast kinetochore protein required for centromeric silencing and chromosome segregation |
title_short | Sim4: a novel fission yeast kinetochore protein required for centromeric silencing and chromosome segregation |
title_sort | sim4: a novel fission yeast kinetochore protein required for centromeric silencing and chromosome segregation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172903/ https://www.ncbi.nlm.nih.gov/pubmed/12719471 http://dx.doi.org/10.1083/jcb.200212110 |
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