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The quantitative architecture of centromeric chromatin
The centromere, responsible for chromosome segregation during mitosis, is epigenetically defined by CENP-A containing chromatin. The amount of centromeric CENP-A has direct implications for both the architecture and epigenetic inheritance of centromeres. Using complementary strategies, we determined...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091408/ https://www.ncbi.nlm.nih.gov/pubmed/25027692 http://dx.doi.org/10.7554/eLife.02137 |
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author | Bodor, Dani L Mata, João F Sergeev, Mikhail David, Ana Filipa Salimian, Kevan J Panchenko, Tanya Cleveland, Don W Black, Ben E Shah, Jagesh V Jansen, Lars ET |
author_facet | Bodor, Dani L Mata, João F Sergeev, Mikhail David, Ana Filipa Salimian, Kevan J Panchenko, Tanya Cleveland, Don W Black, Ben E Shah, Jagesh V Jansen, Lars ET |
author_sort | Bodor, Dani L |
collection | PubMed |
description | The centromere, responsible for chromosome segregation during mitosis, is epigenetically defined by CENP-A containing chromatin. The amount of centromeric CENP-A has direct implications for both the architecture and epigenetic inheritance of centromeres. Using complementary strategies, we determined that typical human centromeres contain ∼400 molecules of CENP-A, which is controlled by a mass-action mechanism. This number, despite representing only ∼4% of all centromeric nucleosomes, forms a ∼50-fold enrichment to the overall genome. In addition, although pre-assembled CENP-A is randomly segregated during cell division, this amount of CENP-A is sufficient to prevent stochastic loss of centromere function and identity. Finally, we produced a statistical map of CENP-A occupancy at a human neocentromere and identified nucleosome positions that feature CENP-A in a majority of cells. In summary, we present a quantitative view of the centromere that provides a mechanistic framework for both robust epigenetic inheritance of centromeres and the paucity of neocentromere formation. DOI: http://dx.doi.org/10.7554/eLife.02137.001 |
format | Online Article Text |
id | pubmed-4091408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-40914082014-07-22 The quantitative architecture of centromeric chromatin Bodor, Dani L Mata, João F Sergeev, Mikhail David, Ana Filipa Salimian, Kevan J Panchenko, Tanya Cleveland, Don W Black, Ben E Shah, Jagesh V Jansen, Lars ET eLife Cell Biology The centromere, responsible for chromosome segregation during mitosis, is epigenetically defined by CENP-A containing chromatin. The amount of centromeric CENP-A has direct implications for both the architecture and epigenetic inheritance of centromeres. Using complementary strategies, we determined that typical human centromeres contain ∼400 molecules of CENP-A, which is controlled by a mass-action mechanism. This number, despite representing only ∼4% of all centromeric nucleosomes, forms a ∼50-fold enrichment to the overall genome. In addition, although pre-assembled CENP-A is randomly segregated during cell division, this amount of CENP-A is sufficient to prevent stochastic loss of centromere function and identity. Finally, we produced a statistical map of CENP-A occupancy at a human neocentromere and identified nucleosome positions that feature CENP-A in a majority of cells. In summary, we present a quantitative view of the centromere that provides a mechanistic framework for both robust epigenetic inheritance of centromeres and the paucity of neocentromere formation. DOI: http://dx.doi.org/10.7554/eLife.02137.001 eLife Sciences Publications, Ltd 2014-07-15 /pmc/articles/PMC4091408/ /pubmed/25027692 http://dx.doi.org/10.7554/eLife.02137 Text en Copyright © 2014, Bodor et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Bodor, Dani L Mata, João F Sergeev, Mikhail David, Ana Filipa Salimian, Kevan J Panchenko, Tanya Cleveland, Don W Black, Ben E Shah, Jagesh V Jansen, Lars ET The quantitative architecture of centromeric chromatin |
title | The quantitative architecture of centromeric chromatin |
title_full | The quantitative architecture of centromeric chromatin |
title_fullStr | The quantitative architecture of centromeric chromatin |
title_full_unstemmed | The quantitative architecture of centromeric chromatin |
title_short | The quantitative architecture of centromeric chromatin |
title_sort | quantitative architecture of centromeric chromatin |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091408/ https://www.ncbi.nlm.nih.gov/pubmed/25027692 http://dx.doi.org/10.7554/eLife.02137 |
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