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CENP-A Regulation and Cancer
In mammals, CENP-A, a histone H3 variant found in the centromeric chromatin, is critical for faithful chromosome segregation and genome integrity maintenance through cell divisions. Specifically, it has dual functions, enabling to define epigenetically the centromere position and providing the found...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201071/ https://www.ncbi.nlm.nih.gov/pubmed/35721491 http://dx.doi.org/10.3389/fcell.2022.907120 |
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author | Renaud-Pageot, Charlène Quivy, Jean-Pierre Lochhead, Marina Almouzni, Geneviève |
author_facet | Renaud-Pageot, Charlène Quivy, Jean-Pierre Lochhead, Marina Almouzni, Geneviève |
author_sort | Renaud-Pageot, Charlène |
collection | PubMed |
description | In mammals, CENP-A, a histone H3 variant found in the centromeric chromatin, is critical for faithful chromosome segregation and genome integrity maintenance through cell divisions. Specifically, it has dual functions, enabling to define epigenetically the centromere position and providing the foundation for building up the kinetochore. Regulation of its dynamics of synthesis and deposition ensures to propagate proper centromeres on each chromosome across mitosis and meiosis. However, CENP-A overexpression is a feature identified in many cancers. Importantly, high levels of CENP-A lead to its mislocalization outside the centromere. Recent studies in mammals have begun to uncover how CENP-A overexpression can affect genome integrity, reprogram cell fate and impact 3D nuclear organization in cancer. Here, we summarize the mechanisms that orchestrate CENP-A regulation. Then we review how, beyond its centromeric function, CENP-A overexpression is linked to cancer state in mammalian cells, with a focus on the perturbations that ensue at the level of chromatin organization. Finally, we review the clinical interest for CENP-A in cancer treatment. |
format | Online Article Text |
id | pubmed-9201071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92010712022-06-17 CENP-A Regulation and Cancer Renaud-Pageot, Charlène Quivy, Jean-Pierre Lochhead, Marina Almouzni, Geneviève Front Cell Dev Biol Cell and Developmental Biology In mammals, CENP-A, a histone H3 variant found in the centromeric chromatin, is critical for faithful chromosome segregation and genome integrity maintenance through cell divisions. Specifically, it has dual functions, enabling to define epigenetically the centromere position and providing the foundation for building up the kinetochore. Regulation of its dynamics of synthesis and deposition ensures to propagate proper centromeres on each chromosome across mitosis and meiosis. However, CENP-A overexpression is a feature identified in many cancers. Importantly, high levels of CENP-A lead to its mislocalization outside the centromere. Recent studies in mammals have begun to uncover how CENP-A overexpression can affect genome integrity, reprogram cell fate and impact 3D nuclear organization in cancer. Here, we summarize the mechanisms that orchestrate CENP-A regulation. Then we review how, beyond its centromeric function, CENP-A overexpression is linked to cancer state in mammalian cells, with a focus on the perturbations that ensue at the level of chromatin organization. Finally, we review the clinical interest for CENP-A in cancer treatment. Frontiers Media S.A. 2022-06-02 /pmc/articles/PMC9201071/ /pubmed/35721491 http://dx.doi.org/10.3389/fcell.2022.907120 Text en Copyright © 2022 Renaud-Pageot, Quivy, Lochhead and Almouzni. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Renaud-Pageot, Charlène Quivy, Jean-Pierre Lochhead, Marina Almouzni, Geneviève CENP-A Regulation and Cancer |
title | CENP-A Regulation and Cancer |
title_full | CENP-A Regulation and Cancer |
title_fullStr | CENP-A Regulation and Cancer |
title_full_unstemmed | CENP-A Regulation and Cancer |
title_short | CENP-A Regulation and Cancer |
title_sort | cenp-a regulation and cancer |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201071/ https://www.ncbi.nlm.nih.gov/pubmed/35721491 http://dx.doi.org/10.3389/fcell.2022.907120 |
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