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The localization of centromere protein A is conserved among tissues

Centromeres are epigenetically specified by the histone H3 variant CENP-A. Although mammalian centromeres are typically associated with satellite DNA, we previously demonstrated that the centromere of horse chromosome 11 (ECA11) is completely devoid of satellite DNA. We also showed that the localiza...

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Autores principales: Cappelletti, Eleonora, Piras, Francesca M., Sola, Lorenzo, Santagostino, Marco, Petersen, Jessica L., Bellone, Rebecca R., Finno, Carrie J., Peng, Sichong, Kalbfleisch, Ted S., Bailey, Ernest, Nergadze, Solomon G., Giulotto, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514049/
https://www.ncbi.nlm.nih.gov/pubmed/37735603
http://dx.doi.org/10.1038/s42003-023-05335-7
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author Cappelletti, Eleonora
Piras, Francesca M.
Sola, Lorenzo
Santagostino, Marco
Petersen, Jessica L.
Bellone, Rebecca R.
Finno, Carrie J.
Peng, Sichong
Kalbfleisch, Ted S.
Bailey, Ernest
Nergadze, Solomon G.
Giulotto, Elena
author_facet Cappelletti, Eleonora
Piras, Francesca M.
Sola, Lorenzo
Santagostino, Marco
Petersen, Jessica L.
Bellone, Rebecca R.
Finno, Carrie J.
Peng, Sichong
Kalbfleisch, Ted S.
Bailey, Ernest
Nergadze, Solomon G.
Giulotto, Elena
author_sort Cappelletti, Eleonora
collection PubMed
description Centromeres are epigenetically specified by the histone H3 variant CENP-A. Although mammalian centromeres are typically associated with satellite DNA, we previously demonstrated that the centromere of horse chromosome 11 (ECA11) is completely devoid of satellite DNA. We also showed that the localization of its CENP-A binding domain is not fixed but slides within an about 500 kb region in different individuals, giving rise to positional alleles. These epialleles are inherited as Mendelian traits but their position can move in one generation. It is still unknown whether centromere sliding occurs during meiosis or during development. Here, we first improve the sequence of the ECA11 centromeric region in the EquCab3.0 assembly. Then, to test whether centromere sliding may occur during development, we map the CENP-A binding domains of ECA11 using ChIP-seq in five tissues of different embryonic origin from the four horses of the equine FAANG (Functional Annotation of ANimal Genomes) consortium. Our results demonstrate that the centromere is localized in the same region in all tissues, suggesting that the position of the centromeric domain is maintained during development.
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spelling pubmed-105140492023-09-23 The localization of centromere protein A is conserved among tissues Cappelletti, Eleonora Piras, Francesca M. Sola, Lorenzo Santagostino, Marco Petersen, Jessica L. Bellone, Rebecca R. Finno, Carrie J. Peng, Sichong Kalbfleisch, Ted S. Bailey, Ernest Nergadze, Solomon G. Giulotto, Elena Commun Biol Article Centromeres are epigenetically specified by the histone H3 variant CENP-A. Although mammalian centromeres are typically associated with satellite DNA, we previously demonstrated that the centromere of horse chromosome 11 (ECA11) is completely devoid of satellite DNA. We also showed that the localization of its CENP-A binding domain is not fixed but slides within an about 500 kb region in different individuals, giving rise to positional alleles. These epialleles are inherited as Mendelian traits but their position can move in one generation. It is still unknown whether centromere sliding occurs during meiosis or during development. Here, we first improve the sequence of the ECA11 centromeric region in the EquCab3.0 assembly. Then, to test whether centromere sliding may occur during development, we map the CENP-A binding domains of ECA11 using ChIP-seq in five tissues of different embryonic origin from the four horses of the equine FAANG (Functional Annotation of ANimal Genomes) consortium. Our results demonstrate that the centromere is localized in the same region in all tissues, suggesting that the position of the centromeric domain is maintained during development. Nature Publishing Group UK 2023-09-21 /pmc/articles/PMC10514049/ /pubmed/37735603 http://dx.doi.org/10.1038/s42003-023-05335-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Cappelletti, Eleonora
Piras, Francesca M.
Sola, Lorenzo
Santagostino, Marco
Petersen, Jessica L.
Bellone, Rebecca R.
Finno, Carrie J.
Peng, Sichong
Kalbfleisch, Ted S.
Bailey, Ernest
Nergadze, Solomon G.
Giulotto, Elena
The localization of centromere protein A is conserved among tissues
title The localization of centromere protein A is conserved among tissues
title_full The localization of centromere protein A is conserved among tissues
title_fullStr The localization of centromere protein A is conserved among tissues
title_full_unstemmed The localization of centromere protein A is conserved among tissues
title_short The localization of centromere protein A is conserved among tissues
title_sort localization of centromere protein a is conserved among tissues
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514049/
https://www.ncbi.nlm.nih.gov/pubmed/37735603
http://dx.doi.org/10.1038/s42003-023-05335-7
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