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DNA replication dynamics of vole genome and its epigenetic regulation
BACKGROUND: The genome of some vole rodents exhibit large blocks of heterochromatin coupled to their sex chromosomes. The DNA composition and transcriptional activity of these heterochromatin blocks have been studied, but little is known about their DNA replication dynamics and epigenetic compositio...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6416958/ https://www.ncbi.nlm.nih.gov/pubmed/30871586 http://dx.doi.org/10.1186/s13072-019-0262-0 |
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author | Heinz, Kathrin S. Rapp, Alexander Casas-Delucchi, Corella S. Lehmkuhl, Anne Romero-Fernández, Ismael Sánchez, Antonio Krämer, Oliver H. Marchal, J. Alberto Cardoso, M. Cristina |
author_facet | Heinz, Kathrin S. Rapp, Alexander Casas-Delucchi, Corella S. Lehmkuhl, Anne Romero-Fernández, Ismael Sánchez, Antonio Krämer, Oliver H. Marchal, J. Alberto Cardoso, M. Cristina |
author_sort | Heinz, Kathrin S. |
collection | PubMed |
description | BACKGROUND: The genome of some vole rodents exhibit large blocks of heterochromatin coupled to their sex chromosomes. The DNA composition and transcriptional activity of these heterochromatin blocks have been studied, but little is known about their DNA replication dynamics and epigenetic composition. RESULTS: Here, we show prominent epigenetic marks of the heterochromatic blocks in the giant sex chromosomes of female Microtus cabrerae cells. While the X chromosomes are hypoacetylated and cytosine hypomethylated, they are either enriched for macroH2A and H3K27me3 typical for facultative heterochromatin or for H3K9me3 and HP1 beta typical for constitutive heterochromatin. Using pulse-chase replication labeling and time-lapse microscopy, we found that the heterochromatic block enriched for macroH2A/H3K27me3 of the X chromosome is replicated during mid-S-phase, prior to the heterochromatic block enriched for H3K9me3/HP1 beta, which is replicated during late S-phase. To test whether histone acetylation level regulates its replication dynamics, we induced either global hyperacetylation by pharmacological inhibition or by targeting a histone acetyltransferase to the heterochromatic region of the X chromosomes. Our data reveal that histone acetylation level affects DNA replication dynamics of the sex chromosomes’ heterochromatin and leads to a global reduction in replication fork rate genome wide. CONCLUSIONS: In conclusion, we mapped major epigenetic modifications controlling the structure of the sex chromosome-associated heterochromatin and demonstrated the occurrence of differences in the molecular mechanisms controlling the replication timing of the heterochromatic blocks at the sex chromosomes in female Microtus cabrerae cells. Furthermore, we highlighted a conserved role of histone acetylation level on replication dynamics across mammalian species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13072-019-0262-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6416958 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64169582019-03-25 DNA replication dynamics of vole genome and its epigenetic regulation Heinz, Kathrin S. Rapp, Alexander Casas-Delucchi, Corella S. Lehmkuhl, Anne Romero-Fernández, Ismael Sánchez, Antonio Krämer, Oliver H. Marchal, J. Alberto Cardoso, M. Cristina Epigenetics Chromatin Research BACKGROUND: The genome of some vole rodents exhibit large blocks of heterochromatin coupled to their sex chromosomes. The DNA composition and transcriptional activity of these heterochromatin blocks have been studied, but little is known about their DNA replication dynamics and epigenetic composition. RESULTS: Here, we show prominent epigenetic marks of the heterochromatic blocks in the giant sex chromosomes of female Microtus cabrerae cells. While the X chromosomes are hypoacetylated and cytosine hypomethylated, they are either enriched for macroH2A and H3K27me3 typical for facultative heterochromatin or for H3K9me3 and HP1 beta typical for constitutive heterochromatin. Using pulse-chase replication labeling and time-lapse microscopy, we found that the heterochromatic block enriched for macroH2A/H3K27me3 of the X chromosome is replicated during mid-S-phase, prior to the heterochromatic block enriched for H3K9me3/HP1 beta, which is replicated during late S-phase. To test whether histone acetylation level regulates its replication dynamics, we induced either global hyperacetylation by pharmacological inhibition or by targeting a histone acetyltransferase to the heterochromatic region of the X chromosomes. Our data reveal that histone acetylation level affects DNA replication dynamics of the sex chromosomes’ heterochromatin and leads to a global reduction in replication fork rate genome wide. CONCLUSIONS: In conclusion, we mapped major epigenetic modifications controlling the structure of the sex chromosome-associated heterochromatin and demonstrated the occurrence of differences in the molecular mechanisms controlling the replication timing of the heterochromatic blocks at the sex chromosomes in female Microtus cabrerae cells. Furthermore, we highlighted a conserved role of histone acetylation level on replication dynamics across mammalian species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13072-019-0262-0) contains supplementary material, which is available to authorized users. BioMed Central 2019-03-14 /pmc/articles/PMC6416958/ /pubmed/30871586 http://dx.doi.org/10.1186/s13072-019-0262-0 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Heinz, Kathrin S. Rapp, Alexander Casas-Delucchi, Corella S. Lehmkuhl, Anne Romero-Fernández, Ismael Sánchez, Antonio Krämer, Oliver H. Marchal, J. Alberto Cardoso, M. Cristina DNA replication dynamics of vole genome and its epigenetic regulation |
title | DNA replication dynamics of vole genome and its epigenetic regulation |
title_full | DNA replication dynamics of vole genome and its epigenetic regulation |
title_fullStr | DNA replication dynamics of vole genome and its epigenetic regulation |
title_full_unstemmed | DNA replication dynamics of vole genome and its epigenetic regulation |
title_short | DNA replication dynamics of vole genome and its epigenetic regulation |
title_sort | dna replication dynamics of vole genome and its epigenetic regulation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6416958/ https://www.ncbi.nlm.nih.gov/pubmed/30871586 http://dx.doi.org/10.1186/s13072-019-0262-0 |
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