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Histone modifications during the life cycle of the brown alga Ectocarpus
BACKGROUND: Brown algae evolved complex multicellularity independently of the animal and land plant lineages and are the third most developmentally complex phylogenetic group on the planet. An understanding of developmental processes in this group is expected to provide important insights into the e...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784034/ https://www.ncbi.nlm.nih.gov/pubmed/33397407 http://dx.doi.org/10.1186/s13059-020-02216-8 |
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author | Bourdareau, Simon Tirichine, Leila Lombard, Bérangère Loew, Damarys Scornet, Delphine Wu, Yue Coelho, Susana M. Cock, J. Mark |
author_facet | Bourdareau, Simon Tirichine, Leila Lombard, Bérangère Loew, Damarys Scornet, Delphine Wu, Yue Coelho, Susana M. Cock, J. Mark |
author_sort | Bourdareau, Simon |
collection | PubMed |
description | BACKGROUND: Brown algae evolved complex multicellularity independently of the animal and land plant lineages and are the third most developmentally complex phylogenetic group on the planet. An understanding of developmental processes in this group is expected to provide important insights into the evolutionary events necessary for the emergence of complex multicellularity. Here, we focus on mechanisms of epigenetic regulation involving post-translational modifications of histone proteins. RESULTS: A total of 47 histone post-translational modifications are identified, including a novel mark H2AZR38me1, but Ectocarpus lacks both H3K27me3 and the major polycomb complexes. ChIP-seq identifies modifications associated with transcription start sites and gene bodies of active genes and with transposons. H3K79me2 exhibits an unusual pattern, often marking large genomic regions spanning several genes. Transcription start sites of closely spaced, divergently transcribed gene pairs share a common nucleosome-depleted region and exhibit shared histone modification peaks. Overall, patterns of histone modifications are stable through the life cycle. Analysis of histone modifications at generation-biased genes identifies a correlation between the presence of specific chromatin marks and the level of gene expression. CONCLUSIONS: The overview of histone post-translational modifications in the brown alga presented here will provide a foundation for future studies aimed at understanding the role of chromatin modifications in the regulation of brown algal genomes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-020-02216-8. |
format | Online Article Text |
id | pubmed-7784034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77840342021-01-14 Histone modifications during the life cycle of the brown alga Ectocarpus Bourdareau, Simon Tirichine, Leila Lombard, Bérangère Loew, Damarys Scornet, Delphine Wu, Yue Coelho, Susana M. Cock, J. Mark Genome Biol Research BACKGROUND: Brown algae evolved complex multicellularity independently of the animal and land plant lineages and are the third most developmentally complex phylogenetic group on the planet. An understanding of developmental processes in this group is expected to provide important insights into the evolutionary events necessary for the emergence of complex multicellularity. Here, we focus on mechanisms of epigenetic regulation involving post-translational modifications of histone proteins. RESULTS: A total of 47 histone post-translational modifications are identified, including a novel mark H2AZR38me1, but Ectocarpus lacks both H3K27me3 and the major polycomb complexes. ChIP-seq identifies modifications associated with transcription start sites and gene bodies of active genes and with transposons. H3K79me2 exhibits an unusual pattern, often marking large genomic regions spanning several genes. Transcription start sites of closely spaced, divergently transcribed gene pairs share a common nucleosome-depleted region and exhibit shared histone modification peaks. Overall, patterns of histone modifications are stable through the life cycle. Analysis of histone modifications at generation-biased genes identifies a correlation between the presence of specific chromatin marks and the level of gene expression. CONCLUSIONS: The overview of histone post-translational modifications in the brown alga presented here will provide a foundation for future studies aimed at understanding the role of chromatin modifications in the regulation of brown algal genomes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-020-02216-8. BioMed Central 2021-01-04 /pmc/articles/PMC7784034/ /pubmed/33397407 http://dx.doi.org/10.1186/s13059-020-02216-8 Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Bourdareau, Simon Tirichine, Leila Lombard, Bérangère Loew, Damarys Scornet, Delphine Wu, Yue Coelho, Susana M. Cock, J. Mark Histone modifications during the life cycle of the brown alga Ectocarpus |
title | Histone modifications during the life cycle of the brown alga Ectocarpus |
title_full | Histone modifications during the life cycle of the brown alga Ectocarpus |
title_fullStr | Histone modifications during the life cycle of the brown alga Ectocarpus |
title_full_unstemmed | Histone modifications during the life cycle of the brown alga Ectocarpus |
title_short | Histone modifications during the life cycle of the brown alga Ectocarpus |
title_sort | histone modifications during the life cycle of the brown alga ectocarpus |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784034/ https://www.ncbi.nlm.nih.gov/pubmed/33397407 http://dx.doi.org/10.1186/s13059-020-02216-8 |
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