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An integrative analysis of post-translational histone modifications in the marine diatom Phaeodactylum tricornutum

BACKGROUND: Nucleosomes are the building blocks of chromatin where gene regulation takes place. Chromatin landscapes have been profiled for several species, providing insights into the fundamental mechanisms of chromatin-mediated transcriptional regulation of gene expression. However, knowledge is m...

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Autores principales: Veluchamy, Alaguraj, Rastogi, Achal, Lin, Xin, Lombard, Bérangère, Murik, Omer, Thomas, Yann, Dingli, Florent, Rivarola, Maximo, Ott, Sandra, Liu, Xinyue, Sun, Yezhou, Rabinowicz, Pablo D., McCarthy, James, Allen, Andrew E., Loew, Damarys, Bowler, Chris, Tirichine, Leïla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4504042/
https://www.ncbi.nlm.nih.gov/pubmed/25990474
http://dx.doi.org/10.1186/s13059-015-0671-8
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author Veluchamy, Alaguraj
Rastogi, Achal
Lin, Xin
Lombard, Bérangère
Murik, Omer
Thomas, Yann
Dingli, Florent
Rivarola, Maximo
Ott, Sandra
Liu, Xinyue
Sun, Yezhou
Rabinowicz, Pablo D.
McCarthy, James
Allen, Andrew E.
Loew, Damarys
Bowler, Chris
Tirichine, Leïla
author_facet Veluchamy, Alaguraj
Rastogi, Achal
Lin, Xin
Lombard, Bérangère
Murik, Omer
Thomas, Yann
Dingli, Florent
Rivarola, Maximo
Ott, Sandra
Liu, Xinyue
Sun, Yezhou
Rabinowicz, Pablo D.
McCarthy, James
Allen, Andrew E.
Loew, Damarys
Bowler, Chris
Tirichine, Leïla
author_sort Veluchamy, Alaguraj
collection PubMed
description BACKGROUND: Nucleosomes are the building blocks of chromatin where gene regulation takes place. Chromatin landscapes have been profiled for several species, providing insights into the fundamental mechanisms of chromatin-mediated transcriptional regulation of gene expression. However, knowledge is missing for several major and deep-branching eukaryotic groups, such as the Stramenopiles, which include the diatoms. Diatoms are highly diverse and ubiquitous species of phytoplankton that play a key role in global biogeochemical cycles. Dissecting chromatin-mediated regulation of genes in diatoms will help understand the ecological success of these organisms in contemporary oceans. RESULTS: Here, we use high resolution mass spectrometry to identify a full repertoire of post-translational modifications on histones of the marine diatom Phaeodactylum tricornutum, including eight novel modifications. We map five histone marks coupled with expression data and show that P. tricornutum displays both unique and broadly conserved chromatin features, reflecting the chimeric nature of its genome. Combinatorial analysis of histone marks and DNA methylation demonstrates the presence of an epigenetic code defining activating or repressive chromatin states. We further profile three specific histone marks under conditions of nitrate depletion and show that the histone code is dynamic and targets specific sets of genes. CONCLUSIONS: This study is the first genome-wide characterization of the histone code from a stramenopile and a marine phytoplankton. The work represents an important initial step for understanding the evolutionary history of chromatin and how epigenetic modifications affect gene expression in response to environmental cues in marine environments. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0671-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-45040422015-07-17 An integrative analysis of post-translational histone modifications in the marine diatom Phaeodactylum tricornutum Veluchamy, Alaguraj Rastogi, Achal Lin, Xin Lombard, Bérangère Murik, Omer Thomas, Yann Dingli, Florent Rivarola, Maximo Ott, Sandra Liu, Xinyue Sun, Yezhou Rabinowicz, Pablo D. McCarthy, James Allen, Andrew E. Loew, Damarys Bowler, Chris Tirichine, Leïla Genome Biol Research BACKGROUND: Nucleosomes are the building blocks of chromatin where gene regulation takes place. Chromatin landscapes have been profiled for several species, providing insights into the fundamental mechanisms of chromatin-mediated transcriptional regulation of gene expression. However, knowledge is missing for several major and deep-branching eukaryotic groups, such as the Stramenopiles, which include the diatoms. Diatoms are highly diverse and ubiquitous species of phytoplankton that play a key role in global biogeochemical cycles. Dissecting chromatin-mediated regulation of genes in diatoms will help understand the ecological success of these organisms in contemporary oceans. RESULTS: Here, we use high resolution mass spectrometry to identify a full repertoire of post-translational modifications on histones of the marine diatom Phaeodactylum tricornutum, including eight novel modifications. We map five histone marks coupled with expression data and show that P. tricornutum displays both unique and broadly conserved chromatin features, reflecting the chimeric nature of its genome. Combinatorial analysis of histone marks and DNA methylation demonstrates the presence of an epigenetic code defining activating or repressive chromatin states. We further profile three specific histone marks under conditions of nitrate depletion and show that the histone code is dynamic and targets specific sets of genes. CONCLUSIONS: This study is the first genome-wide characterization of the histone code from a stramenopile and a marine phytoplankton. The work represents an important initial step for understanding the evolutionary history of chromatin and how epigenetic modifications affect gene expression in response to environmental cues in marine environments. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0671-8) contains supplementary material, which is available to authorized users. BioMed Central 2015-05-20 2015 /pmc/articles/PMC4504042/ /pubmed/25990474 http://dx.doi.org/10.1186/s13059-015-0671-8 Text en © Veluchamy et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Veluchamy, Alaguraj
Rastogi, Achal
Lin, Xin
Lombard, Bérangère
Murik, Omer
Thomas, Yann
Dingli, Florent
Rivarola, Maximo
Ott, Sandra
Liu, Xinyue
Sun, Yezhou
Rabinowicz, Pablo D.
McCarthy, James
Allen, Andrew E.
Loew, Damarys
Bowler, Chris
Tirichine, Leïla
An integrative analysis of post-translational histone modifications in the marine diatom Phaeodactylum tricornutum
title An integrative analysis of post-translational histone modifications in the marine diatom Phaeodactylum tricornutum
title_full An integrative analysis of post-translational histone modifications in the marine diatom Phaeodactylum tricornutum
title_fullStr An integrative analysis of post-translational histone modifications in the marine diatom Phaeodactylum tricornutum
title_full_unstemmed An integrative analysis of post-translational histone modifications in the marine diatom Phaeodactylum tricornutum
title_short An integrative analysis of post-translational histone modifications in the marine diatom Phaeodactylum tricornutum
title_sort integrative analysis of post-translational histone modifications in the marine diatom phaeodactylum tricornutum
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4504042/
https://www.ncbi.nlm.nih.gov/pubmed/25990474
http://dx.doi.org/10.1186/s13059-015-0671-8
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