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Viral proteins as a potential driver of histone depletion in dinoflagellates
Within canonical eukaryotic nuclei, DNA is packaged with highly conserved histone proteins into nucleosomes, which facilitate DNA condensation and contribute to genomic regulation. Yet the dinoflagellates, a group of unicellular algae, are a striking exception to this otherwise universal feature as...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5906630/ https://www.ncbi.nlm.nih.gov/pubmed/29670105 http://dx.doi.org/10.1038/s41467-018-03993-4 |
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author | Irwin, Nicholas A. T. Martin, Benjamin J. E. Young, Barry P. Browne, Martin J. G. Flaus, Andrew Loewen, Christopher J. R. Keeling, Patrick J. Howe, LeAnn J. |
author_facet | Irwin, Nicholas A. T. Martin, Benjamin J. E. Young, Barry P. Browne, Martin J. G. Flaus, Andrew Loewen, Christopher J. R. Keeling, Patrick J. Howe, LeAnn J. |
author_sort | Irwin, Nicholas A. T. |
collection | PubMed |
description | Within canonical eukaryotic nuclei, DNA is packaged with highly conserved histone proteins into nucleosomes, which facilitate DNA condensation and contribute to genomic regulation. Yet the dinoflagellates, a group of unicellular algae, are a striking exception to this otherwise universal feature as they have largely abandoned histones and acquired apparently viral-derived substitutes termed DVNPs (dinoflagellate-viral-nucleoproteins). Despite the magnitude of this transition, its evolutionary drivers remain unknown. Here, using Saccharomyces cerevisiae as a model, we show that DVNP impairs growth and antagonizes chromatin by localizing to histone binding sites, displacing nucleosomes, and impairing transcription. Furthermore, DVNP toxicity can be relieved through histone depletion and cells diminish their histones in response to DVNP expression suggesting that histone reduction could have been an adaptive response to these viral proteins. These findings provide insights into eukaryotic chromatin evolution and highlight the potential for horizontal gene transfer to drive the divergence of cellular systems. |
format | Online Article Text |
id | pubmed-5906630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59066302018-04-20 Viral proteins as a potential driver of histone depletion in dinoflagellates Irwin, Nicholas A. T. Martin, Benjamin J. E. Young, Barry P. Browne, Martin J. G. Flaus, Andrew Loewen, Christopher J. R. Keeling, Patrick J. Howe, LeAnn J. Nat Commun Article Within canonical eukaryotic nuclei, DNA is packaged with highly conserved histone proteins into nucleosomes, which facilitate DNA condensation and contribute to genomic regulation. Yet the dinoflagellates, a group of unicellular algae, are a striking exception to this otherwise universal feature as they have largely abandoned histones and acquired apparently viral-derived substitutes termed DVNPs (dinoflagellate-viral-nucleoproteins). Despite the magnitude of this transition, its evolutionary drivers remain unknown. Here, using Saccharomyces cerevisiae as a model, we show that DVNP impairs growth and antagonizes chromatin by localizing to histone binding sites, displacing nucleosomes, and impairing transcription. Furthermore, DVNP toxicity can be relieved through histone depletion and cells diminish their histones in response to DVNP expression suggesting that histone reduction could have been an adaptive response to these viral proteins. These findings provide insights into eukaryotic chromatin evolution and highlight the potential for horizontal gene transfer to drive the divergence of cellular systems. Nature Publishing Group UK 2018-04-18 /pmc/articles/PMC5906630/ /pubmed/29670105 http://dx.doi.org/10.1038/s41467-018-03993-4 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Irwin, Nicholas A. T. Martin, Benjamin J. E. Young, Barry P. Browne, Martin J. G. Flaus, Andrew Loewen, Christopher J. R. Keeling, Patrick J. Howe, LeAnn J. Viral proteins as a potential driver of histone depletion in dinoflagellates |
title | Viral proteins as a potential driver of histone depletion in dinoflagellates |
title_full | Viral proteins as a potential driver of histone depletion in dinoflagellates |
title_fullStr | Viral proteins as a potential driver of histone depletion in dinoflagellates |
title_full_unstemmed | Viral proteins as a potential driver of histone depletion in dinoflagellates |
title_short | Viral proteins as a potential driver of histone depletion in dinoflagellates |
title_sort | viral proteins as a potential driver of histone depletion in dinoflagellates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5906630/ https://www.ncbi.nlm.nih.gov/pubmed/29670105 http://dx.doi.org/10.1038/s41467-018-03993-4 |
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