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Dynamic methylation of histone H3K18 in differentiating Theileria parasites
Lysine methylation on histone tails impacts genome regulation and cell fate determination in many developmental processes. Apicomplexa intracellular parasites cause major diseases and they have developed complex life cycles with fine-tuned differentiation events. Yet, apicomplexa genomes have few tr...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8163883/ https://www.ncbi.nlm.nih.gov/pubmed/34050145 http://dx.doi.org/10.1038/s41467-021-23477-2 |
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author | Cheeseman, Kevin Jannot, Guillaume Lourenço, Nelly Villares, Marie Berthelet, Jérémy Calegari-Silva, Teresa Hamroune, Juliette Letourneur, Franck Rodrigues-Lima, Fernando Weitzman, Jonathan B. |
author_facet | Cheeseman, Kevin Jannot, Guillaume Lourenço, Nelly Villares, Marie Berthelet, Jérémy Calegari-Silva, Teresa Hamroune, Juliette Letourneur, Franck Rodrigues-Lima, Fernando Weitzman, Jonathan B. |
author_sort | Cheeseman, Kevin |
collection | PubMed |
description | Lysine methylation on histone tails impacts genome regulation and cell fate determination in many developmental processes. Apicomplexa intracellular parasites cause major diseases and they have developed complex life cycles with fine-tuned differentiation events. Yet, apicomplexa genomes have few transcription factors and little is known about their epigenetic control systems. Tick-borne Theileria apicomplexa species have relatively small, compact genomes and a remarkable ability to transform leucocytes in their bovine hosts. Here we report enriched H3 lysine 18 monomethylation (H3K18me1) on the gene bodies of repressed genes in Theileria macroschizonts. Differentiation to merozoites (merogony) leads to decreased H3K18me1 in parasite nuclei. Pharmacological manipulation of H3K18 acetylation or methylation impacted parasite differentiation and expression of stage-specific genes. Finally, we identify a parasite SET-domain methyltransferase (TaSETup1) that can methylate H3K18 and represses gene expression. Thus, H3K18me1 emerges as an important epigenetic mark which controls gene expression and stage differentiation in Theileria parasites. |
format | Online Article Text |
id | pubmed-8163883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81638832021-06-11 Dynamic methylation of histone H3K18 in differentiating Theileria parasites Cheeseman, Kevin Jannot, Guillaume Lourenço, Nelly Villares, Marie Berthelet, Jérémy Calegari-Silva, Teresa Hamroune, Juliette Letourneur, Franck Rodrigues-Lima, Fernando Weitzman, Jonathan B. Nat Commun Article Lysine methylation on histone tails impacts genome regulation and cell fate determination in many developmental processes. Apicomplexa intracellular parasites cause major diseases and they have developed complex life cycles with fine-tuned differentiation events. Yet, apicomplexa genomes have few transcription factors and little is known about their epigenetic control systems. Tick-borne Theileria apicomplexa species have relatively small, compact genomes and a remarkable ability to transform leucocytes in their bovine hosts. Here we report enriched H3 lysine 18 monomethylation (H3K18me1) on the gene bodies of repressed genes in Theileria macroschizonts. Differentiation to merozoites (merogony) leads to decreased H3K18me1 in parasite nuclei. Pharmacological manipulation of H3K18 acetylation or methylation impacted parasite differentiation and expression of stage-specific genes. Finally, we identify a parasite SET-domain methyltransferase (TaSETup1) that can methylate H3K18 and represses gene expression. Thus, H3K18me1 emerges as an important epigenetic mark which controls gene expression and stage differentiation in Theileria parasites. Nature Publishing Group UK 2021-05-28 /pmc/articles/PMC8163883/ /pubmed/34050145 http://dx.doi.org/10.1038/s41467-021-23477-2 Text en © The Author(s) 2021 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 Cheeseman, Kevin Jannot, Guillaume Lourenço, Nelly Villares, Marie Berthelet, Jérémy Calegari-Silva, Teresa Hamroune, Juliette Letourneur, Franck Rodrigues-Lima, Fernando Weitzman, Jonathan B. Dynamic methylation of histone H3K18 in differentiating Theileria parasites |
title | Dynamic methylation of histone H3K18 in differentiating Theileria parasites |
title_full | Dynamic methylation of histone H3K18 in differentiating Theileria parasites |
title_fullStr | Dynamic methylation of histone H3K18 in differentiating Theileria parasites |
title_full_unstemmed | Dynamic methylation of histone H3K18 in differentiating Theileria parasites |
title_short | Dynamic methylation of histone H3K18 in differentiating Theileria parasites |
title_sort | dynamic methylation of histone h3k18 in differentiating theileria parasites |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8163883/ https://www.ncbi.nlm.nih.gov/pubmed/34050145 http://dx.doi.org/10.1038/s41467-021-23477-2 |
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