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The Mi-2 nucleosome remodeler and the Rpd3 histone deacetylase are involved in piRNA-guided heterochromatin formation
In eukaryotes, trimethylation of lysine 9 on histone H3 (H3K9) is associated with transcriptional silencing of transposable elements (TEs). In drosophila ovaries, this heterochromatic repressive mark is thought to be deposited by SetDB1 on TE genomic loci after the initial recognition of nascent tra...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7272611/ https://www.ncbi.nlm.nih.gov/pubmed/32499524 http://dx.doi.org/10.1038/s41467-020-16635-5 |
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author | Mugat, Bruno Nicot, Simon Varela-Chavez, Carolina Jourdan, Christophe Sato, Kaoru Basyuk, Eugenia Juge, François Siomi, Mikiko C. Pélisson, Alain Chambeyron, Séverine |
author_facet | Mugat, Bruno Nicot, Simon Varela-Chavez, Carolina Jourdan, Christophe Sato, Kaoru Basyuk, Eugenia Juge, François Siomi, Mikiko C. Pélisson, Alain Chambeyron, Séverine |
author_sort | Mugat, Bruno |
collection | PubMed |
description | In eukaryotes, trimethylation of lysine 9 on histone H3 (H3K9) is associated with transcriptional silencing of transposable elements (TEs). In drosophila ovaries, this heterochromatic repressive mark is thought to be deposited by SetDB1 on TE genomic loci after the initial recognition of nascent transcripts by PIWI-interacting RNAs (piRNAs) loaded on the Piwi protein. Here, we show that the nucleosome remodeler Mi-2, in complex with its partner MEP-1, forms a subunit that is transiently associated, in a MEP-1 C-terminus-dependent manner, with known Piwi interactors, including a recently reported SUMO ligase, Su(var)2-10. Together with the histone deacetylase Rpd3, this module is involved in the piRNA-dependent TE silencing, correlated with H3K9 deacetylation and trimethylation. Therefore, drosophila piRNA-mediated transcriptional silencing involves three epigenetic effectors, a remodeler, Mi-2, an eraser, Rpd3 and a writer, SetDB1, in addition to the Su(var)2-10 SUMO ligase. |
format | Online Article Text |
id | pubmed-7272611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72726112020-06-15 The Mi-2 nucleosome remodeler and the Rpd3 histone deacetylase are involved in piRNA-guided heterochromatin formation Mugat, Bruno Nicot, Simon Varela-Chavez, Carolina Jourdan, Christophe Sato, Kaoru Basyuk, Eugenia Juge, François Siomi, Mikiko C. Pélisson, Alain Chambeyron, Séverine Nat Commun Article In eukaryotes, trimethylation of lysine 9 on histone H3 (H3K9) is associated with transcriptional silencing of transposable elements (TEs). In drosophila ovaries, this heterochromatic repressive mark is thought to be deposited by SetDB1 on TE genomic loci after the initial recognition of nascent transcripts by PIWI-interacting RNAs (piRNAs) loaded on the Piwi protein. Here, we show that the nucleosome remodeler Mi-2, in complex with its partner MEP-1, forms a subunit that is transiently associated, in a MEP-1 C-terminus-dependent manner, with known Piwi interactors, including a recently reported SUMO ligase, Su(var)2-10. Together with the histone deacetylase Rpd3, this module is involved in the piRNA-dependent TE silencing, correlated with H3K9 deacetylation and trimethylation. Therefore, drosophila piRNA-mediated transcriptional silencing involves three epigenetic effectors, a remodeler, Mi-2, an eraser, Rpd3 and a writer, SetDB1, in addition to the Su(var)2-10 SUMO ligase. Nature Publishing Group UK 2020-06-04 /pmc/articles/PMC7272611/ /pubmed/32499524 http://dx.doi.org/10.1038/s41467-020-16635-5 Text en © The Author(s) 2020 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 Mugat, Bruno Nicot, Simon Varela-Chavez, Carolina Jourdan, Christophe Sato, Kaoru Basyuk, Eugenia Juge, François Siomi, Mikiko C. Pélisson, Alain Chambeyron, Séverine The Mi-2 nucleosome remodeler and the Rpd3 histone deacetylase are involved in piRNA-guided heterochromatin formation |
title | The Mi-2 nucleosome remodeler and the Rpd3 histone deacetylase are involved in piRNA-guided heterochromatin formation |
title_full | The Mi-2 nucleosome remodeler and the Rpd3 histone deacetylase are involved in piRNA-guided heterochromatin formation |
title_fullStr | The Mi-2 nucleosome remodeler and the Rpd3 histone deacetylase are involved in piRNA-guided heterochromatin formation |
title_full_unstemmed | The Mi-2 nucleosome remodeler and the Rpd3 histone deacetylase are involved in piRNA-guided heterochromatin formation |
title_short | The Mi-2 nucleosome remodeler and the Rpd3 histone deacetylase are involved in piRNA-guided heterochromatin formation |
title_sort | mi-2 nucleosome remodeler and the rpd3 histone deacetylase are involved in pirna-guided heterochromatin formation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7272611/ https://www.ncbi.nlm.nih.gov/pubmed/32499524 http://dx.doi.org/10.1038/s41467-020-16635-5 |
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