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H3K79 methylation: a new conserved mark that accompanies H4 hyperacetylation prior to histone-to-protamine transition in Drosophila and rat
During spermiogenesis, haploid spermatids undergo extensive chromatin remodeling events in which histones are successively replaced by more basic protamines to generate highly compacted chromatin. Here we show for the first time that H3K79 methylation is a conserved feature preceding the histone-to-...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058078/ https://www.ncbi.nlm.nih.gov/pubmed/24795146 http://dx.doi.org/10.1242/bio.20147302 |
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author | Dottermusch-Heidel, Christine Gärtner, Stefanie M. K. Tegeder, Isabel Rathke, Christina Barckmann, Bridlin Bartkuhn, Marek Bhushan, Sudhanshu Steger, Klaus Meinhardt, Andreas Renkawitz-Pohl, Renate |
author_facet | Dottermusch-Heidel, Christine Gärtner, Stefanie M. K. Tegeder, Isabel Rathke, Christina Barckmann, Bridlin Bartkuhn, Marek Bhushan, Sudhanshu Steger, Klaus Meinhardt, Andreas Renkawitz-Pohl, Renate |
author_sort | Dottermusch-Heidel, Christine |
collection | PubMed |
description | During spermiogenesis, haploid spermatids undergo extensive chromatin remodeling events in which histones are successively replaced by more basic protamines to generate highly compacted chromatin. Here we show for the first time that H3K79 methylation is a conserved feature preceding the histone-to-protamine transition in Drosophila melanogaster and rat. During Drosophila spermatogenesis, the Dot1-like methyltransferase Grappa (Gpp) is primarily expressed in canoe stage nuclei. The corresponding H3K79 methylation is a histone modification that precedes the histone-to-protamine transition and correlates with histone H4 hyperacetylation. When acetylation was inhibited in cultured Drosophila testes, nuclei were smaller and chromatin was compact, Gpp was little synthesized, H3K79 methylation was strongly reduced, and protamines were not synthesized. The Gpp isoform Gpp-D has a unique C-terminus, and Gpp is essential for full fertility. In rat, H3K79 methylation also correlates with H4 hyperacetylation but not with active RNA polymerase II, which might point towards a conserved function in chromatin remodeling during the histone-to-protamine transition in both Drosophila and rat. |
format | Online Article Text |
id | pubmed-4058078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Company of Biologists |
record_format | MEDLINE/PubMed |
spelling | pubmed-40580782014-07-15 H3K79 methylation: a new conserved mark that accompanies H4 hyperacetylation prior to histone-to-protamine transition in Drosophila and rat Dottermusch-Heidel, Christine Gärtner, Stefanie M. K. Tegeder, Isabel Rathke, Christina Barckmann, Bridlin Bartkuhn, Marek Bhushan, Sudhanshu Steger, Klaus Meinhardt, Andreas Renkawitz-Pohl, Renate Biol Open Research Article During spermiogenesis, haploid spermatids undergo extensive chromatin remodeling events in which histones are successively replaced by more basic protamines to generate highly compacted chromatin. Here we show for the first time that H3K79 methylation is a conserved feature preceding the histone-to-protamine transition in Drosophila melanogaster and rat. During Drosophila spermatogenesis, the Dot1-like methyltransferase Grappa (Gpp) is primarily expressed in canoe stage nuclei. The corresponding H3K79 methylation is a histone modification that precedes the histone-to-protamine transition and correlates with histone H4 hyperacetylation. When acetylation was inhibited in cultured Drosophila testes, nuclei were smaller and chromatin was compact, Gpp was little synthesized, H3K79 methylation was strongly reduced, and protamines were not synthesized. The Gpp isoform Gpp-D has a unique C-terminus, and Gpp is essential for full fertility. In rat, H3K79 methylation also correlates with H4 hyperacetylation but not with active RNA polymerase II, which might point towards a conserved function in chromatin remodeling during the histone-to-protamine transition in both Drosophila and rat. The Company of Biologists 2014-05-02 /pmc/articles/PMC4058078/ /pubmed/24795146 http://dx.doi.org/10.1242/bio.20147302 Text en © 2014. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Dottermusch-Heidel, Christine Gärtner, Stefanie M. K. Tegeder, Isabel Rathke, Christina Barckmann, Bridlin Bartkuhn, Marek Bhushan, Sudhanshu Steger, Klaus Meinhardt, Andreas Renkawitz-Pohl, Renate H3K79 methylation: a new conserved mark that accompanies H4 hyperacetylation prior to histone-to-protamine transition in Drosophila and rat |
title | H3K79 methylation: a new conserved mark that accompanies H4 hyperacetylation prior to histone-to-protamine transition in Drosophila and rat |
title_full | H3K79 methylation: a new conserved mark that accompanies H4 hyperacetylation prior to histone-to-protamine transition in Drosophila and rat |
title_fullStr | H3K79 methylation: a new conserved mark that accompanies H4 hyperacetylation prior to histone-to-protamine transition in Drosophila and rat |
title_full_unstemmed | H3K79 methylation: a new conserved mark that accompanies H4 hyperacetylation prior to histone-to-protamine transition in Drosophila and rat |
title_short | H3K79 methylation: a new conserved mark that accompanies H4 hyperacetylation prior to histone-to-protamine transition in Drosophila and rat |
title_sort | h3k79 methylation: a new conserved mark that accompanies h4 hyperacetylation prior to histone-to-protamine transition in drosophila and rat |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058078/ https://www.ncbi.nlm.nih.gov/pubmed/24795146 http://dx.doi.org/10.1242/bio.20147302 |
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