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H3K79 methylation: a new conserved mark that accompanies H4 hyperacetylation prior to histone-to-protamine transition in Drosophila and rat
Author(s) -
Christine Dottermusch-Heidel,
Stefanie Gärtner,
Isabel Tegeder,
Christina Rathke,
Bridlin Barckmann,
Marek Bartkuhn,
Sudhanshu Bhushan,
Klaus Steger,
Andreas Meinhardt,
Renate RenkawitzPohl
Publication year - 2014
Publication title -
biology open
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.936
H-Index - 41
ISSN - 2046-6390
DOI - 10.1242/bio.20147302
Subject(s) - biology , protamine , chromatin , histone , histone methyltransferase , histone h4 , histone methylation , chromatin remodeling , histone h2a , ezh2 , histone h1 , histone code , microbiology and biotechnology , acetylation , genetics , dna methylation , biochemistry , nucleosome , dna , gene expression , gene , heparin
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.

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