Abstract
In eukaryotic organisms, histones are dynamically exchanged independently of DNA replication. Recent reports show that different coding regions differ in their amount of replication-independent histone H3 exchange. The current paradigm is that this histone exchange variability among coding regions is a consequence of transcription rate. Here we put forward the idea that this variability might be also modulated in a gene-specific manner independently of transcription rate. To that end, we study transcription rate-independent replication-independent coding region histone H3 exchange. We term such events relative exchange. Our genome-wide analysis shows conclusively that in yeast, relative exchange is a novel consistent feature of coding regions. Outside of replication, each coding region has a characteristic pattern of histone H3 exchange that is either higher or lower than what was expected by its RNAPII transcription rate alone. Histone H3 exchange in coding regions might be a way to add or remove certain histone modifications that are important for transcription elongation. Therefore, our results that gene-specific coding region histone H3 exchange is decoupled from transcription rate might hint at a new epigenetic mechanism of transcription regulation.
MeSH Terms
Cell Cycle Proteins
Chromatin Assembly and Disassembly/genetics
DNA Repair/physiology
DNA Replication/physiology
Epigenesis, Genetic/physiology
Genome, Fungal
Histones/genetics,metabolism
Molecular Chaperones
Open Reading Frames
Protein Processing, Post-Translational/genetics
Saccharomyces cerevisiae/genetics,metabolism
Saccharomyces cerevisiae Proteins
Transcription, Genetic
Chemicals
ASF1 protein, S cerevisiae
Cell Cycle Proteins
Histones
Molecular Chaperones
Saccharomyces cerevisiae Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Gat-Viks Irit
Computational Molecular Biology Department, Max Planck Institute for Molecular Genetics, Berlin, Germany.
[email protected]
Vingron Martin
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