Histone degradation in response to DNA damage enhances chromatin dynamics and recombination rates.
Nucleosomes are essential for proper chromatin organization and the maintenance of genome integrity. Histones are post-translationally modified and often evicted at sites of DNA breaks, facilitating the recruitment of repair factors. Whether such chromatin changes are localized or genome-wide is debated. Here we show that cellular levels of histones drop ... 20-40% in response to DNA damage. This histone loss occurs from chromatin, is proteasome-mediated and requires both the DNA damage checkpoint and the INO80 nucleosome remodeler. We confirmed reductions in histone levels by stable isotope labeling of amino acids in cell culture (SILAC)-based mass spectrometry, genome-wide nucleosome mapping and fluorescence microscopy. Chromatin decompaction and increased fiber flexibility accompanied histone degradation, both in response to DNA damage and after artificial reduction of histone levels. As a result, recombination rates and DNA-repair focus turnover were enhanced. Thus, we propose that a generalized reduction in nucleosome occupancy is an integral part of the DNA damage response in yeast that provides mechanisms for enhanced chromatin mobility and homology search.
Mesh Terms:
Chromatin, Chromatin Assembly and Disassembly, DNA Damage, DNA Repair, Histones, Proteasome Endopeptidase Complex, Proteolysis, Recombination, Genetic, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins
Chromatin, Chromatin Assembly and Disassembly, DNA Damage, DNA Repair, Histones, Proteasome Endopeptidase Complex, Proteolysis, Recombination, Genetic, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins
Nat. Struct. Mol. Biol.
Date: Feb. 01, 2017
PubMed ID: 28067915
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