NuA4 Initiates Dynamic Histone H4 Acetylation to Promote High-Fidelity Sister Chromatid Recombination at Postreplication Gaps

• Published in: Molecular cell 2014-09, Vol.55 (6), p.818-828
• Main Authors: House, Nealia C.M., Yang, Jiahui H., Walsh, Stephen C., Moy, Jonathan M., Freudenreich, Catherine H.
• Format: Article
• Language: English
• Subjects: Acetylation; Chromatin Assembly and Disassembly; Chromosomes, Fungal; DNA Damage; DNA Repair; DNA Replication; Genome, Fungal; Genomic Instability; Histone Acetyltransferases - genetics; Histone Acetyltransferases - metabolism; Histone Deacetylases - genetics; Histone Deacetylases - metabolism; Histones - metabolism; Saccharomyces cerevisiae - enzymology; Saccharomyces cerevisiae - genetics; Saccharomyces cerevisiae Proteins - genetics; Saccharomyces cerevisiae Proteins - metabolism; Sister Chromatid Exchange; Trinucleotide Repeats - genetics
• ISSN: 1097-2765; 1097-4164
• DOI: 10.1016/j.molcel.2014.07.007

CAG/CTG trinucleotide repeats are unstable, fragile sequences that strongly position nucleosomes, but little is known about chromatin modifications required to prevent genomic instability at these or other structure-forming sequences. We discovered that regulated histone H4 acetylation is required to maintain CAG repeat stability and promote gap-induced sister chromatid recombination. CAG expansions in the absence of H4 HATs NuA4 and Hat1 and HDACs Sir2, Hos2, and Hst1 depended on Rad52, Rad57, and Rad5 and were therefore arising through homology-mediated postreplication repair (PRR) events. H4K12 and H4K16 acetylation were required to prevent Rad5-dependent CAG repeat expansions, and H4K16 acetylation was enriched at CAG repeats during S phase. Genetic experiments placed the RSC chromatin remodeler in the same PRR pathway, and Rsc2 recruitment was coincident with H4K16 acetylation. Here we have utilized a repetitive DNA sequence that induces endogenous DNA damage to identify histone modifications that regulate recombination efficiency and fidelity during postreplication gap repair. [Display omitted] •H4 HATs and HDACs promote postreplication HR repair to prevent CAG repeat expansions•Histone H4K16 acetylation is enriched during S phase at an expanded CAG repeat tract•Gap-induced sister chromatid recombination requires H4K16ac and Esa1 of NuA4•The RSC2 remodeler contributes to gap repair and fidelity of template switch events CAG repeats expand to cause disease and create site-specific replication and repair difficulties due to the formation of hairpin structures. House et al. show that acetylation of histone H4 lysines 12 and 16 and RSC2 remodeling are important for preventing CAG expansions by promoting fidelity of postreplication gap repair.