Replisome function during replicative stress is modulated by histone h3 lysine 56 acetylation through Ctf4

• Published in: Genetics (Austin) Vol. 199; no. 4; pp. 1047 - 1063
• Main Authors: Luciano, Pierre, Dehé, Pierre-Marie, Audebert, Stéphane, Géli, Vincent, Corda, Yves
• Format: Journal Article
• Language: English
• Published: United States Genetics Society of America 01.04.2015
• Subjects: Acetylation; Cullin Proteins - genetics; Cullin Proteins - metabolism; Deoxyribonucleic acid; DNA; DNA-Binding Proteins - genetics; DNA-Binding Proteins - metabolism; DNA-Directed DNA Polymerase - genetics; DNA-Directed DNA Polymerase - metabolism; Genomes; Histones - metabolism; Investigations; Lysine - metabolism; Multienzyme Complexes - genetics; Multienzyme Complexes - metabolism; Nuclear Proteins - genetics; Nuclear Proteins - metabolism; Protein Processing, Post-Translational; Proteins; Saccharomyces cerevisiae; Saccharomyces cerevisiae - genetics; Saccharomyces cerevisiae Proteins - genetics; Saccharomyces cerevisiae Proteins - metabolism; Scientific imaging; Stress; H3K56 acetylation; Mms22; replisome; replicative stress; Ctf4
• ISSN: 1943-2631; 0016-6731; 1943-2631
• DOI: 10.1534/genetics.114.173856

Histone H3 lysine 56 acetylation in Saccharomyces cerevisiae is required for the maintenance of genome stability under normal conditions and upon DNA replication stress. Here we show that in the absence of H3 lysine 56 acetylation replisome components become deleterious when replication forks collapse at natural replication block sites. This lethality is not a direct consequence of chromatin assembly defects during replication fork progression. Rather, our genetic analyses suggest that in the presence of replicative stress H3 lysine 56 acetylation uncouples the Cdc45-Mcm2-7-GINS DNA helicase complex and DNA polymerases through the replisome component Ctf4. In addition, we discovered that the N-terminal domain of Ctf4, necessary for the interaction of Ctf4 with Mms22, an adaptor protein of the Rtt101-Mms1 E3 ubiquitin ligase, is required for the function of the H3 lysine 56 acetylation pathway, suggesting that replicative stress promotes the interaction between Ctf4 and Mms22. Taken together, our results indicate that Ctf4 is an essential member of the H3 lysine 56 acetylation pathway and provide novel mechanistic insights into understanding the role of H3 lysine 56 acetylation in maintaining genome stability upon replication stress.