Catalytic-Site Mutations in the MYST Family Histone Acetyltransferase Esa1

• DOI: 10.1534/genetics.107.080135
• Publication Date: 2008-02-02T02:07:40Z
• Authors: Peter V Decker; David Y Yu; Masayoshi Iizuka; Qifeng Qiu; M Mitchell Smith
• Keywords: 0301 basic medicine; Microbial Viability; Saccharomyces cerevisiae Proteins; Models, Genetic; Blotting, Western; Saccharomyces cerevisiae; Protein Structure, Secondary; Recombinant Proteins; 03 medical and health sciences; Phenotype; Catalytic Domain; Mutation; Alleles; Histone Acetyltransferases

AbstractEsa1 is the only essential histone acetyltransferase (HAT) in budding yeast. It is the catalytic subunit of at least two multiprotein complexes, NuA4 and Piccolo NuA4 (picNuA4), and its essential function is believed to be its catalytic HAT activity. To examine the role of Esa1 in DNA damage repair, we isolated viable esa1 mutants with a range of hypersensitivities to the toposide camptothecin. Here we show that the sensitivity of these mutants to a variety of stresses is inversely proportional to their level of histone H4 acetylation, demonstrating the importance of Esa1 catalytic activity for resistance to genotoxic stress. Surprisingly, individual mutations in two residues directly involved in catalysis were not lethal even though the mutant enzymes appear catalytically inactive both in vivo and in vitro. However, the double-point mutant is lethal, demonstrating that the essential function of Esa1 relies on residues within the catalytic pocket but not catalysis. We propose that the essential function of Esa1 may be to bind acetyl-CoA or lysine substrates and positively regulate the activities of NuA4 and Piccolo NuA4.