Gcn5‐dependent histone H3 acetylation and gene activity is required for the asexual development and virulence of Beauveria bassiana

Summary Gcn5 is a core histone acetyltransferase that catalyzes histone H3 acetylation on N‐terminal lysine residues in yeasts and was reported to catalyze H3K9/K14 acetylation required for activating asexual development in Aspergillus . Here, we report a localization of Gcn5 ortholog in the nucleus and cytoplasm of Beauveria bassiana , a fungal insect pathogen. Deletion of gcn5 led to hypoacetylated H3 at K9/14/18/27 and 97% reduction in conidiation capacity as well as severe defects in colony growth and conidial thermotolerance. Two master conidiation genes, namely brlA and abaA , were transcriptionally repressed to undetectable level in Δ gcn5 , but sharply upregulated in wild‐type, at the beginning time of conidiation. Based on chromatin immunoprecipitation, both DNA and acetylation levels of the distal and proximal fragments of the brlA promoter bound by acetylated H3K14 alone were upregulated in wild‐type, but not in Δ gcn5 , at the mentioned time. In Δ gcn5 , normal cuticle infection was abolished while virulence through cuticle‐bypassing infection was greatly attenuated, accompanied by drastically reduced activities of putative cuticle‐degrading enzymes, retarded dimorphic transition and transcriptional repression of associated genes. These findings unveil a novel mechanism by which Gcn5 activates asexual development pathway by acetylating H3K14 and regulates the virulence‐related cellular events in B. bassiana .