A MYST family histone acetyltransferase, MoSAS3, is required for development and pathogenicity in the rice blast fungus

Mol Plant Pathol. 2019 Nov;20(11):1491-1505. doi: 10.1111/mpp.12856. Epub 2019 Jul 30.

Abstract

Histone acetylation has been established as a principal epigenetic regulatory mechanism in eukaryotes. Sas3, a histone acetyltransferase belonging to the largest family of acetyltransferase, MYST, is the catalytic subunit of a conserved histone acetyltransferase complex. To date, the functions of Sas3 and its orthologues have been extensively studied in yeast, humans and flies in relation to global acetylation and transcriptional regulation. However, its precise impact on development and pathogenicity in fungal plant pathogens has yet to be elucidated. Considering the importance of Sas3 in H3K14 acetylation, here we investigate the roles of its orthologue in the rice blast fungus, Magnaporthe oryzae (Pyricularia oryzae). Unlike a previously reported Sas3 deletion in yeast, which led to no remarkable phenotypic changes, we found that MoSAS3 deletion alone had a profound effect on fungal growth and development, including asexual reproduction, germination and appressorium formation in M. oryzae. Such defects in pre-penetration development resulted in complete loss of pathogenicity in the deletion mutant. Furthermore, genetic analysis of MoSAS3 and MoGCN5 encoding a Gcn5-related N-acetyltransferase family histone acetyltransferase suggested that two conserved components of histone acetylation are integrated differently into epigenetic regulatory mechanisms in the yeast and a filamentous fungus. RNA-seq analysis of ΔMosas3 showed two general trends: many DNA repair and DNA damage response genes are up-regulated, while carbon and nitrogen metabolism genes are down-regulated in ΔMosas3. Our work demonstrates the importance of MYST family histone acetyltransferase as a developmental regulator and illuminates a degree of functional variation in conserved catalytic subunits among different fungal species.

Keywords: MoSAS3; development; histone acetyltransferase; pathogenicity; rice blast.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Epistasis, Genetic
  • Fungal Proteins / metabolism*
  • Gene Deletion
  • Gene Expression Regulation, Fungal
  • Gene Ontology
  • Histone Acetyltransferases / chemistry
  • Histone Acetyltransferases / metabolism*
  • Hyphae / growth & development
  • Magnaporthe / enzymology
  • Magnaporthe / genetics
  • Magnaporthe / growth & development*
  • Magnaporthe / pathogenicity*
  • Oryza / microbiology*
  • Plant Diseases / microbiology*
  • Protein Domains
  • Reproduction, Asexual
  • Spores, Fungal / growth & development

Substances

  • Fungal Proteins
  • Histone Acetyltransferases