4.6 Article

Histone Methylation Is Required for Virulence, Conidiation, and Multi-Stress Resistance of Alternaria alternata

Journal

FRONTIERS IN MICROBIOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2022.924476

Keywords

citrus brown spot; virulence; conidiation; Alternaria alternata; histone methylation

Categories

Funding

  1. Key Project for New Agricultural Cultivar Breeding in Zhejiang Province, China [2021C02066-1]
  2. Major Science and Technology R&D Program of Jiangxi Province [20194ABC28007]

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Histone methylation plays a critical role in transcriptional regulation and biological processes in eukaryotes. This study investigated the function of several histone methyltransferases (HMTs) and histone demethylases (HDMs) in the phytopathogenic fungus Alternaria alternata. The results showed that AaSet1 and AaSet2 are important for cell development, stress adaptation, and carbon source utilization in A. alternata. RNA-seq analysis revealed the regulatory mechanism of AaSet1 and AaSet2. Overall, this study provides genetic evidence for the central role of HMTs and HDMs in the functions of A. alternata.
Histone methylation, which is critical for transcriptional regulation and various biological processes in eukaryotes, is a reversible dynamic process regulated by histone methyltransferases (HMTs) and histone demethylases (HDMs). This study determined the function of 5 HMTs (AaDot1, AaHMT1, AaHnrnp, AaSet1, and AaSet2) and 1 HDMs (AaGhd2) in the phytopathogenic fungus Alternaria alternata by analyzing targeted gene deletion mutants. The vegetative growth, conidiation, and pathogenicity of increment AaSet1 and increment AaSet2 were severely inhibited indicating that AaSet1 and AaSet2 play critical roles in cell development in A. alternata. Multiple stresses analysis revealed that both AaSet1 and AaSet2 were involved in the adaptation to cell wall interference agents and osmotic stress. Meanwhile, increment AaSet1 and increment AaSet2 displayed serious vegetative growth defects in sole carbon source medium, indicating that AaSet1 and AaSet2 play an important role in carbon source utilization. In addition, increment AaSet2 colony displayed white in color, while the wild-type colony was dark brown, indicating AaSet2 is an essential gene for melanin biosynthesis in A. alternata. AaSet2 was required for the resistance to oxidative stress. On the other hand, all of increment AaDot1, increment AaHMT1, and increment AaGhd2 mutants displayed wild-type phenotype in vegetative growth, multi-stress resistance, pathogenicity, carbon source utilization, and melanin biosynthesis. To explore the regulatory mechanism of AaSet1 and AaSet2, RNA-seq of these mutants and wild-type strain was performed. Phenotypes mentioned above correlated well with the differentially expressed genes in increment AaSet1 and increment AaSet2 according to the KEGG and GO enrichment results. Overall, our study provides genetic evidence that defines the central role of HMTs and HDMs in the pathological and biological functions of A. alternata.

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