MTA1-mediated RNA m 6 A modification regulates autophagy and is required for infection of the rice blast fungus.
Zhiyong RenBozeng TangJunjie XingCaiyun LiuXuan CaiAhmed HendyMuhammad KamranHao LiuLu ZhengJunbing HuangXiao-Lin ChenPublished in: The New phytologist (2022)
In eukaryotes, N 6 -methyladenosine (m 6 A) is abundant on mRNA, and plays key roles in the regulation of RNA function. However, the roles and regulatory mechanisms of m 6 A in phytopathogenic fungi are still largely unknown. Combined with biochemical analysis, MeRIP-seq and RNA-seq methods, as well as biological analysis, we showed that Magnaporthe oryzae MTA1 gene is an orthologue of human METTL4, which is involved in m 6 A modification and plays a critical role in autophagy for fungal infection. The Δmta1 mutant showed reduced virulence due to blockage of appressorial penetration and invasive growth. Moreover, the autophagy process was severely disordered in the mutant. MeRIP-seq identified 659 hypomethylated m 6 A peaks covering 595 mRNAs in Δmta1 appressoria, 114 m 6 A peaks was negatively related to mRNA abundance, including several ATG gene transcripts. Typically, the mRNA abundance of MoATG8 was also increased in the single m 6 A site mutant ∆atg8/MoATG8 A982C , leading to an autophagy disorder. Our findings reveal the functional importance of the m 6 A methylation in infection of M. oryzae and provide novel insight into the regulatory mechanisms of plant pathogenic fungi.
Keyphrases
- rna seq
- genome wide
- single cell
- cell death
- endoplasmic reticulum stress
- signaling pathway
- oxidative stress
- dna methylation
- copy number
- transcription factor
- endothelial cells
- escherichia coli
- staphylococcus aureus
- binding protein
- pseudomonas aeruginosa
- antibiotic resistance genes
- gene expression
- biofilm formation
- genome wide identification
- nucleic acid
- microbial community
- genome wide analysis