MicroRNA-like milR236, regulated by transcription factor MoMsn2, targets histone acetyltransferase MoHat1 to play a role in appressorium formation and virulence of the rice blast fungus Magnaporthe oryzae

• Published in: Fungal genetics and biology Vol. 137; p. 103349
• Main Authors: Li, Ying, Liu, Xinyu, Yin, Ziyi, You, Yimei, Zou, Yibin, Liu, Muxing, He, Yanglan, Zhang, Haifeng, Zheng, Xiaobo, Zhang, Zhengguang, Wang, Ping
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-04-2020
• Subjects: Appressorium; MicroRNA-like RNA; Transcription factor; Virulence; Transcription factor; Appressorium; MicroRNA-like RNA; Virulence
• ISSN: 1087-1845; 1096-0937
• DOI: 10.1016/j.fgb.2020.103349

•MicroRNA-like milR236 targets the sequence encoding MoHat1.•milR236 overexpression induces delayed appressorium formation and virulence attenuation.•milR236 expression is regulated by the transcription factor MoMsn2.
MicroRNAs (miRNAs) play important roles in various cellular growth and developmental processes through post-transcriptional gene regulation via mRNA cleavage and degradation and the inhibition of protein translation. To explore if miRNAs play a role in appressoria formation and virulence that are also governed by the regulators of G-protein signaling (RGS) proteins in the rice blast fungus Magnaporthe oryzae, we have compared small RNA (sRNA) production between several ΔMorgs mutant and the wild-type strains. We have identified sRNA236 as a microRNA-like milR236 that targets the encoding sequence of MoHat1, a histone acetyltransferase type B catalytic subunit involved in appressorium function and virulence. We have also found that milR236 overexpression induces delayed appressorium formation and virulence attenuation, similar to those displayed by the ΔMohat1 mutant strain. Moreover, we have shown that the transcription factor MoMsn2 binds to the promoter sequence of milR236 to further suppress MoHAT1 transcription and MoHat1-regulated appressorium formation and virulence. In summary, by identifying a novel regulatory role of sRNA in the blast fungus, our studies reveal a new paradigm in the multifaceted regulatory pathways that govern the appressorium formation and virulence of M. oryzae.