OsALKBH9‐mediated m6A demethylation regulates tapetal PCD and pollen exine accumulation in rice

Summary The N 6 ‐methyladenosine (m 6 A) mRNA modification is crucial for plant development and stress responses. In rice, the male sterility resulting from the deficiency of OsFIP37, a core component of m 6 A methyltransferase complex, emphasizes the significant role of m 6 A in male fertility. m 6 A is reversible and can be removed by m 6 A demethylases. However, whether mRNA m 6 A demethylase regulates male fertility in rice has remained unknown. Here, we identify the mRNA m 6 A demethylase OsALKBH9 and demonstrate its involvement in male fertility regulation. Knockout of OsALKBH9 causes male sterility, dependent on its m 6 A demethylation activity. Cytological analysis reveals defective tapetal programmed cell death (PCD) and excessive accumulation of microspores exine in Osalkbh9‐1 . Transcriptome analysis of anthers shows up‐regulation of genes involved in tapetum development, sporopollenin synthesis, and transport pathways in Osalkbh9‐1 . Additionally, we demonstrate that OsALKBH9 demethylates the m 6 A modification in TDR and GAMYB transcripts, which affects the stability of these mRNAs and ultimately leads to excessive accumulation of pollen exine. Our findings highlight the precise control of mRNA m 6 A modification and reveal the pivotal roles played by OsALKBH9‐mediated m 6 A demethylation in tapetal PCD and pollen exine accumulation in rice.