TMK4-mediated FIP37 phosphorylation regulates auxin-triggered N 6 -methyladenosine modification of auxin biosynthetic genes in Arabidopsis.

The dynamics of N ⁶ -methyladenosine (m ⁶ A) mRNA modification are tightly controlled by the m ⁶ A methyltransferase complex and demethylases. Here, we find that auxin treatment alters m ⁶ A modification on auxin-responsive genes. Mechanically, TRANSMEMBRANE KINASE 4 (TMK4), a component of the auxin signaling pathway, interacts with and phosphorylates FKBP12-INTERACTING PROTEIN 37 (FIP37), a core component of the m ⁶ A methyltransferase complex, in an auxin-dependent manner. Phosphorylation of FIP37 enhances its interaction with RNA, thereby increasing m ⁶ A modification on its target genes, such as NITRILASE 1 (NIT1), a gene involved in indole-3-acetic acid (IAA) biosynthesis. 1-Naphthalacetic acid (NAA) treatment accelerates the mRNA decay of NIT1, in a TMK4- and FIP37-dependent manner, which leads to inhibition of auxin biosynthesis. Our findings identify a regulatory mechanism by which auxin modulates m ⁶ A modification through the phosphorylation of FIP37, ultimately affecting mRNA stability and auxin biosynthesis in plants.
Competing Interests: Declaration of interests The authors declare no competing interests.
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