TMK4-mediated FIP37 phosphorylation regulates auxin-triggered N6-methyladenosine modification of auxin biosynthetic genes in Arabidopsis

Cell Rep. 2024 Aug 27;43(8):114597. doi: 10.1016/j.celrep.2024.114597. Epub 2024 Aug 5.

Abstract

The dynamics of N6-methyladenosine (m6A) mRNA modification are tightly controlled by the m6A methyltransferase complex and demethylases. Here, we find that auxin treatment alters m6A 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 m6A methyltransferase complex, in an auxin-dependent manner. Phosphorylation of FIP37 enhances its interaction with RNA, thereby increasing m6A 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 m6A modification through the phosphorylation of FIP37, ultimately affecting mRNA stability and auxin biosynthesis in plants.

Keywords: CP: Molecular biology; CP: Plants.

MeSH terms

  • Adenosine* / analogs & derivatives
  • Adenosine* / metabolism
  • Arabidopsis Proteins* / genetics
  • Arabidopsis Proteins* / metabolism
  • Arabidopsis* / genetics
  • Arabidopsis* / metabolism
  • Gene Expression Regulation, Plant*
  • Indoleacetic Acids* / metabolism
  • Methyltransferases / genetics
  • Methyltransferases / metabolism
  • Phosphorylation
  • RNA Stability
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism

Substances

  • Indoleacetic Acids
  • Adenosine
  • Arabidopsis Proteins
  • N-methyladenosine
  • Methyltransferases
  • RNA, Messenger