METTL3/METTL14 maintain human nucleoli integrity by mediating SUV39H1/H2 degradation

Nat Commun. 2024 Aug 21;15(1):7186. doi: 10.1038/s41467-024-51742-7.

Abstract

Nucleoli are fundamentally essential sites for ribosome biogenesis in cells and formed by liquid-liquid phase separation (LLPS) for a multilayer condensate structure. How the nucleoli integrity is maintained remains poorly understood. Here, we reveal that METTL3/METTL14, the typical methyltransferase complex catalyzing N6-methyladnosine (m6A) on mRNAs maintain nucleoli integrity in human embryonic stem cells (hESCs). METTL3/METTL14 deficiency impairs nucleoli and leads to the complete loss of self-renewal in hESCs. We further show that SUV39H1/H2 protein, the methyltransferases catalyzing H3K9me3 were dramatically elevated in METTL3/METTL14 deficient cells, which causes an accumulation and infiltration of H3K9me3 across the whole nucleolus and impairs the LLPS. Mechanistically, METTL3/METTL14 complex serves as an essential adapter for CRL4 E3 ubiquitin ligase targeting SUV39H1/H2 for polyubiquitination and proteasomal degradation and therefore prevents H3K9me3 accumulation in nucleoli. Together, these findings uncover a previously unknown role of METTL3/METTL14 to maintain nucleoli integrity by facilitating SUV39H1/H2 degradation in human cells.

MeSH terms

  • Cell Nucleolus* / metabolism
  • HEK293 Cells
  • Histone-Lysine N-Methyltransferase
  • Histones / metabolism
  • Human Embryonic Stem Cells / metabolism
  • Humans
  • Methyltransferases* / genetics
  • Methyltransferases* / metabolism
  • Proteolysis
  • Repressor Proteins* / genetics
  • Repressor Proteins* / metabolism
  • Ubiquitin-Protein Ligases / genetics
  • Ubiquitin-Protein Ligases / metabolism
  • Ubiquitination

Substances

  • Methyltransferases
  • METTL3 protein, human
  • SUV39H1 protein, human
  • METTL14 protein, human
  • Repressor Proteins
  • Histones
  • SUV39H2 protein, human
  • Ubiquitin-Protein Ligases
  • Histone-Lysine N-Methyltransferase