Human TRMT112-Methyltransferase Network Consists of Seven Partners Interacting with a Common Co-Factor

Int J Mol Sci. 2021 Dec 18;22(24):13593. doi: 10.3390/ijms222413593.

Abstract

Methylation is an essential epigenetic modification mainly catalysed by S-Adenosyl methionine-dependent methyltransferases (MTases). Several MTases require a cofactor for their metabolic stability and enzymatic activity. TRMT112 is a small evolutionary conserved protein that acts as a co-factor and activator for different MTases involved in rRNA, tRNA and protein methylation. Using a SILAC screen, we pulled down seven methyltransferases-N6AMT1, WBSCR22, METTL5, ALKBH8, THUMPD2, THUMPD3 and TRMT11-as interaction partners of TRMT112. We showed that TRMT112 stabilises all seven MTases in cells. TRMT112 and MTases exhibit a strong mutual feedback loop when expressed together in cells. TRMT112 interacts with its partners in a similar way; however, single amino acid mutations on the surface of TRMT112 reveal several differences as well. In summary, mammalian TRMT112 can be considered as a central "hub" protein that regulates the activity of at least seven methyltransferases.

Keywords: RNA methylation; TRMT112; methyltransferase; protein stabilisation; ribosome biogenesis.

MeSH terms

  • Cell Line, Tumor
  • Enzyme Stability
  • HEK293 Cells
  • Humans
  • Methyltransferases / analysis
  • Methyltransferases / metabolism*
  • Models, Molecular
  • Protein Interaction Maps*

Substances

  • Methyltransferases
  • TRMT112 protein, human