Overexpression of Leishmania major protein arginine methyltransferase 6 reduces parasite infectivity in vivo

Acta Trop. 2023 Aug:244:106959. doi: 10.1016/j.actatropica.2023.106959. Epub 2023 May 29.

Abstract

Arginine methylation is catalysed by Protein Arginine Methyltransferases (PRMTs) and can affect how a target protein functions and how it interacts with other macromolecules, which in turn impacts on cell metabolism and gene expression control. Leishmania parasites express five different PRMTs, and although the presence of each individual PRMT is not essential per se, the imbalanced activity of these PRMTs can impact the virulence of Leishmania parasites in vitro and in vivo. Here we created a Leishmania major cell line overexpressing PRMT6 and show that similar to what was observed for the T. brucei homologous enzyme, L. major PRMT6 probably has a narrow substrate range. However, its overexpression notably impairs the infection in mice, with a mild reduction in the number of viable parasites in the lymph nodes. Our results indicate that arginine methylation by LmjPRMT6 plays a significant role in the adaptation of the parasite to the environment found in the mammalian host.

Keywords: Arginine methylation; In vivo infection; Leishmania; Protein arginine methyltransferase.

MeSH terms

  • Animals
  • Arginine / metabolism
  • Leishmania major*
  • Mammals
  • Methylation
  • Mice
  • Parasites* / metabolism
  • Protein-Arginine N-Methyltransferases / chemistry
  • Protein-Arginine N-Methyltransferases / genetics
  • Protein-Arginine N-Methyltransferases / metabolism

Substances

  • Protein-Arginine N-Methyltransferases
  • Arginine