The modification landscape of P. aeruginosa tRNAs

  1. Pedro J Batista1,4
  1. 1 Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health;
  2. 2 Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.;
  3. 3 Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, National Institues of Health
  1. * Corresponding author; email: pedro.batista{at}nih.gov

Abstract

RNA modifications have a substantial impact on tRNA function, with modifications in the anticodon loop contributing to translational fidelity and modifications in the tRNA core impacting structural stability. In bacteria, tRNA modifications are crucial for responding to stress and regulating the expression of virulence factors. Although tRNA modifications are well-characterized in a few model organisms, our knowledge of tRNA modifications in human pathogens, such as Pseudomonas aeruginosa, remains limited. Here we leveraged two orthogonal approaches to build a reference landscape of tRNA modifications in E. coli, which enabled us to identify similar modifications in P. aeruginosa. Our analysis revealed a substantial degree of conservation between the two organisms, while also uncovering potential sites of tRNA modification in P. aeruginosa tRNAs that are not present in E. coli. The mutational signature at one of these sites, position 46 of tRNAGln1(UUG) is dependent on the P. aeruginosa homolog of TapT, the enzyme responsible for the 3-(3-amino-3-carboxypropyl) uridine (acp3U) modification. Identifying which modifications are present on different tRNAs will uncover the pathways impacted by the different tRNA modifying enzymes, some of which play roles in determining virulence and pathogenicity.

Keywords

  • Received February 26, 2024.
  • Accepted April 9, 2024.

This is a work of the US Government.

ACCEPTED MANUSCRIPT

This Article

  1. RNA rna.080004.124 Published by Cold Spring Harbor Laboratory Press for the RNA Society

Article Category

ORCID

Share