Transfer RNA modification and infection - Implications for pathogenicity and host responses

Biochim Biophys Acta Gene Regul Mech. 2018 Apr;1861(4):419-432. doi: 10.1016/j.bbagrm.2018.01.015. Epub 2018 Jan 31.

Abstract

Transfer RNA (tRNA) molecules are sumptuously decorated with evolutionary conserved post-transcriptional nucleoside modifications that are essential for structural stability and ensure efficient protein translation. The tRNA modification levels change significantly in response to physiological stresses, altering translation in a number of ways. For instance, tRNA hypomodification leads to translational slowdown, disrupting protein homeostasis and reducing cellular fitness. This highlights the importance of proper tRNA modification as a determinant for maintaining cellular function and viability during stress. Furthermore, the expression of several microbial virulence factors is induced by changes in environmental conditions; a process where tRNA 2-thiolation is unequivocal for pathogenicity. In this review, we discuss the multifaceted implications of tRNA modification for infection by examining the roles of nucleoside modification in tRNA biology. Future development of novel methods and combinatory utilization of existing technologies will bring tRNA modification-mediated regulation of cellular immunity and pathogenicity to the limelight.

Keywords: Host-pathogen interaction; Infection; Post-translational modification; Stress; Transfer RNA.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adaptation, Physiological / genetics
  • Animals
  • Anticodon / genetics
  • Codon / genetics
  • Genetic Code
  • Host-Pathogen Interactions / genetics*
  • Humans
  • Infections / genetics*
  • Infections / physiopathology
  • Metabolic Networks and Pathways / physiology
  • Models, Molecular
  • Nucleic Acid Conformation
  • Oxidative Stress / genetics
  • Protein Biosynthesis
  • RNA Processing, Post-Transcriptional*
  • RNA Stability
  • RNA, Transfer / chemistry
  • RNA, Transfer / genetics
  • RNA, Transfer / metabolism*
  • RNA-Directed DNA Polymerase / metabolism
  • Ribosomes / metabolism
  • Stress, Physiological / genetics
  • Sulfur / metabolism
  • Virulence / genetics*

Substances

  • Anticodon
  • Codon
  • Sulfur
  • RNA, Transfer
  • RNA-Directed DNA Polymerase